http://raver-thelifeofahardcorepartyanimal.blogspot.com/

all about NRG 1 and NRG 2 AND NRG3

2010-06-15T18:28:00.001-07:00

NRG 1

Police have issued a warning about a new drug on the eve of the Scottish summer music festival season.

NRG-1 or Energy-1 has been marketed on websites as a legal high, but usually contains illegal Class B drugs and has already led to hospital admissions.

The warning comes as thousands of people head for the Rockness music festival near Inverness, which runs from today until Monday. T in the Park at Balado follows next month.

It comes after the criminalisation of Mephedrone, a drug marketed as a legal high which was then connected with the deaths of two teenagers.

Police said websites marketing NRG-1 claim it works as a stimulant, but users are experiencing extreme anxiety and hospitals have reported a number of admissions where individuals have required treatment after using the substance.

Some websites state that NRG-1 contains a substance called Napthepyrovalerone, also known as Naphyrone, which is not a controlled substance. However, to date, all samples of drugs labelled as NRG-1 that have been analysed were found to contain Class B drugs.

Detective Superintendent Willie MacColl, at the Scottish Crime and Drug Enforcement Agency, said: “We are aware of the emergence of the sale of a drug labelled NRG-1 being marketed as a substance that is not controlled, a so-called legal high.

“It is important that people understand the risks associated with such substances which are prepared and packaged in an unregulated manner.”

STAY AWAY FROM NRG 1 IT IS DEADLY AND VERY DANGEROUS NRG 2 AND NRG 3 AINT NOTHING LIKE NRG 1 THEY GIVE U A GOOD BUZZ BUT NRG 1 IS NASTY

THIS IS ALL ABOUT NRG 2 PICS AND KNOWLEDGE OF THE DRUG

2010-06-15T14:28:00.000-07:00

alot of you that have heard of NRG2 have said its rubbish with very little effects n alot of people ave sed it delivers a great buzz,not every single RC vendor sells the same batch,most sites cut these new substances to make alot of money,i know safe ones 2 get the stuff off and i aint had a problem yet,no problem they dont skank me when u get a gram theres a gram there it doesnt stick 2 the bag n shit,we all want pure drugs,were fed up of buyin on one site its shit n then next site its better why cant all sites sell the same substance why ave they gotta mess with the chemistry of these substances,watch who u get it off,alot of online vendors will try and rip u off always go for the cheap option and dont buy big lots unless uve tryed em before and u know that their quality is satisfactory,ive had a few batches of NRG 2 first lot i had tasted like really chemically not sweet made me gag i didnt wanna do much of it,n then next batch was a bit better bit sour and sweet and now the latest batch ive done is really sweet,no headaches no paronoia just a really nice buzz,im quite impressed with NRG 2 if i was raving i wud defo do that combined with ncat alot of people think they both da same i hope they aint both da same cos if they are it means weve been getting ripped off by vendors when we fink its a new substance when all it is is the name has been changed to sommin else so people will buy it,NRG 2 is stronger than ncat thats for sure ive only had 2 batchs of ncat n done em both in 2 days like not good,it must of been that shit,cos i never overdo drugs fuck dat stuff,these are pure chemicals that are 99.88% purity,so they aint cut at all but there are ones dat are,u will kno if they are cut they will burn ur throat really bad u will get constant headaches ur heart will go 2 fast,it will taste like really chemically or acidly and wen u swallow it u will keep swallowing,if u keep doing that,thats a warning sign so bare that in mind,also u mite get very bad eye coordination and wont be able to concentrate and u will get paronoid u mite go really quiet that can also be known as u cud overdose,another word for it is sledging when i used 2 do speed it made me really quiet n all felt like i was gonna collapse it was so scary im glad i gave it up speed is an evil powerful drug that will control u if u let it,i advise everyone to pace themselves on any drug and find out as much knowledge as u can b4 u touch any substance,and never let the drug control you,u control the drug,

this is pure NRG 2 if u get it like dis then dis is what it shud look like if it has any sort

of sandy colour or any colour to it instead of white then its either cut or being sold as

sommin else so be careful,

ALL THIS IS ABOUT NRG 2 PEOPLE ITS LONG TOOK ME AGES 2 FIND DIS

The Neuregulin family of ligands and their receptors, the Erbb tyrosine kinases, have important roles in epidermal and mammary gland development as well as during carcinogenesis. Previously, we demonstrated that Neuregulin3 (Nrg3) is a specification signal for mammary placode formation in mice. Nrg3 is a growth factor, which binds and activates Erbb4, a receptor tyrosine kinase that regulates cell proliferation and differentiation. To understand the role of Neuregulin3 in epidermal morphogenesis, we have developed a transgenic mouse model that expresses Nrg3 throughout the basal layer (progenitor/stem cell compartment) of mouse epidermis and the outer root sheath of developing hair follicles.

Results

Transgenic females formed supernumerary nipples and mammary glands along and adjacent to the mammary line providing strong evidence that Nrg3 has a role in the initiation of mammary placodes along the body axis. In addition, alterations in morphogenesis and differentiation of other epidermal appendages were observed, including the hair follicles. The transgenic epidermis is hyperplastic with excessive sebaceous differentiation and shows striking similarities to mouse models in which c-Myc is activated in the basal layer including decreased expression levels of the adhesion receptors, α6-integrin and β1-integrin.

Conclusion

These results indicate that the epidermis is sensitive to Nrg3 signaling, and that this growth factor can regulate cell fate of pluripotent epidermal cell populations including that of the mammary gland. Nrg3 appears to act, in part, by inducing c-Myc, altering the proliferation and adhesion properties of the basal epidermis, and may promote exit from the stem cell compartment. The results we describe provide significant insight into how growth factors, such as Nrg3, regulate epidermal homeostasis by influencing the balance between stem cell renewal, lineage selection and differentiation.

Background

Neuregulins are a family of ligands that signal through the four Erbb receptor tyrosine kinases to activate pathways. This network mediates a wide range of processes that have relevance to both developmental processes and cancer, including cell adhesion, differentiation, proliferation, migration and death [1]. Our previous studies suggested that Nrg3 signaling acts to promote the initiation of mammary placode development [2]. The cognate receptor for Nrg3, Erbb4, is required for terminal differentiation of the mammary gland and lactation fails in its absence [3,4]. Impaired mammary epithelial proliferation and lobuloalveolar defects are also observed in Nrg1α-null mice [5]. Analysis of Amphiregulin-null mice demonstrated the requirement of Amphiregulin for ductal outgrowth at puberty [6]. Studies of compound null mutations for genes for the Egf-related ligands (Amphiregulin, Egf, and Tgfα) demonstrated failed lactation due to abnormal alveolar development and differentiation, whereas no lactation defect is apparent when these genes are singly mutated [6]. Studies of mammary tissue from Erbb1 and Erbb2-null mouse models have shown that these genes have important roles in mammary ductal outgrowth/morphogenesis [7-10]. Mouse models which overexpress the ligand, Nrg1, or the Erbb2 receptor (both wild-type and activated forms) display severe hyperplastic epidermal and/or mammary phenotypes depending on the cell type specificity of promoter used to drive transgene expression [11-15]. These mouse models have provided a useful framework for understanding how this ligand/receptor network acts to promote differentiation, outgrowth, and carcinogenesis of epithelial tissues.

Egf and Egf-like ligands that signal through Egfr were initially discovered and named due to their profound effects on epidermal development [16-18]. Egf increases epidermal thickness and cellularity and stimulates proliferation of epidermal keratinocytes [16]. Mice with targeted disruptions of Egfr/Erbb1 are usually embryonically lethal but this is strain-dependent, so it is possible to analyze hypomorphs, and viable strains display epithelial hypoplasia [19-21]. Mice harbouring the Waved-2 allele of Egfr develop abnormal hair that appears wavy and also display a mild lactation defect [22]. Other Egf-like ligands expressed by keratinocytes include Amphiregulin [23], Betacellulin [24], Heparin-binding Egf-like growth factor [25], and TGFα [26]. Using wound healing models, Nrg1/Heregulin (HRG) has been implicated in epithelial migration and differentiation [27]. The Nrg1 isoforms, HRGα and HRGβ, elicit different effects in cultured keratinocytes [28]; HRGα acts as a potent motility factor whereas HRGβ has no effect on migration in wound healing assays [27,28]. In contrast, in normal melanocytes, HRGβ significantly enhances cell migration, but not proliferation, while HRGα has no effect on migration or cell growth of normal melanocytes [29]. Despite the profound biological effects that Egf-like ligands elicit, their modes of action are not yet fully understood, particularly with respect to their ability to regulate cell fate and lineage commitment.

Mammary placodes are thought to arise as a result of local cell migration [30] and early stages are characterized by epithelial stratification [31,32]. Our previous studies indicated that Nrg3 promotes the differentiation of squamous epithelia into mammary epithelia [2]. In the mouse embryo, Nrg3 appears to regulate epithelial stratification or local epithelial aggregations at the sites that mammary placodes will form. Mice harbouring the ska mutation, a hypomorphic allele of Nrg3, often fail to form placode three; this can be restored after culture with recombinant Nrg3-Egf. Placode morphogenesis is governed by molecules that alter cell adhesion dynamics and, in some cases, proliferation of pluripotent epithelial cells [33,34]. In the mammary gland, as with the development of all epidermal appendages, undifferentiated stem cells are committed to specific lineages and a population of cells with a high capacity for proliferation is delimited, which subsequently differentiates [33,35,36]. The role of Nrg3 signaling in the determination of epidermal stem cell fate remains largely uncharacterized. Therefore, we developed a mouse model to examine the outcome of ectopic expression of Nrg3 in the basal layer of the developing epithelia under the control of the Keratin14 (K14) promoter. This promoter results in expression beyond the normal spatial and temporal domains of Nrg3 expression into the stem cell compartment. Expression of Nrg3 in the basal layer of the epidermis resulted in alterations in a variety of epidermal organs including the skin, hair follicles, sebaceous glands, external genitalia and mammary glands. Analysis of epithelial differentiation and progenitor markers suggests that differentiation of progenitor cell populations is profoundly altered by Nrg3 expression.

Results

Nrg3 is expressed in the developing epidermis and hair follicles

We have shown previously, using both in situ hybridization and immunohistochemistry, that Nrg3 is expressed in the developing embryonic mouse epidermis from E12-E13 [2]. Nrg3 is also expressed in developing hair follicles at E14.5 (Fig. (Fig.1A).1A). To investigate Nrg3 expression in postnatal skin, we used immunohistochemistry on both frozen and fixed mouse epidermis (Fig. (Fig.1B1B and data not shown). We found that Nrg3 is expressed in the granular and cornified layers and in very few cells of the basal layer of the postnatal interfollicular epidermis, and at low to moderate levels in the hair follicles along the outer root sheath including the bulge and along the inner root sheath (Fig. (Fig.1B1B and Additional File 1).

Figure 1

Endogenous expression pattern of Nrg3, K14-Nrg3 transgene, and postnatal phenotype of a K14-Nrg3 founder mouse. (A) Nrg3 is expressed in the developing hair follicles at E14.5. Inset shows frozen section of the whole mount which confirmed the localization (more ...)

Ectopic expression of Nrg3 in the epidermis causes epidermal defects and early lethality

To extend the temporal and spatial range of Nrg3 expression in the epidermis, and determine whether Nrg3 can modulate the development of epidermis and its appendages, we generated transgenic mice expressing full-length Nrg3 from the human K14 promoter (Fig. (Fig.1C).1C). The K14 promoter is expressed in the periderm starting at E9.5 and, once stratified, in the basal layer (progenitor/stem cell compartment) of mouse epidermis and the outer root sheath of the hair follicles [37]. Founder mice were produced by pronuclear injection of the linearized transgene into fertilized eggs (Additional File 2). Levels of transgene expression in the epidermis of mice were determined by immunohistochemistry or by in situ hybridization (data not shown). Six male K14-Nrg3 transgenic founders exhibited a similar thickened, wrinkled, hairless phenotype that encompassed the entire skin of the animal (Fig. (Fig.1D).1D). Of these, four died a few days after birth or were unwell and were culled. However, two male founders expressing lower transgene levels were viable and exhibited hyperplastic epithelial phenotypes but did not display other epidermal appendage phenotypes, or the phenotypes were less severe. Furthermore, two male founder mice that were mosaic for transgene levels expressed variable levels of transgene expression and were also viable.

Histopathology of K14-Nrg3 transgenic skin

Histological examination of seven independent K14-Nrg3 transgenic founders revealed that the skin shared several unusual features. The epidermis displayed expanded suprabasal, granular and cornified layers when compared to non-transgenic littermates (Fig. 2A, B). Nucleated cells were present throughout the epidermis, even in the later differentiated compartments, except for the cornified layers, which were anucleate. An increase in the cellular density of the dermis was also observed. A large infiltration of fibroblasts was apparent and the fat layer appeared much thinner in the transgenic skin. Hair follicles were hyperplastic and mis-orientated within the dermis and sebaceous glands were mis-positioned and hyperplastic. All components of the hair follicle are present and differentiation proceeds normally but is disrupted at a very late stage so that the hair fiber either fails to form or when a fiber does form it does not penetrate through the thickened epithelium. However, mice derived from one lower expressing K14-Nrg3 transgenic line did form some sparse wavy hair but only one hair type (zigzag) was present compared to the four hair types normally found in non-transgenic littermates (Fig. 2C, D).

Figure 2

K14-Nrg3 transgenic mice display hyperplastic epithelia and hair follicleab normalities. Histological analysis of dorsal skin from K14-Nrg3 and age-matched non-transgenic littermate. (A) Skin section stained with H&E from non-transgenic littermate (more ...)

Using an antibody to the Egf domain of Nrg3, we detected Nrg3 expression in the basal, suprabasal, and granular layers of the epithelium and in the outer root sheath of hair follicles in the transgenic founder lines (Fig. (Fig.2E).2E). Cytoplasmic and membrane staining is observed suggesting that both membrane-spanning and secreted forms of Nrg3 are produced in the transgenic K14-Nrg3 mice, as expected from the isoform of Nrg3 present in the K14-Nrg3 construct. Non-transgenic littermates express Nrg3 in a few basal and in the granular and cornified layers and low to moderate levels throughout the hair follicles (Fig. (Fig.1B1B).

Altered Erbb receptor activation is observed in K14-Nrg3 transgenic skin

Erbb1, Erbb2, and Erbb3 expression has been reported in both human and mouse skin [15,38,39]. Erbb4 expression has not been reported in postnatal mouse epidermis although expression has been observed in both embryonic and adult human skin [38]. Erbb4 is expressed in the epithelia of the developing mammary placode from the time it is morphologically distinct [2]. We examined expression of the four Erbb receptors in both transgenic and non-transgenic postnatal skin. Erbb1 and Erbb2 are expressed in the basal epithelia and differentiating epidermal layers and in the outer root sheath of the hair follicles of both non-transgenic and transgenic skin (Fig. 3A–D). Erbb3 is expressed in the basal, suprabasal layers and at higher levels in the granular epithelial layers and in the outer root sheath of the hair follicles of both transgenic and non-transgenic skin (Fig. 3E, F). In non-transgenic mouse epidermis, we detect only very low levels of Erbb4 in the interfollicular epidermis and we observed low levels of expression in the hair follicles (Fig. (Fig.3G3G and Additional File 1). However, in K14-Nrg3 transgenic skin, we observed significantly increased levels of Erbb4 in the epidermis (mainly cytosolic and weak membranous) (Fig. (Fig.3H),3H), which suggest that Nrg3 expression in the basal epithelia might induce an autocrine signaling loop.

Figure 3

Expression and activation of Erbb receptors in dorsal epidermis from non-transgenic and K14-Nrg3 transgenic littermates at P7. (A, C, E, G) Skin from non-transgenic littermate. (B, D, F, H) Skin from K14-Nrg3 transgenic founder. (A and B) Erbb1 is expressed (more ...)

We explored the signaling events that mediate the Nrg3 response in the epidermis. Erbb1 is slightly more activated in the transgenic epidermis when compared to the non-transgenic epidermis (Fig. (Fig.3I).3I). Both Erbb2 and Erbb3 activation levels are similar in the transgenic and non-transgenic epidermis (Fig. (Fig.3I).3I). Ectopic Nrg3 promotes a slight increase in the levels of Erbb4 and a moderate increase in tyrosine phosphorylation of Erbb4 in the transgenic epidermis (Fig. (Fig.3I).3I). The possible active signaling complexes in the transgenic epidermis are therefore Erbb1:1, Erbb1:2, Erbb1:3, Erbb2:3, Erbb2:4, Erbb4:4 since Erbb2 requires a Neuregulin binding receptor to signal and Erbb3 homodimers are inactive.

Signaling through the Erbb4 receptor is complicated as four major variants of the receptor exist [40]. Alternative splice variants of Erbb4 are produced at two distinct sites resulting in four possible isoforms of the receptor. JM-a and JM-b variants encode variable extracellular juxtamembrane isoforms that can be cleaved by matrix metalloproteases (MMPs) (JM-a) or are resistant to such cleavage (JM-b) [41]. Two cytoplasmic variants also exist which contain (CYT-1) or lack (CYT-2) an exon corresponding to sixteen amino acids that encodes a phosphatidylinositol 3-kinase (PI3K) docking site [42]. We examined the expression of Erbb4 isoforms in the epidermis of three independent K14-Nrg3 transgenic lines and compared them to the epidermis from non-transgenic siblings. CYT-1 and CYT-2 isoforms were expressed at similar levels in both the transgenic and non-transgenic epidermis (Fig. (Fig.3J).3J). We found that unusual Erbb4 JM isoform profiles exist in the transgenic epidermis that are distinct from those expressed in non-transgenic epidermis. Similar levels of the JM-a and JM-b isoforms are expressed in non-transgenic epidermis. We observed deviations such that either JM-a or JM-b isoforms were preferentially expressed in the transgenic lines (Fig. (Fig.3J).3J). These results suggest that misexpressing Nrg3 in the epidermis alters the ratios of Erbb4 JM splice isoform gene expression.

The JM-a domain of Erbb4 encodes a cleavable receptor which can transmit signals to the cytoplasm and nucleus [43-45]. Binding of Nrg1 to the Erbb4 JM-a ectodomain isoform results in the cleavage and shedding of the 120 kD ectodomain. This is mediated by tumor necrosis factor-alpha converting enzyme and results in the production of an 80 kD intracellular membrane-bound domain [46]. This domain can then be cleaved by gamma-secretase to release an 80 kD intracellular domain [47]. Immunoprecipitate analysis of Erbb4 receptor signaling detected no activated 80 kD isoform in the epidermis from transgenic or non-transgenic littermates (Fig. (Fig.3I).3I). Therefore, activated Erbb4 exists predominantly in the 180 kD membrane-bound isoform in the epidermis of both transgenic and non-transgenic littermates (Fig. (Fig.3I3I).

K14-Nrg3 transgenic mice exhibit other epithelial appendage phenotypes

We observed fewer K14-Nrg3 transgenic females than predicted and the overall efficiency of transgenesis was low (Additional File 3), suggesting that ectopic expression of Nrg3 in the epidermis during embryogenesis may be partially lethal, particularly in females. Four female transgenic founders with obvious skin phenotypes were obtained. Of these, two were found dead shortly after birth. Histological analysis showed a skin phenotype similar to that observed in the other male transgenic founders (data not shown). The other two female founders both displayed a hairless, wrinkled, thickened, pale skin similar to that observed in the male founders except this was present on approximately half of the body of the mouse, consistent with integration of the transgene at the two-cell stage (Additional File 4).

At P12, these two female founders were scored for the number and placement of nipples on the ventral surface. In both females, in addition to the 5 pairs in the normal location (Fig. (Fig.4A),4A), there were multiple ectopic nipples both along the "mammary line" and also in adjacent locations (Fig. 4B, C). Results from breeding from these females were consistent with chimerism. The one transgenic male pup produced in the first litter displayed the same hairless, wrinkled, thickened, pale skin phenotype (over its entire body surface) shared by the other transgenic founder males and died at P5. The female founder mice were culled to collect tissue samples for analysis and verify that mammary tissue (fat pad and epithelial ducts) was associated with the ectopic nipples (Fig. 4E, F, G, H). Ectopic nipples observed on transgenic mice are usually smaller than the endogenous nipples which are very large when compared to non-transgenic nipples (Fig. 4D, E) but varied considerably in size and are sometimes as large as the endogenous transgenic nipples (Fig. 4I, J). Both endogenous and ectopic nipples express Keratin2e, a nipple marker for mouse nipple epidermis [48] (Fig. 4I, J).

Figure 4

Ectopic expression of Nrg3 in the epidermis results in the formation of ectopic nipples and mammary glands. (A) Ventral surface of non-transgenic littermate at P12 with the five pairs of nipples marked. Numbers denote the positions of the five normal (more ...)

Both male and female mice exhibited enlarged external genitalia when compared to non-transgenic littermates (Fig. 4A, B and Fig. 5A, B). Despite the increased size of the external genitalia, most mice were fertile and could breed. Most transgenic founders displayed very sparse and wispy whiskers and one line eventually grew sparse and wavy hair (Fig. 5C, D). Clusters of hair follicles were observed in some skin sections, which is indicative of abnormal patterning events (Fig. 5E, F). One transgenic founder line exhibited premature tooth eruption (culled at P7 as it could no longer suckle) but normal tooth number and cusp patterning were observed in these and other transgenic founder lines (data not shown).

Figure 5

Ectopic expression of Nrg3 in the epidermis causes defects in the external genitalia, vibrissae, and hair. (A) External genitalia of male non-transgenic littermate is indicated with an arrow. (B) Enlarged external genitalia of K14-Nrg3 transgenic male (more ...)

Hyperproliferative marker profile but a normal terminal differentiation profile observed in K14-Nrg3 transgenic interfollicular epidermis

The status of epidermal differentiation was assessed using immunohistochemistry of paraffin sections. Although the epidermis is thicker in K14-Nrg3 skin compared to non-transgenic littermates, markers of terminal epidermal differentiation were present. The distribution of Filaggrin, a terminal differentiation marker, is maintained in the granular and cornified layers (Fig. 6A, B). Similarly Involucrin, another terminal differentiation marker is also expressed in the granular and cornified layers (Additional File 5). The distribution of K1 and K10, markers for committed early differentiating cells, are unaltered and remain in the suprabasal layer (Fig. 6C, D; Additional File 5). Neoplastic skin lesions generally display reduced K1 expression so the transgenic epidermis does not appear to be neoplastic. K5 and K14 were used as markers for the basal proliferating keratinocytes and showed markedly altered expression. Both were expressed at high levels throughout the basal and suprabasal layers of K14-Nrg3 transgenic skin (Fig. 6E, F; Additional File 5). Another basal keratin, K15 is normally restricted to basal keratinocytes as observed in non-transgenic littermates (Fig. (Fig.6G)6G) and marks undifferentiated cells with low turnover [49]. K15 expression is reduced in the basal interfollicular epidermis in K14-Nrg3 basal epidermis (Fig. (Fig.6H).6H). K15 expression is retained in the outer root sheath where it marks the bulge region of the hair follicle in both normal and mutant epidermis (Fig. 6G, H) [50]. K15 expression is not compatible with keratinocyte activation and is frequently downregulated in hyperproliferative conditions [51]. The large expansion of suprabasal and granular layers observed in transgenic skin is also a feature of hyperproliferating conditions. Ectopic expression of Nrg3 in the basal layer deregulates the expression pattern of keratin markers, K5, K14, and K15 to one associated with hyperproliferation conditions. The terminal differentiation program of keratinocytes in K14-Nrg3 transgenic skin is essentially normal and characterized by excessive production of terminally differentiated cells.

Figure 6

Immunohistochemistry using epidermal differentiation markers. Immunohistochemistry of sections of dorsal skin from transgenic mice and non-transgenic littermates at P7 with antibodies to the proteins indicated. (A and B) Expression of Filaggrin, a terminal (more ...)

Nrg3 signaling stimulates epidermal proliferation

The increased thickness of the epidermis suggested that Nrg3 stimulates proliferation. Ki67 was used as a proliferation marker for cells (expressed by cells in late G1, S, G2, and M phases). In contrast to normal skin (Fig. (Fig.7A),7A), the K14-Nrg3 basal cells are nearly all Ki67+ and many suprabasal cells are Ki67+ (Fig. (Fig.7B).7B). In one K14-Nrg3 transgenic line, approximately 43% of the interfollicular epithelial cells are Ki67+ compared to 26% observed in non-transgenic littermates in postnatal day 7 skin (Fig. (Fig.7C).7C). Normally, a restricted number of basal cells express CyclinD1 (which is expressed by cells in G1 phase) (Fig. (Fig.7D).7D). However, CyclinD1 expression is observed in the basal, suprabasal, and granular cell layers of K14-Nrg3 epidermis (Fig. (Fig.7E).7E). Therefore, constitutive expression of Nrg3 increases the number of cycling cells in the epidermis, including the basal layer.

Figure 7

Increased proliferation in K14-Nrg3 epidermis. Immunohistochemical analysis shows an increase in Ki67 and CyclinD1 in the epidermis. (A and B) In non-transgenic epidermis (A), Ki67 is restricted to some basal cells. In K14-Nrg3 skin (B), Ki67 is expressed (more ...)

Sustained Nrg3 signaling stimulates sebocyte differentiation

To examine the differentiation of sebaceous glands, we stained transgenic and non-transgenic skin with Oil Red O, which marks lipid- containing cells, including sebocytes. In normal skin, sebaceous glands were associated with the upper part of each hair follicle (Fig. (Fig.8A).8A). In K14-Nrg3 transgenic skin, the number and size of sebocytes was greatly increased (Fig. (Fig.8B).8B). This is especially dramatic in skin samples collected from older mice, where essentially all of the abnormal hair follicles are filled with sebocytes and only few structures resembling hair follicles remain (Fig. (Fig.8D).8D). This suggests that Nrg3 signaling stimulates sebocyte differentiation. Several studies have shown that c-Myc activation stimulates sebocyte differentiation [52,53], and therefore we examined c-Myc expression. We found that K14-Nrg3 transgenic skin exhibited increased c-Myc expression through most of the basal layer when compared to non-transgenic littermates (Fig. 8E, F). Western blot analysis confirmed an increase in the levels of c-Myc in K14-Nrg3 transgenic skin compared to non-transgenic littermates (Fig. (Fig.8G8G)

Figure 8

Nrg3 signaling stimulates sebocyte differentiation. (A and B) In non-transgenic epidermis (A), Oil Red O stains the sebaceous gland (indicated by arrows) associated with each hair follicle. In K14-Nrg3 skin (B), the sebaceous glands (indicated by arrows) (more ...)

Sustained Nrg3 signaling perturbs basement membrane organization

The extracellular matrix receptor, β1-integrin, is preferentially expressed in many epidermal stem cells and thought to be required to maintain the stem cell compartment. β1-integrin exhibits reduced staining in K14-Nrg3 epidermis when compared to non-transgenic littermates (Fig. 9A, B). The hemidesmosomal component, α6-integrin [54], also displayed reduced staining in K14-Nrg3 epidermis when compared to non-transgenic littermates (Fig. 9C, D, E, F). Strong adhesion of the basal cells to the underlying basal lamina is provided by the hemidesmosomes. The aberrant staining of cell adhesion markers, α6-integrin and β1-integrin, suggest that partial dissolution of underlying basement membrane has occurred. Tenascin-C, an adhesion-modulating extracellular matrix glycoprotein, is expressed along the basement membrane in the vicinity of hair follicles in normal epidermis (Fig. (Fig.9G).9G). There is significant upregulation of Tenascin-C within the basement membrane of K14-Nrg3 skin (Fig. (Fig.9H9H).

Figure 9

Nrg3 signaling perturbs the expression of basement membrane components and stem cell markers. (A and B) β1-integrin is expressed along the basement membrane (indicated by an arrow) throughout the basal epidermis of non-transgenic littermate (A). (more ...)

Nrg3 activity regulates the fate of epidermal progenitor cells

p63 is normally expressed in most basal epidermal cells and some suprabasal cells and is thought to act to maintain the proliferative potential of stem cells and to mediate epidermal differentiation [55-57]. p63 is expressed in cells with high proliferative potential and is absent in cells undergoing terminal differentiation. We observed expanded expression of p63 which was detected in up to four suprabasal cell layers in K14-Nrg3 epidermis. (Fig. 9I, J). A similar distribution of Ki67+ and p63+ cells was observed in the suprabasal layers (compare Figs Figs9J9J and and7B).7B). By definition, stem cells rarely cycle and the transit-amplifying cells are actively cycling [58]. This suggests that an increased number of quiescent stem cells are recruited into cell cycle and enter into the transit-amplifying compartment in K14-Nrg3 epidermis. Transit-amplifying cells divide several times to produce differentiated cells, which leads to terminal differentiation along various lineages. These results suggest that Nrg3 can influence epidermal stem cell fate decisions and, when ectopically expressed in the basal epidermis, Nrg3 promotes the differentiation of stem cells into epidermal and sebaceous lineages and not along the hair lineage.

Discussion

We have shown that sustained expression of Nrg3 in the basal epidermis alters the development of epidermal organs including the skin, hair, and mammary glands (Figs (Figs1,1, ,2,2, ,4).4). Modulation of Nrg3 signaling affects the number of mammary glands by promoting initiation. We have not observed the induction of other ectopic organs in the K14-Nrg3 founders aside from mammary glands. However, ectopic Nrg3 did increase the size and alter the shape of most epithelial appendages, which is suggestive of morphogenetic changes. Failure of proper hair differentiation occurred and, in the few cases where hair fibers formed and emerged, only one hair type, zigzag, developed (Fig. (Fig.2).2). Our observation of clusters of hair follicles suggests that in some regions, normal patterning is perturbed (Fig. (Fig.5F).5F). In skin from older transgenic mice, the entire hair follicle structure is filled with sebocytes suggesting alterations in cell fate decisions have occurred (Fig. (Fig.8D8D).

K14-Nrg3 transgenic mice form extra nipples associated with mammary ducts (Fig. (Fig.4).4). The extra mammary glands develop along and close to the mammary line. Although K14 is expressed in the epidermis from E9.5, it is not upregulated until E14.5 when strong K14 expression is observed in the basal layer of the epidermis, in the outer root sheath and in the bulge cells [37]. K14 upregulation therefore occurs after the mammary placodes have already formed. Our K14-Nrg3 transgenics were low copy number integrants and expressed low-levels of the transgene and it is possible that higher levels of expression might elicit other phenotypic effects if it were not lethal. Our previous studies demonstrated both epidermal stratification (the first indication of mammary placode development) and placode formation adjacent to sites of ectopically delivered recombinant Nrg3-Egf domain in mouse embryo explant cultures [2]. The results reported here suggest that, at least in some cases, these ectopic placodes have the ability to complete the entire mammary morphogenetic program.

All four Erbb receptors are expressed in the developing mouse epidermis providing a wide range of signaling possibilities as well as compensatory mechanisms (Fig. (Fig.3).3). Depending on the ligand and the availability of dimerization partners these receptors will then transmit quantitatively or qualitatively different signals in different cell types [59,60]. No significant elevations in Egfr, Erbb2, or Erbb3 were observed as assessed by immunohistochemistry and western blot (Fig. (Fig.33 and data not shown). Phosphotyrosine levels were used to assess the activation status of each receptor (Fig. (Fig.3).3). Erbb1 appeared to have slightly increased phosphotyrosine content in the transgenic epidermis. Erbb2, and Erbb3 were active at similar levels in both the transgenic and non-transgenic epidermis. Erbb4 is not normally expressed at significant levels in the postnatal interfollicular epidermis but is expressed throughout the K14-Nrg3 transgenic skin (Fig. (Fig.3).3). We observed increased levels of Erbb4 and tyrosine phosphorylation of Erbb4 in the transgenic epidermis when compared to non-transgenic littermates. This is consistent with previous reports that Erbb4 homodimers are the major receptor for Nrg3 [61]. It is likely that cellular mechanisms exist to prevent autocrine signaling of Nrg3-Erbb4, which can be overcome in the K14-Nrg3 transgenic model. Our findings suggest that increased Erbb4 signaling in the K14-Nrg3 transgenic skin underlies the striking epidermal phenotypes observed in this transgenic model.

Erbb2 is the preferred heterodimerization partner for all of the Erbb receptors [62], so it is likely that Nrg3 elicits its effects through both Erbb2-Erbb4 heterodimers and Erbb4-Erbb4 homodimers (Fig. (Fig.3).3). Normal mammary ductal outgrowth occurs, but lactation fails in mammary glands from both heart-rescued Erbb4-null mice (where a myocardial promoter restores Erbb4 expression to the heart and overcomes embryonic lethality) and from mice in which Erbb4 has been conditionally deleted from the mammary gland [3,4]. Lobular-alveolar units from mice lacking Erbb4 in the mammary gland do not express markers of terminal differentiation and exhibit deficient proliferation of the mammary epithelium during pregnancy and at partuition. Erbb4 signaling appears to be required for secretory maturation of the alveoli since milk genes are expressed albeit at reduced levels [3]. Mammary glands from heart-rescued Erbb2-null mice display mammary ductal outgrowth defects [7,8]. Nrg1 signaling through Erbb2-Erbb4 heterodimers is required to elicit Stat5 activation and neither Erbb2 nor Erbb4 homodimers alone can activate Stat5 in vitro [63]. These results suggest that signaling through Erbb2-Erbb4 heterodimers is likely to be required to achieve terminal differentiation of the mammary gland, but not for ductal outgrowth. Nrg1-null, Erbb2-null, and Erbb4-null mice all display myocardial trabeculation defects which indicates that Nrg1 signaling through Erbb2- Erbb4 heterodimers is necessary for heart development [64-66]. Distinct neural defects including mis-innervation of the hindbrain are found in Erbb4-null mice and not in Erbb2-null mice, which suggests that this signaling occurs without utilizing Erbb2-Erbb4 heterodimers [64,65]. Erbb4 signaling regulates many other developmental pathways including the migration and differentiation of neuroblasts in the rostral-nasal stream, inhibiting cortical astrogenesis, hypothalamus-mediated reproductive development and function, and blastocyst implantation [67-71]. Signaling through Erbb4 is generally associated with cellular differentiation, particularly in the mammary gland [72]. Erbb4 signaling is likely to be far more complex since active membrane-bound, nuclear and cytosolic forms of Erbb4 exist and have been associated with other cellular processes, including apoptosis and transcriptional repression [73]. Erbb2-Erbb4 heterodimers have higher affinity than Erbb4 homodimers [74]. Signaling through Erbb heterodimers is thought to result in more potent mitogenic response than signalling through Erbb homodimers [75]. Erbb2 can bind to more phosphotyrosine binding proteins, and signaling through Erbb2-Erbb4 heterodimers is generally thought to result in more diverse and distinct outputs than signaling through Erbb4 homodimers [75,76].

We observed unusual Erbb4 JM variant profiles in the transgenic epidermis that are distinct from those observed in non-transgenic littermates. Two recent studies have shown that both the CYT-1 isoform and JM-a isoform are overexpressed in the dorsolateral frontal cortex of schizophrenic patients and suggest that dysregulated splice variant expression of Erbb4 may underlie the genetic association of Erbb4 with schizophrenia [77,78]. The four different isoforms of Erbb4 have different signaling capabilities and may mediate distinct biological functions [42,43,79]. The contribution of dysregulation of splice-variant specific expression of Erbb4 in the K14-Nrg3 transgenic skin to the phenotype we observe remains to be elucidated.

The postnatal K14-Nrg3 hyperplastic epidermal phenotypes are likely to result from induction of signaling pathways that are not normally continuously activated. Since both c-Myc and CyclinD1 are downstream target genes of β-catenin/Lef [80,81] and the Wnt pathway has well-established roles in both epithelial proliferation [82], cell fate [83], and stem cell maintenance [84], we examined Wnt/β-catenin expression in the K14-Nrg3 epidermis. However, we did not detect nuclear β-catenin, altered membranous β-catenin or E-cadherin stain or changes in Lef1 expression in the transgenic epidermis (data not shown).

K14-Nrg3 epidermis displays features indicative of perturbed basement membrane organization, including reductions in α6-integrin and β1-integrin expression levels ((9).9). α6-integrin and β1-integrin are cell surface molecules that mediate cell attachment and keratinocyte migration. Both are highly expressed in stem cells and likely to have roles in stem cell maintenance [85,86]. Both human and mouse epidermal stem cells are more adhesive to the extracellular matrix than their daughter cells [86,87]. Reduced β1-integrin levels in human keratinocytes stimulates exit from the stem cell compartment [88]. β1-integrin is required for basement membrane remodelling and for downgrowth of hair follicles [89,90]. Transgenic expression of Nrg3 within the basal epidermis also induces Tenascin-C, an adhesion-modulating extracellular matrix glycoprotein, which is often found at the sites of epithelial-mesenchymal interactions during development and tissue remodeling (Fig. (Fig.9)9) [91,92]. These results suggest that Nrg3 signaling elicits adhesive and extracellular matrix changes that are likely to have significant consequences on progenitor cell behaviour and morphogenetic events.

A number of studies have demonstrated that transgenic expression of c-Myc in the basal cells of the epidermis promotes the differentiation of epidermal stem cells into sebaceous glands. This is a strikingly similar phenotype to our observations in the K14-Nrg3 postnatal epidermis [52,53,93]. Consistent with this similarity, c-Myc expression is increased in the basal layer of K14-Nrg3 skin (Fig. (Fig.8)8) and changes in K14-Nrg3 epidermis such as hyperproliferation and increase in cell size (Fig. (Fig.2)2) are consistent with the increased basal expression of c-Myc [94-98]. The extension of expression of p63 into a large number of suprabasal cells in K14-Nrg3 skin (Fig. (Fig.9)9) suggests that Nrg3 might cause epidermal cells to exit the stem cell compartment and stimulate the proliferation of transit-amplifying cells, as is also observed in K14-c-Myc transgenic skin [53]. Also consistent with c-Myc activation is the decreased α6-integrin and β1-integrin expression observed throughout most of the basal epidermis [52,93]. c-Myc-induced repression of adhesion is thought to stimulate epidermal stem cell differentiation [93]. Our data implies that Nrg3 can alter the proliferation status of basal epidermal cells, most likely, through the induction of c-Myc. However, there are important distinctions between the K14-Nrg3 and K14-c-Myc models. K14-c-Myc mice do form hair which is gradually lost and other epithelial appendage phenotypes have not been reported [52].

These results confirm our previous studies that Nrg3 signaling can regulate epithelial cell fate during mammary gland morphogenesis and suggest Nrg3 can also regulate other pluripotent cell populations in the epidermis. Of particular interest is the ability of Nrg3 to decrease α6-integrin and β1-integrin expression, as this could be the mechanism by which Nrg3 normally elicits epithelial stratification and mammary differentiation at unique sites along the body axes during early mammary morphogenesis. Alterations in basement membrane components are known to have profound effects on progenitor populations perhaps by disrupting the stem cell niche [93,99-101]. The niche is also significantly altered in transgenic MMTV-c-Myc mammary epithelia, which show similar changes in stem cell retention and transit-amplifying cell fate decisions as observed in the K14-c-Myc epidermis [102]. Conditional deletion of c-Myc in the epidermis leads to precocious differentiation and loss of the basal progenitor cells through insufficient expansion [103]. Interestingly, another regulator of Erbb signaling, Lrig, an Egfr antagonist, acts to maintain stem cell quiescence in part by negatively regulating the c-Myc promoter [104]. Conditional deletion of Rac1, a negative regulator of c-Myc leads to rapid depletion of the stem cell compartment and highlights their critical roles in stem cell regulation [105].

We propose that when Nrg3 is ectopically expressed in to the postnatal period, as in the K14-Nrg3 model, the transit-amplifying cells may differentiate to form the interfollicular epidermis and sebaceous lineages by effectively the same means as proposed by Arnold and Watt [53] and Frye et al. [53,93] for the role of c-Myc in the epidermis. In this model, sustained c-Myc activation promotes sebaceous formation at the expense of the hair lineage; sustained Nrg3 expression appears to elicit the same effect. c-Myc expressing human keratinocytes exhibit decreased cell motility [93] which could explain the failure of the hair lineage differentiation in both the K14-c-Myc and K14-Nrg3 models. Keratinocytes must migrate out from the bulge down to receive the hair inductive signal from the dermal papilla [106,107]. It appears that the sebaceous lineage is conferred on keratinocytes that fail to migrate to the dermal papilla and remain in the bulge.

The exact mechanism by which mammalian epithelia stratifies is not known but p63 is central to this process as stratification fails in its absence [56,108,109]. Recently p63 has been implicated as a key regulator of cellular adhesion and survival of basal cells in the mammary gland and other stratified epithelia [110]. Two models have been proposed (citing either delamination [111,112] or asymmetric cell division [113,114]) for how the stratification of epithelia is elicited. To what degree these contribute to epithelial morphogenesis remains to be ascertained. The onset of stratification during embryogenesis is thought to be elicited by asymmetric cell division [113,114]. Mammary placodes are thought to arise as a result of local cell migration [30] but, initial stages are characterized by stratification [31,32], which is thought to be elicited by basal cell proliferation.

Changes in the adhesive properties of epithelial cells have been described as a general phenomena during the very early stages of bud formation of other organs including the hair follicle, submandibular gland, and mammary gland [115-118]. Both desmosomal and hemidesmosomal expression profiles are downregulated during early mammary bud formation and thought to mediate differences in cell adhesive properties within the forming bud which are subsequently restored during later stages of mammary gland formation [117]. It has been hypothesized that epithelial cells that form the hair follicle respond to the inductive signals from the dermal mesenchyme by changing their cell adhesion properties and that this mediates early morphogenesis [116]. Whether similar changes in adhesive processes are relevant to the very early stages of mammary development (i.e. the initial stratification and placode formation) remain to be determined. The expression of Nrg3 in the dermal mesenchyme at the sites where mammary placodes will form prior to their morphological appearance and the ability of Nrg3 to elicit placode formation in explanted embryo cultures would suggest Nrg3 could mediate changes in the adhesive components of the epithelium that lead to formation of the mammary placode.

Conclusion

Nrg3 is a key regulator of mammary fate. Ectopic expression of Nrg3 induces the formation of supernumerary mammary glands, the expression of c-Myc, and promotes sebaceous gland fate rather than along the hair follicle lineage. Deregulated Nrg3 expression in stem cells reduces the expression of α6-integrin and β1-integrin, both of which are essential for stem cell maintenance and keratinocyte migration. Nrg3 may have roles in promoting mammary lineage commitment and regulation of stem cell maintenance via c-Myc. Further studies of Nrg3 are warranted to discern how mammary epithelial stratification is elicited, particularly with regard to how it coordinates interactions with other signaling pathways and to what degree basal epithelial proliferation contributes to this process.

Methods

Generation of K14-Nrg3 mice

The cDNA for mouse Nrg3 was excised and cloned into the ClaI and SpeI sites of K14-β-globin and an SV40 polyadenylation site was added. The transgene was released from the vector with KpnI and microinjected into fertilized B6 × CBA F1 eggs. Transgenic mice were identified by Southern blotting of tail DNA using a Nrg3 cDNA probe.

Histology, Immunohistochemistry and Immunoflourescence

Skin samples were fixed overnight in 4% paraformaldehyde, formalin, or Carnoy's and then paraffin embedded or embedded in OCT and then frozen immediately in an isopentane bath. Sections (5 μm) were rehydrated, processed with microwave or pressure cooker antigen retrieval if required, and blocked and were incubated with primary antibodies overnight at room temperature.

For immunohistochemistry, peroxidase-labeled polymer (Envision rabbit, Dako, Glostrup, Denmark) was used for detection of primary antibodies raised in rabbits. Biotin-labeled donkey anti-goat IgG antibody (Molecular Probes, Eugene, OR, USA) was used for detection of the goat antibodies using Vector ABC kit (Vector Labs, Burlingame, CA, USA) or Goat Histofine Simple Stain MAX PO (Nicherei, Chou-ku, Tokyo, Japan). Rat Histofine Simple Stain Mouse MAX PO (Nicherei) was used for detection of the rat antibodies. Biotin-labeled rabbit anti-sheep IgG antibody (Vector Labs) was used for detection of the sheep antibodies. MOM kit (Vector Labs) was used for detection of mouse monoclonal antibodies. 3,3' diaminobenzidine was used as chromagen and sections were counterstained with hematoxylin.

The primary antibodies, dilutions, and antigen retrieval conditions used for immunohistochemistry are listed in Additional File 6.

For immunoflourescence, alpha6 integrin antibody (BD Pharmingen) was used on frozen sections at 1:5 dilution followed by secondary anti-rat (Invitrogen, Molecular Probes) antibody conjugated to Alexa Fluor 488 fluorochrome. Nuclei were labeled by using 4'6'-diamidino-2-phenylindole (DAPI). Sections were mounted in Vectashield. Fluorescence samples were examined at room temperature using a TCS SP2 Leica microscope with an Acousto-Optical Beam Splitter.

Oil Red O staining was performed using the standard protocol [119]. Whole mount in situ hybridization was performed with Nrg3 probe as previously described [2].

Western blots

Skin samples were homogenized with a Polytron in modified RIPA buffer (50 mM Tris-HCl pH 7.4, 1% Triton X-100, 0.2% sodium deoxycholate, 0.2% SDS, 1 mM EDTA) with protease inhibitors (1 mM PMSF, 5 μg/ml aprotinin, 5 μg/ml leupeptin, 1 mM NaF, 1 mM orthovanadate, 1 mM DTT). Homogenates were analyzed on 10% polyacrylamide gels and transferred to Hybond C extra membranes (GE Healthcare). Filters were incubated with anti-c-Myc (Upstate) overnight at 4°C, washed and incubated with peroxidase-conjugated anti-rabbit IgG (GE Healthcare) and visualized with enhanced chemiluminescence detection kit (ECL, GE Healthcare).

Immunoprecipitation

Erbb receptor phosphorylation was detected by immunoprecipitating lysates from skin samples with individual receptors and immunoblotting as described [120].

RT-PCR

Erbb4 isoform levels were determined by semiquantitative RT-PCR. cDNAs from transgenic and non-transgenic skin samples were analyzed for Erbb4 mRNA variants. A 1.0-μL portion of each cDNA was used as a template in PCR containing 0.3 μM of each primer, 2.25 mM MgCl₂, 0.5 mM of each dNTP, and 2.5 U of Expand long template enzyme mix (Roche). The amplification conditions were 92°C for 2 min, followed by 35 cycles of 10 sec at 92°C, 30 sec at 57°C (for JM) or 63°C (for CYT), 3 min at 68°C, and a final step of 7 min at 68°C. The following primers were used to amplify the CYT variant of the Erbb4 coding region: Erbb4CYTF, GCTGAGGAATATTTGGTCCCCCAG; Erbb4CYTR, AAACATCTCAGCCGTTGCACCCTG. The following primers were used to amplify the JM variant of the Erbb4 coding region: Erbb4JMF, GAAATGTCCAGATGGCCTACAGGG; Erbb4JMR, CTTTTTGATGCTCTTTCTTCTGAC. Specificity was verified by sequencing. As a control, Gapdh was amplified in parallel. Gapdh levels were also determined by semiquantitative RT-PCR.

Abbreviations

Egfr, EGF receptor; HRG, Heregulin; K14, Keratin14; Nrg3, Neuregulin3.

Competing interests

The author(s) declares that there are no competing interests.

Authors' contributions

HP collected tissues, carried out immunohistochemistry, molecular and morphological analysis. OS and SP carried out tissue sectioning and immunohistochemistry. AA participated in the design of the study and helped draft the manuscript. BH conceived and coordinated the study, assisted with experiments, and wrote the manuscript. Figures were prepared by HP and BH. All authors read and approved the final manuscript.

Supplementary Material

Additional file 1

Shows Nrg3 and Erbb4 expression in the hair follicles.

Click here for file^{(245K, pdf)}

Additional file 2

Shows results from PCR genotyping of founder generation of K14-Nrg3 transgenic mice.

Click here for file^{(55K, pdf)}

Additional file 3

Shows the efficiency of transgenesis for males versus females.

Click here for file^{(37K, pdf)}

Additional file 4

Shows the phenotype of a chimeric K14-Nrg3 founder mouse.

Click here for file^{(193K, pdf)}

Additional file 5

Shows results of analysis of transgenic skin using immunohistochemistry of epidermal differentiation markers.

Click here for file^{(322K, pdf)}

Additional file 6

Is a list of antigen retrieval methods used for the immunohistochemistry.

Click here for file^{(53K, pdf)}

Acknowledgements

This work was funded by Breakthrough Breast Cancer. We thank Vladimir Grigoriev for generation of transgenic mice, staff of the ICR BSU for animal care, Jorge Reis-Filho for help with pathological analysis, Michelle James, Kay Savage, and Dawn Steele for excellent assistance with histopathology, Dave Robertson for assistance with confocal microscopy, and Carrie Ambler for helpful suggestions.

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HArDcore RuLes :):)HtId ALl da MOther Fuckin wAY: .*:•.[..WeLcOmE..].• . • .*:•.[ T o ].• .• . *:•....[..The..].• .•: *:•.*:.[ World Of ].• :•.[..1o0% pUrE..].•* :•.[ H A R D C O R E!]: HTId HArdcore tiLL i FUckiN DIe, CArry On stoMPin RAvers iM a SToMPaHOlic A RAVeaHOlic and A HArdcoholic

H-A-R-D-C-O-R-E <<<<<
BELOW IS ALL THE RAVES FROM BK IN DA DAY EVO BEST CLUB EVER,

2010-04-12T03:51:00.000-07:00

Hello people im pete as u can see im a mad raver lol,i love raves,its all about the Music the lasers and the flashy lights n oh yea the drugs lol,my favourite dj's are HIXXY cos hes da best hes old school,scott brown an absolute legend,u couldnt get them any more crazier than cally juice,lisa lashes,lisa pinup,tidyboys,showtek,alex kid and Joeyyyyyyyyy riot,darren styles is awesome as well that song i cant get u out of my head and flashlight and say u love me again all banging tunes,i live for my hardcore,listening to an old song of hixxys now called night life n then gonna listen to overload :):)i have loads of tatoos haha funny enough to show im dedicated to my hardcore music i have HTID tatooed on me wrist =hardcore till i die woop woop mental aint i haha,i hope u like my blogs i cud write a book about my life haha so much has happened n all,my youtube page is www.youtube.com/ultimateraver23 if u wanna leave any comments or if u need help with anything i will be happy to assist you,its all about the hardcore ravers,im a raver i reach the sky im hardcore till i die as u touch me i feel ur heart beating next to mine i want u forever n ever,This is me n all me Muccas,Markie boi,stevie,Georgie
Timmo,Jody,Mart,

2010-04-12T02:40:00.000-07:00

THis is mdai its a cross between Mdma and cocaine its very nice stuff with a very nice relaxed and calm buzz,no comedown watsoever now does dis seem like the new safer mephedrone we will see,im injesting about 120mg now n i will let u know what it feels like,dis is a new product,it doesnt bother me mephedrone is banned ive had my time on it n it was nice while it lasted,but i love trying new products 2 see if the effects are stronger than real drugs like mdma and cocaine,im sitting here listening to my hardcore music adam harris its over now,bangin tune and hes a wicked Dj starting to feel a little bit of eye twitchiness feeling a bit nice now,feel a bit of a tingle goin through me hmmm,ive just recorded a video and its on my site now,will show u what u can expect from this new product MDAI in my opinion its nicer than mephedrone,doesnt give u a comedown doesnt mess ur head up,doesnt make u paronoid just fink of euphoria but a completly clear head not 2 intense and not lethal :):)im feeling so good it feels like real mdma

MDAI the New drug thats gonna be the nicest thing since MDMA

2010-04-11T18:47:00.000-07:00

Four cyclic analogues of the psychoactive phenethylamine derivative 3,4-(methylenedioxy)amphetamine were studied. These congeners, 5,6- and 4,5-(methylenedioxy)-2-aminoindan (3a and 4a, respectively), and 6,7- and 5,6-(methylenedioxy)-2-aminotetralin (3b and 4b, respectively) were tested for stimulus generalization in the two-lever drug-discrimination paradigm. Two groups of rats were trained to discriminate either LSD tartrate (0.08 mg/kg) from saline, or (+/-)-MDMA.HCl (1.75 mg/kg) from saline. In addition, a 2-aminoindan (5a) and 2-aminotetralin (5b) congener of the hallucinogenic amphetamine 1-(2,5-dimethoxy-4- methylphenyl)-2-aminopropane (DOM) were also evaluated. None of the methylenedioxy compounds substituted in LSD-trained rats, while both 3a and 3b fully substituted in MDMA-trained rats. Compounds 4a and 4b did not substitute in MDMA-trained rats. Compounds 5a and 5b did not substitute in MDMA-trained rats, although 5a substituted in LSD-trained rats, but with relatively low potency compared to its open-chain counterpart. In view of the now well-established serotonin neurotoxicity of 3,4-(methylenedioxy)amphetamine and its N-methyl homologue 1, 3a and 3b were evaluated and compared to 1 for similar toxic effects following a single acute dose of 40 mg/kg sc. Sacrifice at 1 week showed that neither 3a nor 3b depressed rat cortical or hippocampal 5-HT or 5-HIAA levels nor were the number of binding sites (Bmax) depressed for [3H]paroxetine. By contrast, and in agreement with other reports, 1 significantly depressed all three indices of neurotoxicity. These results indicate that 3a and 3b have acute behavioral pharmacology similar to 1 but that they lack similar serotonin neurotoxicity.

I have had the opportunity to try MDAI and done so twice and in a party setting each time. Clearly empathogenic, although the first time I took a while to realise it. Gives this slight I'm-in-a-bubble kind of feeling, and pupils fairly dilated, makes for a smooth and comfy evening.

What it didn't do however was make me disoriented and dizzy like MDMA, nor as crazily euphoric as M1.

Both times I combined with cannabis and alcohol. And I think the second time it may have been followed by a moderate dose of butylone, with which it also combined well.

Only moderate serotonin burnout, I feel.

Definitely a lot less than MDMA, and also less than mephedrone (4-methyl-meth-cath) and WAY less than 4-methpxy-meth-cath.

A mild AMT-style vibe to it in how it creates this "comfortable comfort-cloak" but with none of the psychedelia.... just pleasant, would do again if I had the possibility.

Dosage similar to MDMA, perhaps a tad higher, up to 200mg...

ABOUT NRG 1 very dangerous and evil

2010-04-11T18:45:00.001-07:00

GUYS I THOUGHT THIS DRUG WAS GONNA BE AMAZING WAS REALLY EXCITED ABOUT IT,I GONNA BE BUYING A GRAM OF EACH OF THE NEW ONES DAT AVE COME OUT NOW N I WILL KEEP U POSTED COS WHEN CHINA FOUND OUT THAT THE UK WAS GONNA BAN MEPHEDRONE THEY MADE 6 PRODUCTS TO TAKE OVER MEPHEDRONE,SUM CUD BE MORE DANGEROUS SUM CUD BE REALLY GOOD WE JUST GONNA AVE TO WAIT N SEE, I WILL DO RESEARCH INTO EM N LET U KNO ABOUT THE EFFECTS N HOW LONG IT TAKES U TO COME UP EXE,, IM GLAD I FLUSHED IT DOWN THE TOILET,CHINA HAS REALLY GONE 2 FAR THIS TIME,MEPHEDRONE IS NOTHING COMPARED 2 DIS,DIS NRG 1 IS MORE STRONGER THAN MDMA COCAINE N MORE EDDICTIVE THAN HEROIN,THEY SHOULDNT OF BANNED MEPHEDRONE COS NOW THEY GOT THIS DANGEROUS DRUG THATS MORE HARMFUL,WILL KILL MORE PEOPLE IF SOMETHING AINT DONE ABOUT IT,LEGALISE MDMA THEN NO MORE PROBLEMS,IF A SMALL TINY LINE CAN FUCK U UP WID ALL THOSE SIDE EFFECTS THEN WAT WILL A BIG LINE DO? COS EVERYONE WUD DO BIG LINES OF DRONE NOT GIVIN A DAMN ABOUT WHAT ITS GONNA DO N THEN IT MESSED US UP,U CAN OVERDOSE OFF 0.1 OF A GRAM OF DIS RUBBISH ITS MESSED UP,

MY EXPERIENCE ON NRG 1 DONT MESS WID IT IT WILL MESS WID U

2010-04-11T18:34:00.000-07:00

people i never ever experienced a problem with mephedrone it isnt the mephedrone every mephedrone batch is diffrent,every batch ive ever bought on the net i have had a taster,sum of the batches i bought Tasted Like cocaine numbed me mouth i loved dat feeling i never had a problem with those batches,where another tasted like very nasty near enough poisonous chemicals n another wud taste like nothing just Horrible Sea salt rank as fuck,those batches are da dodgy ones,the ones where u got the coke taste is proper mephedrone they shouldnt blame the name cos it aint its what ppl put in with it like,ive never had no health problems off mephedrone and i used 2 cane it cos the mdma situation was so crap n pills werent worth getting,i USed 2 do fat lines n all sorts,But i been in da drug scene for ten years so any new drug i make sure i get as much info n videos on it as i can b4 i take the substance,me m8 told me about dis new drug dat had come out he gave me the link,by looking at dis u wud fink exacly the same as i did,oooo amazing omg it seems so wicked seems like its gonna be the closest safest thing to mdma n says its stronger than coke 2 ooooo i cant wait for dis,sod mephedrone if it gets banned lets try dis one out n see if its any diffrent, heres the facts about it,i couldnt belive it i fort finally we mite get a new drug dat wont kill many ppl like drone did,notice the name RAVE, if i hadnt of tested dis out before goin on a nite out just in da day 2 see wat it wud do 2 me i wud proberly be dead,It is the most dangerous drug ive ever tryed,n i been doin drugs for ten years legals n class a's n never have had much health worries wid any drug,So me n my girl open the bag it says HAzard n harmful on the sticker nothing about not for human consumption,n dis was after i had seen it on da news but i didnt wanna belive it i fort the guy was talkin rubbish n fort i will find out for myself,it cant be dat bad why wud china bring out sommin that wud kill thousands n not even ave a good time on it,unless they wanna wipe out the uk dat is,which dis drug is already is in playgrounds,one kid cryed all the water out of his body and was sick,apparently if ur sick on dis it will kill u,i Tasted it orally just a fingernail full,very rank very sour very chemically n tasted poisionous,i fort nothing of it n i Made a tiny small line for me n my girl really small, like match stick size,we snorted it,the feeling felt great wen it went up our noses,it felt like i was on cocaine,n then it kicked in,we couldnt stop smiling all happy n all,i banged on sum music,everything was goin great n then 30 mins or so l8er,i Started to lose my focus we couldnt focus on the tele or anything,we kept finkin were being paronoid it will go away,we waited a bit n it didnt,n then we couldnt talk to eachother,the room was spinning,finding it hard to put a simple convo 2gether,i felt dizzy,headache,like i was burning,me throat was killing me nose hurt,but it gets worse,we suddenly started tripping seein 3 or everything and sweating loads,we drank so much water and squash it was unreal,we didnt want to get close 2 eachother we both couldnt talk,we just looked at eachother,n Then we started aching,we went for a walk it was like evryone was lookin at us we couldnt put our head up,8oclock now still on dat rubbish,worse than ever,depression kicks in,paronoid thoughts,we felt like we was in hell,i was goin on about my past n gettin into a state worryin n all,we didnt sleep all nite,we only did a very minute line n it messed us up until 11 am 2day,im so glad its out of my system now,ive neveer felt so frightened in all my life this is gonna kill thousands of people,and if an experienced user like myself does a tiny line n im used 2 doin loads of lines if i had done a big line i wud be in hospital now or even dead cos i wud of drank booze as well,even drone was 99.88% pure but as i sed it never scared me drone is baby meow dis is like the big momma,think ten times worse than cocaine n more addictive than heroin, i flushed it down the toilet 2day good riddance to the devils powder,im still in shock from it,im glad i did dat 2 risky i cud of taken it again n it cud of killed me,cos its so pure u can overdose over a 0.1 line its messed up stuff,n it messed up my gf as well who doesnt touch stuff Now wat is it gonna do 2 kids,ppl will be doin loads of lines of dis n it wil kill you,dont mess wid dis dangerous substance i hope it gets banned b4 ppl start dropping like flies im glad we didnt do anymore cos it cud of killed us,they need to legalise MDMA dis is gonna kill more ppl than the plague,its already shipping from china in thousands of kiligrams,its on our streets,only a matter of time wen theres a death,

NRG-1 is a 25p hit and will kill many more than meow
From VIRGINIA WHEELER
in Antwerp, Belgium

A BRIT chemist who helped flood the UK with meow meow has warned of an even DEADLIER legal high about to hit us.

Worried Dave Llewellyn told The Sun that the new drug NRG-1 will be "Britain's worst nightmare" leading to mass brain damage and death.

The horror drug COSTS just 25p a hit compared to £10 for a rock of crack cocaine, yet it is 13 times STRONGER than coke and even more ADDICTIVE than heroin.

But authorities are powerless to prevent it flooding our streets because it is completely LEGAL.

Dave, a drug manufacturer and legal stimulant seller based in Belgium, said yesterday: "It is the worst drug ever to hit the shores of Britain. It makes meow meow look like baby powder.

"It will wreck hundreds of lives and kill many times more than meow meow - and far more horrifically. It will make users want to tear out their own eyes.

"It makes people feel like God Himself - but really it is the Devil's Powder."

Scots-born Dave admits sending meow meow to Britain but has stopped after it was implicated in 26 deaths. He agreed to speak to The Sun amid moves to make the substance, officially known as mephedrone, illegal in Britain.

He turned whistleblower to us in a bid to prevent NRG-1 - which also has the street names Energy 1 or Rave - reaching the UK's markets too.

He said the new drug, otherwise known as naphyrone, would kill and mentally destroy so many people it would quickly "fill an Olympic stadium".

Speaking to us in the port city of Antwerp, he warned: "Naphyrone comes from Chinese factories and what it does to users is truly frightening.

"It will make them feel like God for about 12 hours. But when it wears off they will feel worse than they ever have in their lives. They won't sleep for three days.

"It juices the brain, causing cerebral burn-out of a degree not seen before. It causes paranoia and suicidal tendencies and permanently alters brain chemistry with horrifying consequences."

And he went on: "The worst thing is that it is completely legal. It is being marketed as a mephedrone replacement and will be bought by children.

"It can be made by anyone with a GCSE in chemistry for around 10p a gram. That would give one person around 80 hours of the ultimate legal high, then destroy them.

"Such a tiny amount is needed that it will turn up in playgrounds for 25p a hit. I think it will become Europe's crystal meth."

Dave said each hit of naphyrone was 13 times more potent than cocaine. And just a few granules of the off-white powder have the chemical effect of a "mega speedball" - like taking crystal meth, cocaine and ecstasy combined.

Dave added: "I won't sell meow meow again because of what has happened in Britain, with people selling the drug and then not telling them it can become lethal when mixed with alcohol.

"Marketing it as plant food is the most idiotic thing that could ever happened. That decision cost lives.

"But naphyrone is the one that sends shivers down my spine. I won't touch it and want to warn people how terrifying this drug is."

Dave, who left the UK to run Alchemy Labz selling "ethical" stimulants on the Continent, showed us dozens of websites already flogging naphyrone to Brits.

And drugs forums are crammed with questions from excited youngsters about the "brand new" meow meow - at the same time as seasoned users warned against it.

One posted: "It is flying to Heaven - and waking up in Hell."

The chemical make-up of both mephedrone and naphyrone are only slightly different - and BOTH are terrifyingly similar to ecstasy.

Dave explained that mephedrone gives users a high by overdosing the body's pleasure receptors.

But naphyrone works by over-stimulating not only those receptors, but also ones which flood the body with adrenaline. The combination causes brain "fry-out".

Dave has written to Home Secretary Alan Johnson and the Drugs Advisory Council about his fears.

He insisted: "No drug is safe and I am definitely not advertising meow meow now. If I ever thought there was a one per cent chance someone would die from a drug I would not sell it at all.

"I understand the chemistry and I want to do the right thing. There needs to be serious action taken, driven by facts and not hysteria.

"There needs to be an open discussion and it needs to hear from law enforcement officers, politicians, youth workers, scientists - and also drug users."

UK drug websites were buzzing with talk about the new substance last night. One user who had tried it warned: "Can't sleep, very bad comedown. Sweating all night."

Dave said: "I am stopping the sale of mephedrone in the UK due to the new legal position.

"I find it terrible that, under the Medicines Act, people have to sell it as plant food - which makes it illegal to tell people that it can be lethal if mixed with alcohol and in fact should not be mixed with any other substance.

"Criminalising people for giving out safety information on what everyone knows is a drug is the most idiotic thing that could ever have happened."

He also explained that there are three different strengths of NRG1 (naphyrone.)

And he added: "Naphyrone is NOT the same as mephedrone in its effects. It is not a replacement. It is a killer."

Link: http://www.thesun.co.uk/sol/homepage...than-meow.html

WHY PPL STARTED TAKING MEPHEDRONE

2010-04-11T18:05:00.000-07:00

As you can See all these batches are diffrent,check the change of colour and all,mephedrone is never the same,
its always diffrent,u can get good batches and u can get really bad ones,lucky for me ive had more good batches than bad ones,People started taking mephedrone when it spread across the net that a drug was coming out that was legal n u cud buy really cheap off the net n be delivered next day,This was mephedrone,i had no idea what this was,it was my mate that helped me out,he told me he was getting sum n for me to try it with him one nite,it came in a tightly sealed envelope in a small bag,when we looked at it we couldnt belive it,millions of little crystals,So we decided to have a couple of lines,i fiink we did about 5 to get us started but cos we both was so used 2 drugs anyways we wasnt scared about ttrying sommin new,We started feeling a bit of a buzz after about an hour,we starteed feeling like we had just done a line of pure cocaine which u cant get these days all drugs have gone down hill,the buzz felt amazing,we put on sum dance music and it felt like mdma we just felt close to eachother n we couldlnt stop smiling,we then decided we wanted to go clubbing so we went clubbing and it was amazing we took a bit more n then didnt fink it was hitting us so we had more,we didnt realise how addictive this stuff was,It got to the stage where it wore off and we hated it,we felt paronoid and also a little bit aggressive thinking people were looking at us when they wasnt,it was because we was so used 2 other drugs like pills or mdma we didnt fink it wud put us in a gurning mess,i have been doing my research on mephedrone for 2 years,read up about it done videos on youtube as u can see to warn people of the dangers of this new dance drug,in my experience it is a nice drug but if u overdo it u will lose the enjoyment and will just get depressed and paronoid,i dont do much of it dat much but its nice 2 ave a little line ere n there like,but i dont reccomend u take it if u havnt got a clue what is it,its a pure drug,as the batches show it can be diffrent each time u get it,u cud get a batch dat cud kill you,dis is not a toy it is a research chemical that not much research was done on it when it shud of been,now we had all those people dying,one cos they didnt kno what the drug wud do,2 they fort it was legal yea i assume thats safe,and 3 They werent really into drugs n didnt kno much about them,those 3 things there is why it effected them,when ur trying sommin new make sure u do as much research and resiting the drug as u can b4 u consume,with me i consume alot of research chemicals,i list my results in my videos,wat the side effects are,how i felt exe exe,If you do this in moderation its ok but dont overdo it,make sure when u first try it that ur with friends and not on ur own and it shud not be bannned it shud be labeled as 18+ if u gonna ban mephedrone why dont you make mdma legal again n then the price shud go down n ppl wont die,hardly anyone has died from ecstasy but drone is a diffrent kettle of fish it is a dangerous evil drug if not used properly,just u got to kno what ur doing,

2010-04-11T17:41:00.000-07:00

THis is Mephedrone also known as meow aka m-cat,it looks nice doesnt it but what u dont understand is when you snort the first line u mite want more and more and u will become dependent,mephedrone is very addictive i have been doing it for two years,the first time i tryed it was cos the situation for mdma was so bad,all ecstasy pills dat were meant to have mdma in,no longer did,they had sommin worse called BZP,piperazine which used 2 be in those pep pills bk in the day,i remember them they were good but they did fuck alot of ppl up,MDMA is da best,but now the Goverment is thinking of banning mephedrone,very stupid idea,because by them doing this is gonna cause a big problem as mephedrone will go underground it wont be the m-cat we kno n love,it will be
cut with all sorts of crap rangin from rat poison to toilet
cleaner n so on,there are a load of substances that are being shipped over as we speak,we will ave 2 2 wait and see what these have in store for us store the closest thing to mdma or cud they b more lethal