Interesting on immunosuppressant

waynakyo

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[h=1][FONT=Verdana, Arial, Tahoma, Calibri, Geneva, sans-serif]Mycophenolate Antagonizes IFN-γ-Induced Catagen-Like Changes via β-Catenin Activation in Human Dermal Papilla Cells and Hair Follicles.[/FONT][/h][FONT=Verdana, Arial, Tahoma, Calibri, Geneva, sans-serif]Ryu S1, Lee Y2, Hyun MY3, Choi SY4, Jeong KH5, Park YM6, Kang H7, Park KY8, Armstrong CA9, Johnson A10, Song PI11, Kim BJ12.[/FONT]
[h=3][FONT=Verdana, Arial, Tahoma, Calibri, Geneva, sans-serif]Author information[/FONT][/h]

[h=3][FONT=Verdana, Arial, Tahoma, Calibri, Geneva, sans-serif]Abstract[/FONT][/h][FONT=Verdana, Arial, Tahoma, Calibri, Geneva, sans-serif]Recently, various immunosuppressant drugs have been shown to induce hair growth in normal hair as well as in alopeciaareata and androgenic alopecia; however, the responsible mechanism has not yet been fully elucidated. In this study, we investigate the influence of mycophenolate (MPA), an immunosuppressant, on the proliferation of human dermal papilla cells (hDPCs) and on the growth of human hair follicles following catagen induction with interferon (IFN)-γ. IFN-γ was found to reduce β-catenin, an activator of hair follicle growth, and activate glycogen synthase kinase (GSK)-3β, and enhance expression of the Wnt inhibitor DKK-1 and catagen inducer transforming growth factor (TGF)-β2. IFN-γ inhibited expression of ALP and other dermal papillar cells (DPCs) markers such as Axin2, IGF-1, and FGF 7 and 10. MPA increased β-catenin in IFN-γ-treated hDPCs leading to its nuclear accumulation via inhibition of GSK3β and reduction of DKK-1. Furthermore, MPA significantly increased expression of ALP and other DPC marker genes but inhibited expression of TGF-β2. Therefore, we demonstrate for the first time that IFN-γ induces catagen-like changes in hDPCs and in hair follicles via inhibition of Wnt/β-catenin signaling, and that MPA stabilizes β-catenin by inhibiting GSK3β leading to increased β-catenin target gene and DP signature gene expression, which may, in part, counteract IFN-γ-induced catagen in hDPCs.[/FONT]

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I would be very interested in the literature backing their claim in the first sentence. Encouraging.
 

benjt

Experienced Member
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100
The literature they cite for the statements in the first sentence is:


  • 17. Iwabuchi, T.; Maruyama, T.; Sei, Y.; Adachi, K. Effects of immunosuppressive peptidyl-prolyl cis–trans isomerase (PPIase) inhibitors, cyclosporin A, FK506, ascomycin and rapamycin, on hair growth initiation in mouse: Immunosuppression is not required for new hair growth. J. Dermatol. Sci. 1995, 9, 64–69.
  • 18. Paus, R.; Bottge, J.A.; Henz, B.M.; Maurer, M. Hair growth control by immunosuppression. Arch. Dermatol. Res. 1996, 288, 408–410.
  • 19. Parodi, A.; Rebora, A. Topical cyclosporine in alopecia areata. Arch. Dermatol. 1987, 123, 165–166.
  • 20. Paus, R.; Stenn, K.S.; Link, R.E. The induction of anagen hair growth in telogen mouse skin by cyclosporine A administration. Lab. Investig. 1989, 60, 365–369.
  • 21. Pendry, A.; Alexander, P. Stimulation of hair growth on nude mice by cyclosporin A. In Cyclosporin A: Proceedings of An International Conference on Cyclosporin A; Elsevier Biomedial Press: Armsterdam, The Netherlands, 1981.
  • 22. Sainsbury, T.S.; Duncan, J.I.; Whiting, P.H.; Hewick, D.S.; Johnson, B.E.; Thomson, A.W.; Oliver, R.F. Differential effects of FK 506 and cyclosporine on hair regrowth in the DEBR model of alopecia areata. Transplant. Proc. 1991, 23, 3332–3334.
  • 23. Sawada, M.; Terada, N.; Taniguchi, H.; Tateishi, R.; Mori, Y. Cyclosporin A stimulates hair growth in nude mice. Lab. Investig. 1987, 56, 684–686.
  • 24. Yamamoto, S.; Kato, R. Hair growth-stimulating effects of cyclosporin A and FK506, potent immunosuppressants. J. Dermatol. Sci. 1994, 7, S47–S54.
 

hellouser

Senior Member
My Regimen
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Link to source??????????
 

IDW2BB

Established Member
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19
Androgens + genetic susceptibility = male pattern baldness

We can attack the androgens with castration or modifying 5AR(I&II)

Looks like we might be able to attack male pattern baldness via the immune system.

Might have to change the name from Androgenetic Alopecia to AGIA.

Genes of the immune system may come into play.
 
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