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[h=1]Androgen actions on the human hair follicle: perspectives.[/h]Inui S, Itami S.
[h=3]Source[/h]Department of Regenerative Dermatology, Graduate School of Medicine, Osaka University, Osaka, Japan. inui@r-derma.med.osaka-u.ac.jp
[h=3]Abstract[/h]Androgens stimulate beard growth but suppress hair growth in androgenetic alopecia (Androgenetic Alopecia). This condition is known as 'androgen paradox'. Human pilosebaceous units possess enough enzymes to form the active androgens testosterone and dihydrotestosterone. In hair follicles, 5α-reductase type 1 and 2, androgen receptors (AR) and AR coactivators can regulate androgen sensitivity of dermal papillae (DP). To regulate hair growth, androgens stimulate production of IGF-1 as positive mediators from beard DP cells and of TGF-β1, TGF-β2, dickkopf1 and IL-6 as negative mediators from balding DP cells. In addition, androgens enhance inducible nitric oxide synthase from occipital DP cells and stem cell factor for positive regulation of hair growth in beard and negative regulation of balding DP cells. Moreover, Androgenetic Alopecia involves crosstalk between androgen and Wnt/β-catenin signalling. Finally, recent data on susceptibility genes have provided us with the impetus to investigate the molecular pathogenesis of Androgenetic Alopecia.
© 2012 John Wiley & Sons A/S.
[h=3]Source[/h]Department of Regenerative Dermatology, Graduate School of Medicine, Osaka University, Osaka, Japan. inui@r-derma.med.osaka-u.ac.jp
[h=3]Abstract[/h]Androgens stimulate beard growth but suppress hair growth in androgenetic alopecia (Androgenetic Alopecia). This condition is known as 'androgen paradox'. Human pilosebaceous units possess enough enzymes to form the active androgens testosterone and dihydrotestosterone. In hair follicles, 5α-reductase type 1 and 2, androgen receptors (AR) and AR coactivators can regulate androgen sensitivity of dermal papillae (DP). To regulate hair growth, androgens stimulate production of IGF-1 as positive mediators from beard DP cells and of TGF-β1, TGF-β2, dickkopf1 and IL-6 as negative mediators from balding DP cells. In addition, androgens enhance inducible nitric oxide synthase from occipital DP cells and stem cell factor for positive regulation of hair growth in beard and negative regulation of balding DP cells. Moreover, Androgenetic Alopecia involves crosstalk between androgen and Wnt/β-catenin signalling. Finally, recent data on susceptibility genes have provided us with the impetus to investigate the molecular pathogenesis of Androgenetic Alopecia.
© 2012 John Wiley & Sons A/S.