Va. Randall et al., Do androgens influence hair growth by altering the paracrine factors secreted by dermal papilla cells?, EUR J DERM, 11(4), 2001, pp. 315-320
Androgens regulate many aspects of human hair growth in both sexes. After p
uberty they transform tiny vellus follicles in many areas, e.g. the face, t
o terminal ones producing long, thick, pigmented hairs. In genetically pred
isposed individuals, androgens also cause the reverse transformation of ter
minal scalp follicles into vellus ones, causing balding. In the current hyp
othesis for androgen action, androgens control most follicular cells indire
ctly acting via the mesenchyme-derived dermal papilla which regulates many
aspects of follicular activity. In this model androgens binding to androgen
receptors in dermal papilla cells alter their production of regulatory mol
ecules which influence other follicular components; these molecules may be
soluble paracrine factors and/or extracellular matrix proteins.
This hypothesis is supported by immunohistochemical localisation of androge
n receptors in dermal papilla cell nuclei and the demonstrations that andro
gen receptor content and testosterone metabolism patterns of cultured derma
l papilla cells from various body sites reflect hair growth in androgen-ins
ensitivity syndromes. The next question is whether androgens alter the para
crine factors secreted by dermal papilla cells, Cultured dermal papilla cel
ls do release soluble, proteinaceous factors into their media which stimula
te the growth of keratinocytes and other dermal papilla cells. This mitogen
ic potential can cross species from humans to rodents. Importantly, testost
erone in vitro stimulates the mitogenic potential of beard cells, but in co
ntrast inhibits production by balding scalp cells reflecting their in vivo
androgenic responses.
Since androgen in vitro do alter the secretion of paracrine factors the cur
rent focus lies in identifying specific factors produced, e.g. IGF-I and st
em cell factor (SCF), using ELISA and RT-PCR, and comparing their expressio
n in cells from follicles with varying responses to androgens in vivo or un
der androgen stimulation in vitro. This should lead to greater understandin
g of androgen action and enable the development of better treatment for adr
ogen-potentiated disorders.