Hair cycle control by estrogens: Catagen induction via estrogen receptor (ER)-α is checked by ERβ signaling

Ulrich Ohnemus, Murat Uenalan, Franziska Conrad, Bori Handjiski, Lars Mecklenburg, Motonobu Nakamura, José Inzunza, Jan Åke Gustafsson, Ralf Paus

Research output: Contribution to journalArticlepeer-review

65 Scopus citations

Abstract

Although 17β-estradiol (E2) is recognized as a potent hair growth modulator, our knowledge of estrogen function, signaling, and target genes in hair biology is still very limited. Between the two recognized estrogen receptors (ERs), ERα and ERβ, only ERα had been detected in murine skin. Here we show that ERα, ERβ, and ERβ ins are all expressed throughout the murine hair cycle, both at the protein and RNA level, but show distinct expression patterns. We confirm that topical E2 arrests murine pelage hair follicles in telogen and demonstrate that E2 is a potent inducer of premature catagen development. The ER antagonist ICI 182.780 does not induce anagen prematurely but accelerates anagen development and wave spreading in female mice. ERβ knockout mice display accelerated catagen development along with an increase in the number of apoptotic hair follicle keratinocytes. This suggests that, contrary to previous concepts, ERβ does indeed play a significant role in murine hair growth control: whereas the catagen-promoting properties of E2 are mediated via ERα, ERβ mainly may function as a silencer of ERα action in hair biology. These findings illustrate the complexity of hair growth modulation by estrogens and suggest that one key to more effective hair growth manipulation with ER ligands lies in the use of selective ERα or -β antagonists/agonists. Our study also underscores that the hair cycling response to estrogens offers an ideal model for studying the controls and dynamics of wave propagation in biological systems.

Original languageEnglish (US)
Pages (from-to)1214-1225
Number of pages12
JournalEndocrinology
Volume146
Issue number3
DOIs
StatePublished - Mar 2005
Externally publishedYes

ASJC Scopus subject areas

  • Endocrinology

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