Stimulation of Hair Growth by Small Molecules that Activate Autophagy

Cell Rep. 2019 Jun 18;27(12):3413-3421.e3. doi: 10.1016/j.celrep.2019.05.070.

Abstract

Hair plays important roles, ranging from the conservation of body heat to the preservation of psychological well-being. Hair loss or alopecia affects millions worldwide, but methods that can be used to regrow hair are lacking. We report that quiescent (telogen) hair follicles can be stimulated to initiate anagen and hair growth by small molecules that activate autophagy, including the metabolites α-ketoglutarate (α-KG) and α-ketobutyrate (α-KB), and the prescription drugs rapamycin and metformin, which impinge on mTOR and AMPK signaling. Stimulation of hair growth by these agents is blocked by specific autophagy inhibitors, suggesting a mechanistic link between autophagy and hair regeneration. Consistently, increased autophagy is detected upon anagen entry during the natural hair follicle cycle, and oral α-KB prevents hair loss in aged mice. Our finding that anagen can be pharmacologically activated in telogen skin when natural anagen-inducing signal(s) are absent has implications for the treatment of hair loss patients.

Keywords: AMPK; autophagy; hair loss; hair regeneration; mTOR; metabolite; metformin; rapamycin; α-ketobutyrate; α-ketoglutarate.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • AMP-Activated Protein Kinases / metabolism
  • Aging / drug effects
  • Aging / metabolism
  • Aging / physiology
  • Allyl Compounds / pharmacology
  • Alopecia / drug therapy*
  • Alopecia / genetics
  • Alopecia / metabolism
  • Animals
  • Autophagy / drug effects*
  • Autophagy / genetics
  • Butyrates / pharmacology
  • Cell Division / drug effects
  • Cell Division / genetics
  • Female
  • Hair / drug effects*
  • Hair / growth & development
  • Hair Follicle / drug effects*
  • Hair Follicle / metabolism
  • Ketoglutaric Acids / pharmacology
  • Male
  • Metformin / pharmacology
  • Mice
  • Mice, Inbred C57BL
  • Oligomycins / pharmacology
  • Quinazolines / pharmacology
  • Signal Transduction / drug effects
  • Signal Transduction / genetics
  • Sirolimus / pharmacology
  • TOR Serine-Threonine Kinases / genetics
  • TOR Serine-Threonine Kinases / metabolism*

Substances

  • 6-bromo-4-allylamino-quinazoline
  • Allyl Compounds
  • Butyrates
  • Ketoglutaric Acids
  • Oligomycins
  • Quinazolines
  • alpha-ketobutyric acid
  • Metformin
  • mTOR protein, mouse
  • TOR Serine-Threonine Kinases
  • AMP-Activated Protein Kinases
  • Sirolimus