Mouse models of alopecia: identifying structural genes that are baldly needed

Trends Mol Med. 2003 Feb;9(2):79-84. doi: 10.1016/s1471-4914(02)00025-4.

Abstract

The mature hair follicle undergoes a unique developmental cycle, in which phases of growth are interspersed with phases of involution and rest. The main effectors of this cycle are skin epithelial stem cells that reside in a specialized compartment of the follicle. Defects in this cycle, or in the structure of the hair produced, often result in alopecia (partial or complete hair loss), a condition that affects a significant fraction of the population. Here we discuss transgenic mouse models that exhibit alopecia as a primary phenotype, resulting from the inactivation of genes encoding structural proteins.

Publication types

  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Alopecia / genetics*
  • Alopecia / physiopathology
  • Animals
  • Cathepsins / genetics
  • Cell Adhesion Molecules / genetics
  • DNA-Binding Proteins / genetics
  • Forkhead Transcription Factors
  • Hair Follicle / growth & development*
  • Hair Follicle / pathology
  • Homeodomain Proteins / genetics
  • Keratins / genetics
  • Mice
  • Mice, Knockout
  • Mice, Transgenic
  • Models, Animal
  • Transcription Factors / genetics

Substances

  • Cell Adhesion Molecules
  • DNA-Binding Proteins
  • Forkhead Transcription Factors
  • Homeodomain Proteins
  • Hoxc13 protein, mouse
  • Transcription Factors
  • Whn protein
  • Keratins
  • Cathepsins