Control of KIT signalling in male germ cells: what can we learn from other systems?

Reproduction. 2009 Nov;138(5):743-57. doi: 10.1530/REP-08-0537. Epub 2009 Jun 30.

Abstract

The KIT ligand (KITL)/KIT-signalling system is among several pathways known to be essential for fertility. In the postnatal testis, the KIT/KITL interaction is crucial for spermatogonial proliferation, differentiation, survival and subsequent entry into meiosis. Hence, identification of endogenous factors that regulate KIT synthesis is important for understanding the triggers driving germ cell maturation. Although limited information is available regarding local factors in the testicular microenvironment that modulate KIT synthesis at the onset of spermatogenesis, knowledge from other systems could be used as a basis for identifying how KIT function is regulated in germ cells. This review describes the known regulators of KIT, including transcription factors implicated in KIT promoter regulation. In addition, specific downstream outcomes in biological processes that KIT orchestrates are addressed. These are discussed in relationship to current knowledge of mammalian germ cell development.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Gene Expression Regulation, Developmental
  • Germ Cells / metabolism
  • Humans
  • Male
  • Mammals / genetics
  • Mammals / growth & development
  • Mammals / metabolism
  • Models, Biological
  • Proto-Oncogene Proteins c-kit / genetics
  • Proto-Oncogene Proteins c-kit / metabolism*
  • Proto-Oncogene Proteins c-kit / physiology
  • Signal Transduction / genetics
  • Spermatogenesis / genetics
  • Spermatogenesis / physiology
  • Spermatozoa / metabolism*
  • Stem Cell Factor / genetics
  • Stem Cell Factor / metabolism
  • Stem Cell Factor / physiology

Substances

  • Stem Cell Factor
  • Proto-Oncogene Proteins c-kit