Programmed Cell Death and Caspase Functions During Neural Development

Curr Top Dev Biol. 2015:114:159-84. doi: 10.1016/bs.ctdb.2015.07.016. Epub 2015 Sep 9.

Abstract

Programmed cell death (PCD) is a fundamental component of nervous system development. PCD serves as the mechanism for quantitative matching of the number of projecting neurons and their target cells through direct competition for neurotrophic factors in the vertebrate peripheral nervous system. In addition, PCD plays roles in regulating neural cell numbers, canceling developmental errors or noise, and tissue remodeling processes. These findings are mainly derived from genetic studies that prevent cells from dying by apoptosis, which is a major form of PCD and is executed by activation of evolutionarily conserved cysteine protease caspases. Recent studies suggest that caspase activation can be coordinated in time and space at multiple levels, which might underlie nonapoptotic roles of caspases in neural development in addition to apoptotic roles.

Keywords: Apoptosis; Caspase; Drosophila; Mouse; Nervous system; Neural tube closure; Neuroblasts; Programmed cell death; Sensory organ precursor; Signaling center.

Publication types

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

MeSH terms

  • Animals
  • Apoptosis* / physiology
  • Caspases / metabolism*
  • Cell Death
  • Cell Differentiation
  • Cell Lineage
  • Cell Survival
  • Drosophila / growth & development
  • Enzyme Activation
  • Eye / cytology
  • Eye / growth & development
  • Morphogenesis
  • Nervous System / cytology
  • Nervous System / growth & development*
  • Neurogenesis
  • Neuroglia / cytology
  • Neurons / cytology*

Substances

  • Caspases