Interactive nervous system development: control of cell survival in Drosophila

Trends Neurosci. 2002 Jul;25(7):365-70. doi: 10.1016/s0166-2236(02)02186-0.

Abstract

The non-autonomous control of cell survival has long been thought to be a mechanism of adjusting cell populations in the vertebrate nervous system, enabling connectivity and myelination to produce a functional brain. Despite cellular evidence that analogous mechanisms occur in invertebrates, scepticism has long reigned over whether they operate in model organisms such as Drosophila. This has led to speculation that there are inherent differences between the development and evolution of simple brains and the brains of vertebrates. The great paradox has, until recently, been the absence of molecular evidence of trophic factors in Drosophila. Recent data have finally shown that EGFR (epidermal-growth-factor receptor) ligands function in the Drosophila CNS to maintain glial survival. Trophic interactions are, thus, a general mechanism of nervous system development.

Publication types

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

MeSH terms

  • Animals
  • Body Patterning / physiology
  • Cell Communication / physiology
  • Cell Differentiation / physiology
  • Cell Survival / physiology*
  • Drosophila melanogaster / cytology
  • Drosophila melanogaster / embryology*
  • Drosophila melanogaster / metabolism
  • ErbB Receptors / genetics
  • ErbB Receptors / metabolism*
  • Nerve Growth Factors / genetics
  • Nerve Growth Factors / metabolism
  • Nervous System / cytology
  • Nervous System / embryology*
  • Nervous System / metabolism
  • Neuroglia / cytology
  • Neuroglia / metabolism*
  • Neurons / cytology
  • Neurons / metabolism*

Substances

  • Nerve Growth Factors
  • ErbB Receptors