NGF deprivation-induced gene expression: after ten years, where do we stand?

Prog Brain Res. 2004:146:111-26. doi: 10.1016/S0079-6123(03)46008-1.

Abstract

Nerve growth factor (NGF) is required for the survival of developing sympathetic and sensory neurons. In the absence of NGF, these neurons undergo protein synthesis-dependent apoptosis. Ten years have gone by since the first reports of specific genes being upregulated during NGF deprivation-induced cell death. Over the last decade, a few additional genes (DP5, Bim, SM-20) have been added to a list that began with cyclin D1 and c-jun. In this chapter, we discuss the evidence that these genes act as regulators of neuronal cell death. We also suggest a hypothesis for how one gene, SM-20, may function to suppress a self-protection mechanism in NGF-deprived neurons.

Publication types

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

MeSH terms

  • Animals
  • Apoptosis Regulatory Proteins
  • Cell Death / physiology*
  • Cell Division
  • Cell Survival / physiology
  • Cells, Cultured
  • Cyclin D1 / genetics
  • Cyclin D1 / metabolism
  • Cyclin-Dependent Kinases / metabolism
  • DNA-Binding Proteins*
  • Dioxygenases
  • Gene Expression / physiology*
  • History, 20th Century
  • History, 21st Century
  • Humans
  • Hydroxylation
  • Hypoxia-Inducible Factor-Proline Dioxygenases
  • Immediate-Early Proteins / genetics
  • Immediate-Early Proteins / metabolism
  • Immunohistochemistry
  • Nerve Growth Factors / deficiency*
  • Nerve Growth Factors / history
  • Nerve Growth Factors / physiology
  • Neurons / cytology*
  • Neuropeptides / genetics
  • Neuropeptides / metabolism
  • Nuclear Proteins / metabolism
  • Peptide Fragments / metabolism
  • Procollagen-Proline Dioxygenase / chemistry
  • Procollagen-Proline Dioxygenase / metabolism
  • Proto-Oncogene Proteins / metabolism
  • Proto-Oncogene Proteins c-jun / genetics
  • Proto-Oncogene Proteins c-jun / metabolism

Substances

  • Apoptosis Regulatory Proteins
  • Bax protein (53-86)
  • DNA-Binding Proteins
  • HRK protein, human
  • Hrk protein, rat
  • Immediate-Early Proteins
  • Nerve Growth Factors
  • Neuropeptides
  • Nuclear Proteins
  • Peptide Fragments
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-jun
  • Cyclin D1
  • Dioxygenases
  • EGLN1 protein, human
  • Procollagen-Proline Dioxygenase
  • EGLN2 protein, human
  • Egln1 protein, mouse
  • Hypoxia-Inducible Factor-Proline Dioxygenases
  • Cyclin-Dependent Kinases