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Knock-out of the neural death effector domain protein PEA-15 demonstrates that its expression protects astrocytes from TNFα-induced apoptosis

  • Daniel Kitsberg
  • , Etienne Formstecher
  • , Mireille Fauquet
  • , Miroslav Kubes
  • , Jocelyne Cordier
  • , Brigitte Canton
  • , Guo Hua Pan
  • , Malvyne Rolli
  • , Jacques Glowinski
  • , Hervé Chneiweiss
  • Harvard Medical School
  • Alamone Laboratories
  • Collège de France
  • Inst. Natl. Sante la Rech. Med. U114
  • Institute of Virology Slovak Academy of Sciences
  • Department of Pathology
  • University of Michigan Medical School
  • Genentech Inc.

Research output: Contribution to journal › Article › peer-review

130 Citations (Scopus)

Abstract

Apoptosis is a very general phenomenon, but only a few reports concern astrocytes. Indeed, astrocytes express receptors for tumor necrosis factor (TNF) α, a cytokine demonstrated on many cells and tissues to mediate apoptosis after recruitment of adaptor proteins containing a death effector domain (DED). PEA-15 is a DED-containing protein prominently expressed in the CNS and particularly abundant in astrocytes. This led us to investigate if PEA-15 expression could be involved in astrocytic protection against deleterious effects of TNF. In vitro assays evidence that PEA-15 may bind to DED-containing protein FADD and caspase-8 known to be apical adaptors of the TNF apoptotic signaling. After generation of PEA-15 null mutant mice, our results demonstrate that PEA-15 expression increases astrocyte survival after exposure to TNF.

Original languageEnglish
Pages (from-to)8244-8251
Number of pages8
JournalJournal of Neuroscience
Volume19
Issue number19
DOIs
Publication statusPublished - 1 Oct 1999
Externally publishedYes

Keywords

  • Apoptosis
  • Astrocytes
  • Caspase
  • Death effector domain
  • FADD
  • PEA-15
  • TNFα

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