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TRAF family proteins interact with the common neurotrophin receptor and modulate apoptosis induction.

The common neurotrophin receptor, p75(NTR), has been shown to signal in the absence of Trk tyrosine kinase receptors, including induction of neural apoptosis and activation of NF-kappaB. However, the mechanisms by which p75(NTR) initiates these intracellular signal transduction pathways are unknown. Here we report interactions between p75(NTR) and the six members of TRAF (tumor necrosis factor receptor-associated factors) family proteins. The binding of different TRAF proteins to p75(NTR) was mapped to distinct regions in p75(NTR). Furthermore, TRAF4 interacted with dimeric p75(NTR), whereas TRAF2 interacted preferentially with monomeric p75(NTR). TRAF2-p75(NTR), TRAF4-p75(NTR), and TRAF6-p75(NTR) interactions modulated p75(NTR)-induced cell death and NF-kappaB activation with contrasting effects. Coexpression of TRAF2 with p75(NTR) enhanced cell death, whereas coexpression of TRAF6 was cytoprotective. Furthermore, overexpression of TRAF4 abrogated the ability of dimerization to prevent the induction of apoptosis normally mediated by monomeric p75(NTR). TRAF4 also inhibited the NF-kappaB response, whereas TRAF2 and TRAF6 enhanced p75(NTR)-induced NF-kappaB activation. These results demonstrate that TRAF family proteins interact with p75(NTR) and differentially modulate its NF-kappaB activation and cell death induction.

Pubmed ID: 10514511

Authors

  • Ye X
  • Mehlen P
  • Rabizadeh S
  • VanArsdale T
  • Zhang H
  • Shin H
  • Wang JJ
  • Leo E
  • Zapata J
  • Hauser CA
  • Reed JC
  • Bredesen DE

Journal

The Journal of biological chemistry

Publication Data

October 15, 1999

Associated Grants

  • Agency: NCI NIH HHS, Id: CA69381
  • Agency: NINDS NIH HHS, Id: NS33376
  • Agency: NINDS NIH HHS, Id: NS35155

Mesh Terms

  • Apoptosis
  • Base Sequence
  • Biopolymers
  • Cell Line
  • DNA Primers
  • Humans
  • NF-kappa B
  • Protein Binding
  • Receptors, Nerve Growth Factor
  • Receptors, Tumor Necrosis Factor
  • Recombinant Fusion Proteins
  • Signal Transduction