articleMolecular and Cellular BiologyMar 31, 2006GREEN OA

Autocrine Tumor Necrosis Factor Alpha Links Endoplasmic Reticulum Stress to the Membrane Death Receptor Pathway through IRE1α-Mediated NF-κB Activation and Down-Regulation of TRAF2 Expression

Vanderbilt University Medical Center · University of Michigan–Ann Arbor · +1 more institution

PubMed
Indexed incrossrefpubmed

Abstract

NF-kappaB is critical for determining cellular sensitivity to apoptotic stimuli by regulating both mitochondrial and death receptor apoptotic pathways. The endoplasmic reticulum (ER) emerges as a new apoptotic signaling initiator. However, the mechanism by which ER stress activates NF-kappaB and its role in regulation of ER stress-induced cell death are largely unclear. Here, we report that, in response to ER stress, IKK forms a complex with IRE1alpha through the adapter protein TRAF2. ER stress-induced NF-kappaB activation is impaired in IRE1alpha knockdown cells and IRE1alpha(-/-) MEFs. We found, however, that inhibiting NF-kappaB significantly decreased ER stress-induced cell death in a caspase-8-dependent…

Citation impact

745
total citations
FWCI
10.15
Percentile
100%
References
45
Citations per year

Authors

5

Topics & keywords

Keywords
  • Unfolded protein response
  • TRAF2
  • Cell biology
  • Biology
  • Endoplasmic reticulum
  • Programmed cell death
  • Signal transduction
  • Tumor necrosis factor alpha
UN Sustainable Development Goals
  • Good health and well-being
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