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
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
- FWCI
- 10.15
- Percentile
- 100%
- References
- 45
Authors
5Topics & keywords
- Unfolded protein response
- TRAF2
- Cell biology
- Biology
- Endoplasmic reticulum
- Programmed cell death
- Signal transduction
- Tumor necrosis factor alpha
- Good health and well-being