AI Article Synopsis

  • Autophagosomal membranes play a crucial role in various cell signaling networks related to survival and death, beyond just autophagy.
  • Inhibiting the completion of autophagosomes leads to immature membrane accumulation that activates caspase-8 in response to nutrient starvation through the intracellular death-inducing signaling complex (iDISC).
  • The research identifies NF-κB signaling and c-FLIP as factors that inhibit iDISC-mediated caspase-8 activation, suggesting that targeting autophagosomal membrane completion could shift processes from protective autophagy to cell death.

Article Abstract

Autophagosomal membranes are emerging as platforms for various cell survival and death signaling networks beyond autophagy. While autophagy-dependent cell death has been reported in response to a variety of stimuli, the underlying molecular mechanisms remain far from clear. Here, we demonstrate that inhibition of autophagosome completion by Atg2A/B deletion accumulates immature autophagosomal membranes that promote non-canonical caspase-8 activation in response to nutrient starvation via an intracellular death-inducing signaling complex (iDISC). Importantly, iDISC-induced caspase-8 dimerization and activation occurs on accumulated autophagosomal membranes and requires the LC3 conjugation machinery but is independent from the extrinsic pathway of apoptosis. Moreover, we have identified NF-κB signaling and c-FLIP as negative regulators of iDISC-mediated caspase-8 activation and apoptosis. Collectively, these findings reveal autophagosomal membrane completion as a novel target to switch cytoprotective autophagy to apoptosis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5686350PMC
http://dx.doi.org/10.1038/cdd.2017.133DOI Listing

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