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PUMA amplifies necroptosis signaling by activating cytosolic DNA sensors.


ABSTRACT: Necroptosis, a form of regulated necrotic cell death, is governed by RIP1/RIP3-mediated activation of MLKL. However, the signaling process leading to necroptotic death remains to be elucidated. In this study, we found that PUMA, a proapoptotic BH3-only Bcl-2 family member, is transcriptionally activated in an RIP3/MLKL-dependent manner following induction of necroptosis. The induction of PUMA, which is mediated by autocrine TNF-? and enhanced NF-?B activity, contributes to necroptotic death in RIP3-expressing cells with caspases inhibited. On induction, PUMA promotes the cytosolic release of mitochondrial DNA and activation of the DNA sensors DAI/Zbp1 and STING, leading to enhanced RIP3 and MLKL phosphorylation in a positive feedback loop. Furthermore, deletion of PUMA partially rescues necroptosis-mediated developmental defects in FADD-deficient embryos. Collectively, our results reveal a signal amplification mechanism mediated by PUMA and cytosolic DNA sensors that is involved in TNF-driven necroptotic death in vitro and in vivo.

SUBMITTER: Chen D 

PROVIDER: S-EPMC5899441 | biostudies-literature | 2018 Apr

REPOSITORIES: biostudies-literature

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PUMA amplifies necroptosis signaling by activating cytosolic DNA sensors.

Chen Dongshi D   Tong Jingshan J   Yang Liheng L   Wei Liang L   Stolz Donna B DB   Yu Jian J   Zhang Jianke J   Zhang Lin L  

Proceedings of the National Academy of Sciences of the United States of America 20180326 15


Necroptosis, a form of regulated necrotic cell death, is governed by RIP1/RIP3-mediated activation of MLKL. However, the signaling process leading to necroptotic death remains to be elucidated. In this study, we found that <i>PUMA</i>, a proapoptotic BH3-only Bcl-2 family member, is transcriptionally activated in an RIP3/MLKL-dependent manner following induction of necroptosis. The induction of PUMA, which is mediated by autocrine TNF-α and enhanced NF-κB activity, contributes to necroptotic dea  ...[more]

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