期刊
JOURNAL OF CELL SCIENCE
卷 129, 期 12, 页码 2317-2328出版社
COMPANY BIOLOGISTS LTD
DOI: 10.1242/jcs.179127
关键词
Apoptosis; Endoplasmic reticulum; IRE1; JNK; Stress response; Unfolded protein response
类别
资金
- European Community [201608]
- Diabetes UK [BDA 09/0003949]
- Parkinson's UK [H-1004]
- Diabetes UK [09/0003949] Funding Source: researchfish
- Parkinson's UK [H-1004] Funding Source: researchfish
Accumulation of unfolded proteins in the endoplasmic reticulum (ER) activates the unfolded protein response (UPR). In mammalian cells, UPR signals generated by several ER-membrane-resident proteins, including the bifunctional protein kinase endoribonuclease IRE1 alpha, control cell survival and the decision to execute apoptosis. Processing of XBP1 mRNA by the RNase domain of IRE1a promotes survival of ER stress, whereas activation of the mitogen-activated protein kinase JNK family by IRE1 alpha late in the ER stress response promotes apoptosis. Here, we show that activation of JNK in the ER stress response precedes activation of XBP1. This activation of JNK is dependent on IRE1 alpha and TRAF2 and coincides with JNK-dependent induction of expression of several antiapoptotic genes, including cIap1 (also known as Birc2), cIap2 (also known as Birc3), Xiap and Birc6. ER-stressed Jnk1(-/-) Jnk2(-/-) (Mapk8(-/-) Mapk9(-/-)) mouse embryonic fibroblasts (MEFs) display more pronounced mitochondrial permeability transition and increased caspase 3/7 activity compared to wild-type MEFs. Caspase 3/7 activity is also elevated in ER-stressed cIap1(-/-) cIap2(-/-) and Xiap(-/-) MEFs. These observations suggest that JNK-dependent transcriptional induction of several inhibitors of apoptosis contributes to inhibiting apoptosis early in the ER stress response.
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