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Endoplasmic reticulum stress: cell life and death decisions

期刊

JOURNAL OF CLINICAL INVESTIGATION
卷 115, 期 10, 页码 2656-2664

出版社

AMER SOC CLINICAL INVESTIGATION INC
DOI: 10.1172/JCI26373

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资金

  1. NIA NIH HHS [R01 AG015393, AG15393] Funding Source: Medline
  2. NINDS NIH HHS [F32 NS047855, NS047855] Funding Source: Medline

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Disturbances in the normal functions of the ER lead to an evolutionarily conserved cell stress response, the unfolded protein response, which is aimed initially at compensating for damage but can eventually trigger cell death if ER dysfunction is severe or prolonged. The mechanisms by which ER stress leads to cell death remain enigmatic, with multiple potential participants described but little clarity about which specific death effectors dominate in particular cellular contexts. Important roles for ER-initiated cell death pathways have been recognized for several diseases, including hypoxia, ischemia/reperfusion injury, neurodegeneration, heart disease, and diabetes.

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