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UPR, autophagy, and mitochondria crosstalk underlies the ER stress response
被引:825
|作者:
Senft, Daniela
[1
]
Ronai, Ze'ev A.
[1
]
机构:
[1] Sanford Burnham Med Res Inst, La Jolla, CA 92037 USA
关键词:
ER stress;
UPR;
ubiquitin;
hypoxia;
autophagy;
mitochondria;
ENDOPLASMIC-RETICULUM STRESS;
UNFOLDED PROTEIN RESPONSE;
INDUCED CELL-DEATH;
UBIQUITIN LIGASE ACTIVITY;
E3;
LIGASE;
TRANSCRIPTION FACTOR;
PARKINSONS-DISEASE;
MEDIATED APOPTOSIS;
ACTIVATE PARKIN;
GENE-EXPRESSION;
D O I:
10.1016/j.tibs.2015.01.002
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Cellular stress, induced by external or internal cues, activates several well-orchestrated processes aimed at either restoring cellular homeostasis or committing to cell death. Those processes include the unfolded protein response (UPR), autophagy, hypoxia, and mitochondrial function, which are part of the global endoplasmic reticulum (ER) stress (ERS) response. When one of the ERS elements is impaired, as often occurs under pathological conditions, overall cellular homeostasis may be perturbed. Further, activation of the UPR could trigger changes in mitochondrial function or autophagy, which could modulate the UPR, exemplifying crosstalk processes. Among the numerous factors that control the magnitude or duration of these processes are ubiquitin ligases, which govern overall cellular stress outcomes. Here we summarize crosstalk among the fundamental processes governing ERS responses.
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页码:141 / 148
页数:8
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