蛋白质稳态
内质网
未折叠蛋白反应
细胞生物学
钙信号传导
钙
平衡
线粒体
蛋白质折叠
信号转导
化学
生物
有机化学
作者
Amado Carreras‐Sureda,Philippe Pihán,Claudio Hetz
出处
期刊:Cell Calcium
[Elsevier]
日期:2018-03-01
卷期号:70: 24-31
被引量:229
标识
DOI:10.1016/j.ceca.2017.08.004
摘要
Endoplasmic reticulum (ER) calcium signaling is implicated in a myriad of coordinated cellular processes. The ER calcium content is tightly regulated as it allows a favorable environment for protein folding, in addition to operate as a major reservoir for fast and specific release of calcium. Altered ER homeostasis impacts protein folding, activating the unfolded protein response (UPR) as a rescue mechanism to restore proteostasis. ER calcium release impacts mitochondrial metabolism and also fine-tunes the threshold to undergo apoptosis under chronic stress. The global coordination between UPR signaling and energetic demands takes place at mitochondrial associated membranes (MAMs), specialized subdomains mediating interorganelle communication. Here we discuss current models explaining the functional relationship between ER homeostasis and various cellular responses to coordinate proteostasis and metabolic maintenance.
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