内质网
线粒体
细胞生物学
细胞器
线粒体膜转运蛋白
钙信号传导
化学
线粒体基质
生物
线粒体内膜
生物化学
信号转导
胞浆
酶
作者
Saverio Marchi,Mart Bittremieux,Sonia Missiroli,Claudia Morganti,Simone Patergnani,Luigi Sbano,Alessandro Rimessi,Martijn Kerkhofs,Jan B. Parys,Geert Bultynck,Carlotta Giorgi,Paolo Pinton
标识
DOI:10.1007/978-981-10-4567-7_4
摘要
The execution of proper Ca2+ signaling requires close apposition between the endoplasmic reticulum (ER) and mitochondria. Hence, Ca2+ released from the ER is "quasi-synaptically" transferred to mitochondrial matrix, where Ca2+ stimulates mitochondrial ATP synthesis by activating the tricarboxylic acid (TCA) cycle. However, when the Ca2+ transfer is excessive and sustained, mitochondrial Ca2+ overload induces apoptosis by opening the mitochondrial permeability transition pore. A large number of regulatory proteins reside at mitochondria-associated ER membranes (MAMs) to maintain the optimal distance between the organelles and to coordinate the functionality of both ER and mitochondrial Ca2+ transporters or channels. In this chapter, we discuss the different pathways involved in the regulation of ER-mitochondria Ca2+ flux and describe the activities of the various Ca2+ players based on their primary intra-organelle localization.
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