| Literature DB >> 28815521 |
Saverio Marchi1, Mart Bittremieux2, Sonia Missiroli1, Claudia Morganti1, Simone Patergnani1, Luigi Sbano1, Alessandro Rimessi1, Martijn Kerkhofs2, Jan B Parys2, Geert Bultynck2, Carlotta Giorgi3, Paolo Pinton4.
Abstract
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.Entities:
Keywords: Apoptosis; Autophagy; Calcium; Cell death; ER-mitochondria contact sites; Endoplasmic reticulum (ER); Mitochondria; Mitochondria associated membranes (MAMs); ROS
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Year: 2017 PMID: 28815521 DOI: 10.1007/978-981-10-4567-7_4
Source DB: PubMed Journal: Adv Exp Med Biol ISSN: 0065-2598 Impact factor: 2.622