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      Release and uptake mechanisms of vesicular Ca 2+ stores

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          Abstract

          Cells utilize calcium ions (Ca 2+) to signal almost all aspects of cellular life, ranging from cell proliferation to cell death, in a spatially and temporally regulated manner. A key aspect of this regulation is the compartmentalization of Ca 2+ in various cytoplasmic organelles that act as intracellular Ca 2+ stores. Whereas Ca 2+ release from the large-volume Ca 2+ stores, such as the endoplasmic reticulum (ER) and Golgi apparatus, are preferred for signal transduction, Ca 2+ release from the small-volume individual vesicular stores that are dispersed throughout the cell, such as lysosomes, may be more useful in local regulation, such as membrane fusion and individualized vesicular movements. Conceivably, these two types of Ca 2+ stores may be established, maintained or refilled via distinct mechanisms. ER stores are refilled through sustained Ca 2+ influx at ER-plasma membrane (PM) membrane contact sites (MCSs). In this review, we discuss the release and refilling mechanisms of intracellular small vesicular Ca 2+ stores, with a special focus on lysosomes. Recent imaging studies of Ca 2+ release and organelle MCSs suggest that Ca 2+ exchange may occur between two types of stores, such that the small stores acquire Ca 2+ from the large stores via ER-vesicle MCSs. Hence vesicular stores like lysosomes may be viewed as secondary Ca 2+ stores in the cell.

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          Most cited references70

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          Calcium signaling.

          Calcium ions (Ca(2+)) impact nearly every aspect of cellular life. This review examines the principles of Ca(2+) signaling, from changes in protein conformations driven by Ca(2+) to the mechanisms that control Ca(2+) levels in the cytoplasm and organelles. Also discussed is the highly localized nature of Ca(2+)-mediated signal transduction and its specific roles in excitability, exocytosis, motility, apoptosis, and transcription.
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            Mitochondria as sensors and regulators of calcium signalling.

            During the past two decades calcium (Ca(2+)) accumulation in energized mitochondria has emerged as a biological process of utmost physiological relevance. Mitochondrial Ca(2+) uptake was shown to control intracellular Ca(2+) signalling, cell metabolism, cell survival and other cell-type specific functions by buffering cytosolic Ca(2+) levels and regulating mitochondrial effectors. Recently, the identity of mitochondrial Ca(2+) transporters has been revealed, opening new perspectives for investigation and molecular intervention.
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              Store-Operated Calcium Channels.

              Store-operated calcium channels (SOCs) are a major pathway for calcium signaling in virtually all metozoan cells and serve a wide variety of functions ranging from gene expression, motility, and secretion to tissue and organ development and the immune response. SOCs are activated by the depletion of Ca(2+) from the endoplasmic reticulum (ER), triggered physiologically through stimulation of a diverse set of surface receptors. Over 15 years after the first characterization of SOCs through electrophysiology, the identification of the STIM proteins as ER Ca(2+) sensors and the Orai proteins as store-operated channels has enabled rapid progress in understanding the unique mechanism of store-operate calcium entry (SOCE). Depletion of Ca(2+) from the ER causes STIM to accumulate at ER-plasma membrane (PM) junctions where it traps and activates Orai channels diffusing in the closely apposed PM. Mutagenesis studies combined with recent structural insights about STIM and Orai proteins are now beginning to reveal the molecular underpinnings of these choreographic events. This review describes the major experimental advances underlying our current understanding of how ER Ca(2+) depletion is coupled to the activation of SOCs. Particular emphasis is placed on the molecular mechanisms of STIM and Orai activation, Orai channel properties, modulation of STIM and Orai function, pharmacological inhibitors of SOCE, and the functions of STIM and Orai in physiology and disease.
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                Author and article information

                Contributors
                mnfxh@zjut.edu.cn
                haoxingx@umich.edu
                Journal
                Protein Cell
                Protein Cell
                Protein & Cell
                Higher Education Press (Beijing )
                1674-800X
                1674-8018
                16 March 2018
                16 March 2018
                January 2019
                : 10
                : 1
                : 8-19
                Affiliations
                [1 ]ISNI 0000 0004 1761 325X, GRID grid.469325.f, Collaborative Innovation Center of Yangtze River Delta Region Green Pharmaceuticals, College of Pharmaceutical Sciences, , Zhejiang University of Technology, ; Hangzhou, 310014 China
                [2 ]ISNI 0000000086837370, GRID grid.214458.e, The Department of Molecular, Cellular, and Developmental Biology, , University of Michigan, ; Ann Arbor, MI 48109 USA
                Author information
                http://orcid.org/0000-0002-6425-8495
                http://orcid.org/0000-0001-5701-4196
                http://orcid.org/0000-0002-7132-7284
                http://orcid.org/0000-0002-1645-6606
                http://orcid.org/0000-0003-3561-4654
                Article
                523
                10.1007/s13238-018-0523-x
                6321814
                29549599
                0768ddc9-9ff6-4b5b-927b-37c786f7d5bb
                © The Author(s) 2018

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

                History
                : 29 December 2017
                : 5 February 2018
                Categories
                Review
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                © Higher Education Press and Springer-Verlag GmbH Germany, part of Springer Nature 2019

                ca2+ stores,lysosomes,vesicles,refilling,organelle membrane contact sites (mcss)

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