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      MICU3 is a tissue-specific enhancer of mitochondrial calcium uptake

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          Abstract

          The versatility and universality of Ca 2+ as intracellular messenger is guaranteed by the compartmentalization of changes in [Ca 2+]. In this context, mitochondrial Ca 2+ plays a central role, by regulating both specific organelle functions and global cellular events. This versatility is also guaranteed by a cell type-specific Ca 2+ signaling toolkit controlling specific cellular functions. Accordingly, mitochondrial Ca 2+ uptake is mediated by a multimolecular structure, the MCU complex, which differs among various tissues. Its activity is indeed controlled by different components that cooperate to modulate specific channeling properties. We here investigate the role of MICU3, an EF-hand containing protein expressed at high levels especially in brain. We show that MICU3 forms a disulfide bond-mediated dimer with MICU1, but not with MICU2, and it acts as enhancer of MCU-dependent mitochondrial Ca 2+ uptake. Silencing of MICU3 in primary cortical neurons impairs Ca 2+ signals elicited by synaptic activity, thus suggesting a specific role in regulating neuronal function.

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          Most cited references56

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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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              MICU1 encodes a mitochondrial EF hand protein required for Ca2+ uptake

              Mitochondrial calcium uptake plays a central role in cell physiology by stimulating ATP production, shaping cytosolic calcium transients, and regulating cell death. The biophysical properties of mitochondrial calcium uptake have been studied in detail, but the underlying proteins remain elusive. Here, we utilize an integrative strategy to predict human genes involved in mitochondrial calcium entry based on clues from comparative physiology, evolutionary genomics, and organelle proteomics. RNA interference against 13 top candidates highlighted one gene that we now call mitochondrial calcium uptake 1 (MICU1). Silencing MICU1 does not disrupt mitochondrial respiration or membrane potential but abolishes mitochondrial calcium entry in intact and permeabilized cells, and attenuates the metabolic coupling between cytosolic calcium transients and activation of matrix dehydrogenases. MICU1 is associated with the organelle’s inner membrane and has two canonical EF hands that are essential for its activity, suggesting a role in calcium sensing. MICU1 represents the founding member of a set of proteins required for high capacity mitochondrial calcium entry. Its discovery may lead to the complete molecular characterization of mitochondrial calcium uptake pathways, and offers genetic strategies for understanding their contribution to normal physiology and disease.
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                Author and article information

                Journal
                9437445
                20326
                Cell Death Differ
                Cell Death Differ.
                Cell death and differentiation
                1350-9047
                1476-5403
                28 March 2018
                03 May 2018
                03 November 2018
                : 10.1038/s41418-018-0113-8
                Affiliations
                [1 ]Department of Biomedical Sciences, University of Padova, Via Ugo Bassi 58B, 35131 Padova, Italy
                Author notes
                [2]

                Present address: Max Planck Institute for Biology and Aging, Cologne, Germany. Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), Center for Molecular Medicine (CMMC), University of Cologne, Cologne, Germany

                [3]

                Present address: Feil Family Brain and Mind Research Institute, Weill Cornell Medical College, 401 East 61st Street, New York, NY 10065, United States

                [4]

                Co-first authors

                [5 ]Corresponding authors: Contact information: Diego De Stefani, Department of Biomedical Sciences, University of Padova, Via Ugo Bassi 58/B, 35131 Padova, Italy, Phone: +390498276029, diego.destefani@ 123456gmail.com or Rosario Rizzuto, Department of Biomedical Sciences, University of Padova, Via Ugo Bassi 58/B, 35131 Padova, Italy, Phone: +390498273001, rosario.rizzuto@ 123456unipd.it
                Article
                EMS76766
                10.1038/s41418-018-0113-8
                6124646
                29725115
                7a970e27-e056-498b-b2eb-a30e227583f5

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                Cell biology
                Cell biology

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