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Review
. 2018 Dec:192:112-123.
doi: 10.1016/j.pharmthera.2018.07.001. Epub 2018 Jul 20.

Mitochondrial Ca2+ signaling

Affiliations
Review

Mitochondrial Ca2+ signaling

Trayambak Pathak et al. Pharmacol Ther. 2018 Dec.

Abstract

Mitochondrial Ca2+ regulation is crucial for bioenergetics and cellular signaling. The mechanisms controlling mitochondrial calcium homeostasis have been recently unraveled with the discovery of mitochondrial inner membrane proteins that regulate mitochondrial Ca2+ uptake and extrusion. Mitochondrial Ca2+ uptake depends on a large complex of proteins centered around the Ca2+ channel protein, mitochondrial Ca2+ uniporter (MCU) in close interactions with several regulatory subunits (MCUb, EMRE, MICU1, MICU2). Mitochondrial Ca2+ extrusion is mainly mediated by the mitochondrial Na+/Ca2+/Li+ exchanger (NCLX). Here, we review the major players of mitochondrial Ca2+ homeostasis and their physiological functions.

Keywords: Ca(2+) signaling; Cell metabolism; MCU; Mitochondria associated membranes; NCLX; Reactive oxygen species; physiology of mitochondrial Ca(2+).

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Conflict of interest statement

Conflict of Interest

The authors have no conflict of interest to declare.

Figures

Figure 1:
Figure 1:. Mitochondrial Ca2+ homeostasis: Ca2+ cycling between the cytosol, ER, and mitochondria.
Activation of phospholipase C (PLC)-coupled agonists produce the soluble cytosolic second messenger inositol-1,4,5 trisphosphate (ΓΡ3) which binds to its receptor, the IP3R, and cause Ca2+ release from the ER to the cytosol. Through mitochondria associated membranes (MAMs), Ca2+ released from IP3R crosses the OMM through VDAC and enters the intermembrane space (IMS) before reaching the mitochondrial matrix through MCU. Depletion of ER Ca2+ concentration also triggers the activation of store-operated Ca2+ entry (SOCE) into the cytosol across the plasma membrane through ORAI1 channels. Ca2+ entry through SOCE is buffered back into the ER by the action of sarcoplasmic/endoplasmic reticulum ATPase (SERCA) pumps or can be taken up by mitochondria through MCU.VDAC resides in the outer mitochondrial membrane (OMM) and brings Ca2+ in the intermembrane space (IMS) of mitochondria. Once Ca2+ concentration in the IMS is high, it is sensed by the gatekeeper proteins MICU1/MICU2 which disinhibit MCU allowing Ca2+ uptake into the mitochondrial matrix. Matrix Ca2+ is pumped back to the IMS through the Na+/Ca2+ exchange (NCLX) and Letml.
Figure 2:
Figure 2:. Components of the MCU complex and its regulation by Ca2+.
A) MCU, MICU1/2/3, EMRE, MCUR1, and MCUb form the Uniporter complex. When the Ca2+ concentration in mitochondrial intermembrane space (IMS) is low, MICU2 inhibits MCU activity. B) When the IMS Ca2+ concentration is high, Ca2+ binds to MICU1 and activates MCU to cause Ca2+ uptake into the mitochondrial matrix. EMRE is an essential subunit that is required for MCU function and helps tether MICU1/MICU2 to the MCU complex. The yellow dots represent Ca2+.

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