The Ins and Outs of Mitochondrial Calcium

Author:

Finkel Toren1,Menazza Sara1,Holmström Kira M.1,Parks Randi J.1,Liu Julia1,Sun Junhui1,Liu Jie1,Pan Xin1,Murphy Elizabeth1

Affiliation:

1. From the Center for Molecular Medicine (T.F., K.M.H., Julia Liu, Jie Liu) and Systems Biology Center (S.M., R.J.P., J.S., E.M.), National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD; and Laboratory of Cell Biology, National Center of Biomedical Analysis, Beijing, China (X.P.).

Abstract

Calcium is thought to play an important role in regulating mitochondrial function. Evidence suggests that an increase in mitochondrial calcium can augment ATP production by altering the activity of calcium-sensitive mitochondrial matrix enzymes. In contrast, the entry of large amounts of mitochondrial calcium in the setting of ischemia-reperfusion injury is thought to be a critical event in triggering cellular necrosis. For many decades, the details of how calcium entered the mitochondria remained a biological mystery. In the past few years, significant progress has been made in identifying the molecular components of the mitochondrial calcium uniporter complex. Here, we review how calcium enters and leaves the mitochondria, the growing insight into the topology, stoichiometry and function of the uniporter complex, and the early lessons learned from some initial mouse models that genetically perturb mitochondrial calcium homeostasis.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine,Physiology

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