Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2016 Oct;1863(10):2457-64.
doi: 10.1016/j.bbamcr.2016.03.006. Epub 2016 Mar 8.

Molecular structure and pathophysiological roles of the Mitochondrial Calcium Uniporter

Affiliations
Free article
Review

Molecular structure and pathophysiological roles of the Mitochondrial Calcium Uniporter

Cristina Mammucari et al. Biochim Biophys Acta. 2016 Oct.
Free article

Abstract

Mitochondrial Ca(2+) uptake regulates a wide array of cell functions, from stimulation of aerobic metabolism and ATP production in physiological settings, to induction of cell death in pathological conditions. The molecular identity of the Mitochondrial Calcium Uniporter (MCU), the highly selective channel responsible for Ca(2+) entry through the IMM, has been described less than five years ago. Since then, research has been conducted to clarify the modulation of its activity, which relies on the dynamic interaction with regulatory proteins, and its contribution to the pathophysiology of organs and tissues. Particular attention has been placed on characterizing the role of MCU in cardiac and skeletal muscles. In this review we summarize the molecular structure and regulation of the MCU complex in addition to its pathophysiological role, with particular attention to striated muscle tissues. This article is part of a Special Issue entitled: Mitochondrial Channels edited by Pierre Sonveaux, Pierre Maechler and Jean-Claude Martinou.

Keywords: Cardiac muscle; Mitochondrial Calcium Uniporter; Mitochondrial calcium uptake; Skeletal muscle.

PubMed Disclaimer

Publication types

MeSH terms

LinkOut - more resources