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.
机构:
Univ Sci Philadelphia, Philadelphia, PA 19104 USA
Access Grp, W Chester, PA USA
Mercy LIFE, Philadelphia, PA USAUniv Sci Philadelphia, Philadelphia, PA 19104 USA
Stefanacci, Richard G.
Haimowitz, Dan
论文数: 0引用数: 0
h-index: 0
机构:
Arden Courts Yardley, Yardley, PA USA
Brunswick Attleboro, Langhorne, PA USAUniv Sci Philadelphia, Philadelphia, PA 19104 USA
机构:
Texas A&M Univ, Coll Vet Med & Biomed Sci, Dept Large Anim Clin Sci, College Stn, TX 77843 USATexas A&M Univ, Coll Vet Med & Biomed Sci, Dept Large Anim Clin Sci, College Stn, TX 77843 USA