Mitochondrial calcium exchange in physiology and disease

The uptake of calcium into and extrusion of calcium from the mitochondrial matrix is a fundamental biological process that has critical effects on cellular metabolism, signaling, and survival. Disruption of mitochondrial calcium ( Ca ) cycling is implicated in numerous acquired diseases such as hear...

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:Physiological reviews Ročník 102; číslo 2; s. 893
Hlavní autoři: Garbincius, Joanne F, Elrod, John W
Médium: Journal Article
Jazyk:angličtina
Vydáno: United States 01.04.2022
Témata:
Animals
Calcium - metabolism
Calcium Channels - metabolism
Calcium Signaling - physiology
Calcium-Binding Proteins - genetics
Calcium-Binding Proteins - metabolism
Homeostasis - physiology
Humans
Mitochondria - metabolism
calcium
disease
NCLX
mitochondria
MCU
ISSN:1522-1210, 1522-1210
On-line přístup:Zjistit podrobnosti o přístupu
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo vytvoří štítek k tomuto záznamu!
Popis
Shrnutí:The uptake of calcium into and extrusion of calcium from the mitochondrial matrix is a fundamental biological process that has critical effects on cellular metabolism, signaling, and survival. Disruption of mitochondrial calcium ( Ca ) cycling is implicated in numerous acquired diseases such as heart failure, stroke, neurodegeneration, diabetes, and cancer and is genetically linked to several inherited neuromuscular disorders. Understanding the mechanisms responsible for Ca exchange therefore holds great promise for the treatment of these diseases. The past decade has seen the genetic identification of many of the key proteins that mediate mitochondrial calcium uptake and efflux. Here, we present an overview of the phenomenon of Ca transport and a comprehensive examination of the molecular machinery that mediates calcium flux across the inner mitochondrial membrane: the mitochondrial uniporter complex (consisting of MCU, EMRE, MICU1, MICU2, MICU3, MCUB, and MCUR1), NCLX, LETM1, the mitochondrial ryanodine receptor, and the mitochondrial permeability transition pore. We then consider the physiological implications of Ca flux and evaluate how alterations in Ca homeostasis contribute to human disease. This review concludes by highlighting opportunities and challenges for therapeutic intervention in pathologies characterized by aberrant Ca handling and by summarizing critical unanswered questions regarding the biology of Ca flux.
Bibliografie:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
ObjectType-Review-3
content type line 23
ISSN:1522-1210
1522-1210
DOI:10.1152/physrev.00041.2020