Starkov 2010 FEBS J: Difference between revisions
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{{Publication | {{Publication | ||
|title=Starkov AA (2010) The molecular identity of the mitochondrial Ca2+ sequestration system. FEBS J. 277: 3652-63. | |title=Starkov AA (2010) The molecular identity of the mitochondrial Ca2+ sequestration system. FEBS J. 277:3652-63. | ||
|info=[http://www.ncbi.nlm.nih.gov/pubmed/20659159 PMID: 20659159] | |info=[http://www.ncbi.nlm.nih.gov/pubmed/20659159 PMID: 20659159 Open Access] | ||
|authors=Starkov AA | |authors=Starkov AA | ||
|year=2010 | |year=2010 | ||
|journal=FEBS J | |journal=FEBS J | ||
|abstract=There is ample evidence to suggest that a dramatic decrease in mitochondrial Ca(2+) retention may contribute to the cell death associated with stroke, excitotoxicity, ischemia and reperfusion, and neurodegenerative diseases. Mitochondria from all studied tissues can accumulate and store Ca(2+) , but the maximum Ca(2+) storage capacity varies widely and exhibits striking tissue specificity. There is currently no explanation for this fact. Precipitation of Ca(2+) and phosphate in the mitochondrial matrix has been suggested to be the major form of storage of accumulated Ca(2+) in mitochondria. How this precipitate is formed is not known. The molecular identity of almost all proteins involved in Ca(2+) transport, storage and formation of the permeability transition pore is also unknown. This review summarizes studies aimed at identifying these proteins, and describes the properties of a known mitochondrial protein that may be involved in Ca(2+) transport and the structure of the permeability transition pore. | |abstract=There is ample evidence to suggest that a dramatic decrease in mitochondrial Ca(2+) retention may contribute to the cell death associated with stroke, excitotoxicity, ischemia and reperfusion, and neurodegenerative diseases. Mitochondria from all studied tissues can accumulate and store Ca(2+) , but the maximum Ca(2+) storage capacity varies widely and exhibits striking tissue specificity. There is currently no explanation for this fact. Precipitation of Ca(2+) and phosphate in the mitochondrial matrix has been suggested to be the major form of storage of accumulated Ca(2+) in mitochondria. How this precipitate is formed is not known. The molecular identity of almost all proteins involved in Ca(2+) transport, storage and formation of the permeability transition pore is also unknown. This review summarizes studies aimed at identifying these proteins, and describes the properties of a known mitochondrial protein that may be involved in Ca(2+) transport and the structure of the permeability transition pore. | ||
|keywords=Brain mitochondria, Ca2+ accumulation, Ca2+ and Pi precipitate, Calciphorin, Calcium uniporter, Calvectin, Dense granules, gC1qR, Liver mitochondria, Permeability transition pore | |||
}} | }} | ||
{{Labeling | {{Labeling | ||
|additional=Review | |additional=Review | ||
}} | }} |
Latest revision as of 13:01, 19 March 2015
Starkov AA (2010) The molecular identity of the mitochondrial Ca2+ sequestration system. FEBS J. 277:3652-63. |
Starkov AA (2010) FEBS J
Abstract: There is ample evidence to suggest that a dramatic decrease in mitochondrial Ca(2+) retention may contribute to the cell death associated with stroke, excitotoxicity, ischemia and reperfusion, and neurodegenerative diseases. Mitochondria from all studied tissues can accumulate and store Ca(2+) , but the maximum Ca(2+) storage capacity varies widely and exhibits striking tissue specificity. There is currently no explanation for this fact. Precipitation of Ca(2+) and phosphate in the mitochondrial matrix has been suggested to be the major form of storage of accumulated Ca(2+) in mitochondria. How this precipitate is formed is not known. The molecular identity of almost all proteins involved in Ca(2+) transport, storage and formation of the permeability transition pore is also unknown. This review summarizes studies aimed at identifying these proteins, and describes the properties of a known mitochondrial protein that may be involved in Ca(2+) transport and the structure of the permeability transition pore. โข Keywords: Brain mitochondria, Ca2+ accumulation, Ca2+ and Pi precipitate, Calciphorin, Calcium uniporter, Calvectin, Dense granules, gC1qR, Liver mitochondria, Permeability transition pore
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