Physiological and pathological roles of mitochondrial SLC25 carriers

被引:95
作者
Gutierrez-Aguilar, Manuel [1 ]
Baines, Christopher P. [1 ,2 ,3 ]
机构
[1] Univ Missouri, Dalton Cardiovasc Res Ctr, Columbia, MO 65211 USA
[2] Univ Missouri, Dept Biomed Sci, Columbia, MO 65211 USA
[3] Univ Missouri, Dept Med Pharmacol & Physiol, Columbia, MO 65211 USA
基金
美国国家卫生研究院;
关键词
disease; mitochondrion; solute carrier family 25 (SLC25); transport; RAT-LIVER MITOCHONDRIA; GENOME-WIDE ASSOCIATION; HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME; CONGENITAL SIDEROBLASTIC ANEMIA; PYRIMIDINE NUCLEOTIDE CARRIER; STIMULATED INSULIN-SECRETION; TISSUE-SPECIFIC EXPRESSION; BEEF-HEART MITOCHONDRIA; BROWN FAT MITOCHONDRIA; BETA-CELL DYSFUNCTION;
D O I
10.1042/BJ20121753
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The mitochondrion relies on compartmentalization of certain enzymes, ions and metabolites for the sake of efficient metabolism. In order to fulfil its activities, a myriad of carriers are properly expressed, targeted and folded in the inner mitochondrial membrane. Among these carriers, the six-transmembrane-helix mitochondrial SLC25 (solute carrier family 25) proteins facilitate transport of solutes with disparate chemical identities across the inner mitochondrial membrane. Although their proper function replenishes building blocks needed for metabolic reactions, dysfunctional SLC25 proteins are involved in pathological states. It is the purpose of the present review to cover the current knowledge on the role of SLC25 transporters in health and disease.
引用
收藏
页码:371 / 386
页数:16
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