The complexity of cardiolipin in health and disease

被引:267
作者
Claypool, Steven M. [1 ]
Koehler, Carla M. [2 ,3 ]
机构
[1] Johns Hopkins Sch Med, Dept Physiol, Baltimore, MD 21205 USA
[2] Univ Calif Los Angeles, Inst Mol Biol, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
基金
美国国家卫生研究院;
关键词
BARTH-SYNDROME; INNER MEMBRANE; MITOCHONDRIAL CARDIOLIPIN; TRIFUNCTIONAL PROTEIN; LIVER MITOCHONDRIA; SHOTGUN LIPIDOMICS; OXIDATIVE STRESS; GENETIC ABLATION; ATP SYNTHASE; BIOSYNTHESIS;
D O I
10.1016/j.tibs.2011.09.003
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
Cardiolipin, the signature phospholipid of mitochondria, is a lipid dimer that is important for a diverse range of mitochondrial activities beyond the process of ATP production. Thus not surprisingly, derangements in cardiolipin metabolism are now appreciated to contribute to an assortment of pathological conditions. A comprehensive inventory of enzymes involved in cardiolipin biosynthesis and remodeling was just recently obtained. Post-biosynthesis, the acyl chain composition of cardiolipin is modified by up to three distinct remodeling enzymes that produce either a homogeneous tissue-specific mature form of cardiolipin or alternatively 'bad' cardiolipin that has been linked to mitochondria! dysfunction. In this review, we initially focus on the newly identified players in cardiolipin metabolism and then shift our attention to how changes in cardiolipin metabolism contribute to human disease.
引用
收藏
页码:32 / 41
页数:10
相关论文
共 79 条
[1]   Comparison of lymphoblast mitochondria from normal subjects and patients with Barth syndrome using electron microscopic tomography [J].
Acehan, Devrim ;
Xu, Yang ;
Stokes, David L. ;
Schlame, Michael .
LABORATORY INVESTIGATION, 2007, 87 (01) :40-48
[2]   Cardiolipin Affects the Supramolecular Organization of ATP Synthase in Mitochondria [J].
Acehan, Devrim ;
Malhotra, Ashim ;
Xu, Yang ;
Ren, Mindong ;
Stokes, David L. ;
Schlame, Michael .
BIOPHYSICAL JOURNAL, 2011, 100 (09) :2184-2192
[3]   Cardiac and Skeletal Muscle Defects in a Mouse Model of Human Barth Syndrome [J].
Acehan, Devrim ;
Vaz, Frederic ;
Houtkooper, Riekelt H. ;
James, Jeanne ;
Moore, Vicky ;
Tokunaga, Chonan ;
Kulik, Willem ;
Wansapura, Janaka ;
Toth, Matthew J. ;
Strauss, Arnold ;
Khuchua, Zaza .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (02) :899-908
[4]   Distinct effects of tafazzin deletion in differentiated and undifferentiated mitochondria [J].
Acehan, Devrim ;
Khuchua, Zaza ;
Houtkooper, Riekelt H. ;
Malhotra, Ashim ;
Kaufman, Johanna ;
Vaz, Frederic M. ;
Ren, Mindong ;
Rockman, Howard A. ;
Stokes, David L. ;
Schlame, Michael .
MITOCHONDRION, 2009, 9 (02) :86-95
[5]   OPA1 disease alleles causing dominant optic atrophy have defects in cardiolipin-stimulated GTP hydrolysis and membrane tubulation [J].
Ban, Tadato ;
Heymann, Juergen A. W. ;
Song, Zhiyin ;
Hinshaw, Jenny E. ;
Chan, David C. .
HUMAN MOLECULAR GENETICS, 2010, 19 (11) :2113-2122
[6]   Identification of a Cardiolipin-specific Phospholipase Encoded by the Gene CLD1 (YGR110W) in Yeast [J].
Beranek, Andreas ;
Rechberger, Gerald ;
Knauer, Heide ;
Wolinski, Heimo ;
Kohlwein, Sepp D. ;
Leber, Regina .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (17) :11572-11578
[7]   2 ALPHA-SUBUNIT DONOR SPLICE-SITE MUTATIONS CAUSE HUMAN TRIFUNCTIONAL PROTEIN-DEFICIENCY [J].
BRACKETT, JC ;
SIMS, HF ;
RINALDO, P ;
SHAPIRO, S ;
POWELL, CK ;
BENNETT, MJ ;
STRAUSS, AW .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (05) :2076-2082
[8]   Taz1, an outer mitochondrial membrane protein, affects stability and assembly of inner membrane protein complexes: Implications for Barth syndrome [J].
Brandner, K ;
Mick, DU ;
Frazier, AE ;
Taylor, RD ;
Meisinger, C ;
Rehling, P .
MOLECULAR BIOLOGY OF THE CELL, 2005, 16 (11) :5202-5214
[9]   ALCAT1 is a polyglycerophospholipid acyltransferase potently regulated by adenine nucleotide and thyroid status [J].
Cao, Jingsong ;
Shen, Weiqun ;
Chang, Zhijie ;
Shi, Yuguang .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2009, 296 (04) :E647-E653
[10]   A novel cardiolipin-remodeling pathway revealed by a gene encoding an endoplasmic reticulum-associated acyl-CoA:lysocardiolipin acyltransferase (ALCAT1) in mouse [J].
Cao, JS ;
Liu, YF ;
Lockwood, J ;
Burn, P ;
Shi, YG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (30) :31727-31734