Hatch G M
Department of Pharmacology and Therapeutics, University of Manitoba, Winnipeg, Manitoba, R3E OW3, Canada.
Int J Mol Med. 1998 Jan;1(1):33-41. doi: 10.3892/ijmm.1.1.33.
Cardiolipin is the principal polyglycerophospholipid found in the heart and most mammalian tissues. This phospholipid is the only phospholipid localized exclusively to the mitochondria of mammalian cells. Cardiolipin appears to be involved, either directly or indirectly, in the modulation of a number of cellular processes including the activation of mitochondrial enzymes and hence production of energy by oxidative phosphorylation. The regulatory properties which govern cardiolipin biosynthesis, its remodeling and trafficking are beginning to emerge. Studies in the isolated perfused rat heart and H9c2 cardiac myoblast cells have indicated that the rate-limiting step of cardiolipin biosynthesis, via the cytidine-5'-diphosphate-1,2-diacyl-sn-glycerol pathway, is the conversion of phosphatidic acid and cytidine-5'-triphosphate to cytidine-5'-diphosphate-1,2-diacyl-sn-glycerol. The cellular level of cytidine-5'-triphosphate appears to control the production of cardiolipin in H9c2 cells. The activities of the other enzymes of the cytidine-5'-diphosphate-1,2-diacyl-sn-glycerol pathway of cardiolipin biosynthesis in the heart may be modulated by thyroid hormone and unsaturated fatty acids. In addition, extra-mitochondrial cytidine-5'-diphosphate-1,2-diacyl-sn-glycerol and phosphatidylglycerol may be utilized for cardiolipin biosynthesis in the heart and permeabilized cells. Cardiolipin may be readily hydrolyzed by phospholipases and may be remodeled by a deacylation-reacylation pathway. Studies with a Chinese hamster lung fibroblast cell line CCL16-B2 have indicated that the remodeling of cardiolipin is markedly altered in the mitochondria of these cells and that this alteration in remodeling may be one of the underlying mechanisms for the mutation in oxidative energy production in these cells. Host cell cardiolipin may be trafficked from the mitochondria to an intracellular bacterial parasite Chlamydia trachomatis. The purpose of this review is to briefly discuss some of the more recent findings in cardiolipin metabolism in the heart and mammalian cells and to provide insight into their possible implications in the regulation of some cellular functions in mammalian tissues and cells.
心磷脂是在心脏和大多数哺乳动物组织中发现的主要多甘油磷脂。这种磷脂是唯一专门定位于哺乳动物细胞线粒体的磷脂。心磷脂似乎直接或间接地参与了许多细胞过程的调节,包括线粒体酶的激活以及因此通过氧化磷酸化产生能量。控制心磷脂生物合成、重塑和运输的调节特性正逐渐显现出来。对离体灌注大鼠心脏和H9c2心肌成纤维细胞的研究表明,在心磷脂生物合成的胞苷-5'-二磷酸-1,2-二酰基-sn-甘油途径中,限速步骤是磷脂酸和胞苷-5'-三磷酸转化为胞苷-5'-二磷酸-1,2-二酰基-sn-甘油。胞苷-5'-三磷酸的细胞水平似乎控制着H9c2细胞中心磷脂的产生。心脏中心磷脂生物合成的胞苷-5'-二磷酸-1,2-二酰基-sn-甘油途径中其他酶的活性可能受到甲状腺激素和不饱和脂肪酸的调节。此外,线粒体外的胞苷-5'-二磷酸-1,2-二酰基-sn-甘油和磷脂酰甘油可用于心脏和通透细胞的心磷脂生物合成。心磷脂可被磷脂酶轻易水解,并可通过脱酰基-再酰基化途径进行重塑。对中国仓鼠肺成纤维细胞系CCL16-B2的研究表明,这些细胞线粒体中心磷脂的重塑明显改变,而这种重塑改变可能是这些细胞氧化能量产生突变的潜在机制之一。宿主细胞的心磷脂可能从线粒体运输到细胞内细菌寄生虫沙眼衣原体。这篇综述的目的是简要讨论心脏和哺乳动物细胞中心磷脂代谢的一些最新发现,并深入了解它们在调节哺乳动物组织和细胞某些细胞功能方面的可能意义。