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线粒体心磷脂在心脏功能中的作用及其在心源性疾病中的意义。

The role of mitochondrial cardiolipin in heart function and its implication in cardiac disease.

机构信息

Institute of Cellular Biochemistry, University Medical Center Göttingen, D-37073 Göttingen, Germany.

Institute of Cellular Biochemistry, University Medical Center Göttingen, D-37073 Göttingen, Germany; Max Planck Institute for Biophysical Chemistry, D-37077 Göttingen, Germany.

出版信息

Biochim Biophys Acta Mol Basis Dis. 2019 Apr 1;1865(4):810-821. doi: 10.1016/j.bbadis.2018.08.025. Epub 2018 Aug 26.

Abstract

Mitochondria play an essential role in the energy metabolism of the heart. Many of the essential functions are associated with mitochondrial membranes and oxidative phosphorylation driven by the respiratory chain. Mitochondrial membranes are unique in the cell as they contain the phospholipid cardiolipin. The important role of cardiolipin in cardiovascular health is highlighted by several cardiac diseases, in which cardiolipin plays a fundamental role. Barth syndrome, Sengers syndrome, and Dilated cardiomyopathy with ataxia (DCMA) are genetic disorders, which affect cardiolipin biosynthesis. Other cardiovascular diseases including ischemia/reperfusion injury and heart failure are also associated with changes in the cardiolipin pool. Here, we summarize molecular functions of cardiolipin in mitochondrial biogenesis and morphology. We highlight the role of cardiolipin for the respiratory chain, metabolite carriers, and mitochondrial metabolism and describe links to apoptosis and mitochondria specific autophagy (mitophagy) with possible implications in cardiac disease.

摘要

线粒体在心脏的能量代谢中起着至关重要的作用。许多基本功能与线粒体膜和由呼吸链驱动的氧化磷酸化有关。线粒体膜在细胞中是独一无二的,因为它们含有磷脂心磷脂。几种心脏病突出了心磷脂在心血管健康中的重要作用,其中心磷脂起着根本作用。Barth 综合征、Sengers 综合征和共济失调扩张型心肌病(DCMA)是影响心磷脂生物合成的遗传疾病。其他心血管疾病,包括缺血/再灌注损伤和心力衰竭,也与心磷脂池的变化有关。在这里,我们总结了心磷脂在线粒体生物发生和形态中的分子功能。我们强调了心磷脂对呼吸链、代谢物载体和线粒体代谢的作用,并描述了与细胞凋亡和线粒体特异性自噬(mitophagy)的联系,这可能对心脏病有影响。

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