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线粒体心磷脂的生物合成、重塑和周转。

Biosynthesis, remodeling and turnover of mitochondrial cardiolipin.

机构信息

Department of Anesthesiology and Cell Biology, New York University School of Medicine, New York, NY 10016, USA.

Department of Biological Sciences, Wayne State University, Detroit, MI 48202, USA.

出版信息

Biochim Biophys Acta Mol Cell Biol Lipids. 2017 Jan;1862(1):3-7. doi: 10.1016/j.bbalip.2016.08.010. Epub 2016 Aug 21.

DOI:10.1016/j.bbalip.2016.08.010
PMID:27556952
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5125896/
Abstract

Among mitochondrial lipids, cardiolipin occupies a unique place. It is the only phospholipid that is specific to mitochondria and although it is merely a minor component, accounting for 10-20% of the total phospholipid content, cardiolipin plays an important role in the molecular organization, and thus the function of the cristae. This review covers the formation of cardiolipin, a phospholipid dimer containing two phosphatidyl residues, and its assembly into mitochondrial membranes. While a large body of literature exists on this topic, the review focuses on papers that appeared in the past three years. This article is part of a Special Issue entitled: Lipids of Mitochondria edited by Guenther Daum.

摘要

在线粒体脂质中,心磷脂占据着独特的地位。它是唯一一种特异存在于线粒体的磷脂,虽然它仅占总磷脂含量的 10-20%,但在心磷脂在嵴的分子组织和功能中起着重要作用。本篇综述涵盖了心磷脂的形成,心磷脂是一种含有两个磷脂酰基的磷脂二聚体,以及它在 线粒体膜中的组装。虽然关于这个主题已经有大量的文献,但这篇综述重点关注了过去三年发表的论文。本文是由 Guenther Daum 编辑的题为“线粒体的脂质”特刊的一部分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0be3/5125896/305551e228dc/nihms812078f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0be3/5125896/305551e228dc/nihms812078f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0be3/5125896/305551e228dc/nihms812078f1.jpg

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本文引用的文献

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Loss of protein association causes cardiolipin degradation in Barth syndrome.蛋白质结合的丧失导致巴氏综合征中的心磷脂降解。
Nat Chem Biol. 2016 Aug;12(8):641-7. doi: 10.1038/nchembio.2113. Epub 2016 Jun 27.
2
Mechanism for Remodeling of the Acyl Chain Composition of Cardiolipin Catalyzed by Saccharomyces cerevisiae Tafazzin.酿酒酵母塔法辛催化的心磷脂酰基链组成重塑机制。
J Biol Chem. 2016 Jul 22;291(30):15491-502. doi: 10.1074/jbc.M116.718510. Epub 2016 Jun 6.
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Defining functional classes of Barth syndrome mutation in humans.定义人类巴氏综合征突变的功能类别。
Hum Mol Genet. 2016 May 1;25(9):1754-70. doi: 10.1093/hmg/ddw046. Epub 2016 Feb 16.
4
NDPK-D (NM23-H4)-mediated externalization of cardiolipin enables elimination of depolarized mitochondria by mitophagy.NDPK-D(NM23-H4)介导的心磷脂外化能够通过线粒体自噬消除去极化的线粒体。
Cell Death Differ. 2016 Jul;23(7):1140-51. doi: 10.1038/cdd.2015.160. Epub 2016 Jan 8.
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Cardiac-specific succinate dehydrogenase deficiency in Barth syndrome.心肌特异性琥珀酸脱氢酶缺乏症与 Barth 综合征。
EMBO Mol Med. 2016 Feb 1;8(2):139-54. doi: 10.15252/emmm.201505644.
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Interaction of MDM33 with mitochondrial inner membrane homeostasis pathways in yeast.酵母中MDM33与线粒体内膜稳态途径的相互作用。
Sci Rep. 2015 Dec 16;5:18344. doi: 10.1038/srep18344.
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