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亲环素 D 的生理功能和线粒体通透性转换孔。

Physiologic functions of cyclophilin D and the mitochondrial permeability transition pore.

机构信息

Center for Translational Medicine, Department of Pharmacology, Temple University School of Medicine, Philadelphia, PA 19140, USA.

出版信息

Circ J. 2013;77(5):1111-22. doi: 10.1253/circj.cj-13-0321. Epub 2013 Mar 29.

DOI:10.1253/circj.cj-13-0321
PMID:23538482
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6397958/
Abstract

This review focuses on the role of cyclophilin D (CypD) as a prominent mediator of the mitochondrial permeability transition pore (MPTP) and subsequent effects on cardiovascular physiology and pathology. Although a great number of reviews have been written on the MPTP and its effects on cell death, we focus on the biology surrounding CypD itself and the non-cell death physiologic functions of the MPTP. A greater understanding of the physiologic functions of the MPTP and its regulation by CypD will likely suggest novel therapeutic approaches for cardiovascular disease, both dependent and independent of programmed necrotic cell death mechanisms.

摘要

这篇综述重点探讨了亲环素 D(CypD)作为线粒体通透性转换孔(MPTP)的主要介质的作用,以及其对心血管生理学和病理学的后续影响。尽管已经有大量关于 MPTP 及其对细胞死亡影响的综述文章,但我们重点关注 CypD 本身的生物学特性以及 MPTP 的非细胞死亡生理功能。更好地了解 MPTP 的生理功能及其受 CypD 调控的机制,可能会为依赖和不依赖程序性坏死细胞死亡机制的心血管疾病提供新的治疗方法。

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本文引用的文献

1
Role of the c subunit of the FO ATP synthase in mitochondrial permeability transition.FO ATP 合酶 C 亚基在线粒体通透性转换中的作用。
Cell Cycle. 2013 Feb 15;12(4):674-83. doi: 10.4161/cc.23599. Epub 2013 Jan 23.
2
The mitochondrial transporter family SLC25: identification, properties and physiopathology.线粒体转运蛋白家族 SLC25:鉴定、特性和病理生理学。
Mol Aspects Med. 2013 Apr-Jun;34(2-3):465-84. doi: 10.1016/j.mam.2012.05.005. Epub 2012 Dec 23.
3
CypD(-/-) hearts have altered levels of proteins involved in Krebs cycle, branch chain amino acid degradation and pyruvate metabolism.CypD(-/-) 心脏中的蛋白水平发生改变,这些蛋白涉及三羧酸循环、支链氨基酸降解和丙酮酸代谢。
J Mol Cell Cardiol. 2013 Mar;56:81-90. doi: 10.1016/j.yjmcc.2012.12.004. Epub 2012 Dec 19.
4
Cyclophilin inhibitors: an emerging class of therapeutics for the treatment of chronic hepatitis C infection.亲环素抑制剂:治疗慢性丙型肝炎感染的新兴治疗类别。
Viruses. 2012 Oct 29;4(11):2558-77. doi: 10.3390/v4112558.
5
CDD: conserved domains and protein three-dimensional structure.CDD:保守结构域和蛋白质三维结构。
Nucleic Acids Res. 2013 Jan;41(Database issue):D348-52. doi: 10.1093/nar/gks1243. Epub 2012 Nov 28.
6
MCUR1 is an essential component of mitochondrial Ca2+ uptake that regulates cellular metabolism.MCUR1 是线粒体钙摄取的必需组成部分,可调节细胞代谢。
Nat Cell Biol. 2012 Dec;14(12):1336-43. doi: 10.1038/ncb2622. Epub 2012 Nov 25.
7
Is p53 the long-sought molecular trigger for cyclophilin D-regulated mitochondrial permeability transition pore formation and necrosis?p53是长期以来一直在寻找的亲环蛋白D调节的线粒体通透性转换孔形成和坏死的分子触发因素吗?
Circ Res. 2012 Oct 26;111(10):1258-60. doi: 10.1161/CIRCRESAHA.112.280990.
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Mitochondrial control of cellular life, stress, and death.线粒体对细胞生命、应激和死亡的控制。
Circ Res. 2012 Oct 12;111(9):1198-207. doi: 10.1161/CIRCRESAHA.112.268946.
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p53 opens the mitochondrial permeability transition pore to trigger necrosis.p53 打开线粒体通透性转换孔以引发细胞坏死。
Cell. 2012 Jun 22;149(7):1536-48. doi: 10.1016/j.cell.2012.05.014.
10
Mechanisms of cell death in heart disease.心脏病中细胞死亡的机制。
Arterioscler Thromb Vasc Biol. 2012 Jul;32(7):1552-62. doi: 10.1161/ATVBAHA.111.224915. Epub 2012 May 17.