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2
Spontaneous intermembrane transfer of various cholesterol-derived hydroperoxide species: kinetic studies with model membranes and cells.各种胆固醇衍生的氢过氧化物的自发膜间转移:模型膜和细胞的动力学研究
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3
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本文引用的文献

1
Cholesterol Hydroperoxide Generation, Translocation, and Reductive Turnover in Biological Systems.生物系统中胆固醇过氧化氢的生成、转运及还原代谢
Cell Biochem Biophys. 2017 Dec;75(3-4):413-419. doi: 10.1007/s12013-017-0799-0. Epub 2017 Apr 22.
2
Intracellular cholesterol transport proteins: roles in health and disease.细胞内胆固醇转运蛋白:在健康与疾病中的作用
Clin Sci (Lond). 2016 Nov 1;130(21):1843-59. doi: 10.1042/CS20160339.
3
Cholesterol as a natural probe for free radical-mediated lipid peroxidation in biological membranes and lipoproteins.胆固醇作为生物膜和脂蛋白中自由基介导的脂质过氧化的天然探针。
J Chromatogr B Analyt Technol Biomed Life Sci. 2016 Apr 15;1019:202-9. doi: 10.1016/j.jchromb.2015.12.034. Epub 2015 Dec 28.
4
Reversible oxidation of phosphatase and tensin homolog (PTEN) alters its interactions with signaling and regulatory proteins.磷酸酶和张力蛋白同源物(PTEN)的可逆氧化会改变其与信号转导和调节蛋白的相互作用。
Free Radic Biol Med. 2016 Jan;90:24-34. doi: 10.1016/j.freeradbiomed.2015.11.004. Epub 2015 Nov 10.
5
Mitochondrial regulation of macrophage cholesterol homeostasis.线粒体对巨噬细胞胆固醇稳态的调节。
Free Radic Biol Med. 2015 Dec;89:982-92. doi: 10.1016/j.freeradbiomed.2015.08.010. Epub 2015 Sep 28.
6
Impairment of Macrophage Cholesterol Efflux by Cholesterol Hydroperoxide Trafficking: Implications for Atherogenesis Under Oxidative Stress.胆固醇氢过氧化物转运导致巨噬细胞胆固醇流出受损:对氧化应激下动脉粥样硬化形成的影响。
Arterioscler Thromb Vasc Biol. 2015 Oct;35(10):2104-13. doi: 10.1161/ATVBAHA.115.306210. Epub 2015 Aug 27.
7
Cholesterol under oxidative stress-How lipid membranes sense oxidation as cholesterol is being replaced by oxysterols.氧化应激下的胆固醇——脂质膜如何感知胆固醇被氧化固醇取代。
Free Radic Biol Med. 2015 Jul;84:30-41. doi: 10.1016/j.freeradbiomed.2015.03.006. Epub 2015 Mar 17.
8
Macrophage mitochondrial damage from StAR transport of 7-hydroperoxycholesterol: implications for oxidative stress-impaired reverse cholesterol transport.StAR 转运 7-羟胆固醇导致巨噬细胞线粒体损伤:对氧化应激损伤胆固醇逆转运的启示。
FEBS Lett. 2014 Jan 3;588(1):65-70. doi: 10.1016/j.febslet.2013.10.051. Epub 2013 Nov 21.
9
Deleterious cholesterol hydroperoxide trafficking in steroidogenic acute regulatory (StAR) protein-expressing MA-10 Leydig cells: implications for oxidative stress-impaired steroidogenesis.甾醇生成急性调节蛋白(StAR)蛋白表达的 MA-10 莱迪希细胞中有害胆固醇氢过氧化物的转运:对氧化应激损害类固醇生成的影响。
J Biol Chem. 2013 Apr 19;288(16):11509-19. doi: 10.1074/jbc.M113.452151. Epub 2013 Mar 6.
10
Pathways of cholesterol oxidation via non-enzymatic mechanisms.胆固醇非酶氧化途径。
Chem Phys Lipids. 2011 Sep;164(6):457-68. doi: 10.1016/j.chemphyslip.2011.06.006. Epub 2011 Jun 15.

胆固醇过氧化作用作为光动力体系中一种特殊类型的脂质过氧化作用。

Cholesterol Peroxidation as a Special Type of Lipid Oxidation in Photodynamic Systems.

机构信息

Department of Biochemistry, Medical College of Wisconsin, Milwaukee, WI.

Department of Biophysics, Jagiellonian University, Krakow, Poland.

出版信息

Photochem Photobiol. 2019 Jan;95(1):73-82. doi: 10.1111/php.12969. Epub 2018 Aug 2.

DOI:10.1111/php.12969
PMID:29962109
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6312749/
Abstract

Like other unsaturated lipids in cell membranes and lipoproteins, cholesterol (Ch) is susceptible to oxidative modification, including photodynamic oxidation. There is a sustained interest in the pathogenic properties of Ch oxides such as those generated by photooxidation. Singlet oxygen ( O )-mediated Ch photooxidation (Type II mechanism) gives rise to three hydroperoxide (ChOOH) isomers: 5α-OOH, 6α-OOH and 6β-OOH, the 5α-OOH yield far exceeding that of the others. 5α-OOH detection is relatively straightforward and serves as a definitive indicator of O involvement in a reaction, photochemical or otherwise. Like all lipid hydroperoxides (LOOHs), ChOOHs can disrupt membrane or lipoprotein structure/function on their own, but subsequent light-independent reactions may either intensify or attenuate such effects. Such reactions include (1) one-electron reduction to redox-active free radical intermediates, (2) two-electron reduction to redox-silent alcohols and (3) translocation to other lipid compartments, where (1) or (2) may take place. In addition to these effects, ChOOHs may act as signaling molecules in reactions that affect cell fates. Although processes a-c have been well studied for ChOOHs, signaling activity is still poorly understood compared with that of hydrogen peroxide. This review focuses on these various aspects Ch photoperoxidation and its biological consequences.

摘要

与细胞膜和脂蛋白中的其他不饱和脂质一样,胆固醇 (Ch) 容易发生氧化修饰,包括光动力学氧化。Ch 氧化物(如光氧化产生的氧化物)的致病特性一直是人们关注的焦点。单线态氧 ( O )介导的 Ch 光氧化(II 型机制)产生三种氢过氧化物(ChOOH)异构体:5α-OOH、6α-OOH 和 6β-OOH,5α-OOH 的产率远远超过其他两种。5α-OOH 的检测相对简单,是 O 参与反应(光化学或其他反应)的明确指标。与所有脂质氢过氧化物 (LOOH) 一样,ChOOH 本身可以破坏膜或脂蛋白的结构/功能,但随后的非光依赖性反应可能会增强或减弱这种效应。此类反应包括 (1) 单电子还原为氧化还原活性自由基中间体,(2) 双电子还原为氧化还原沉默醇,以及 (3) 转移到其他脂质隔室,其中 (1) 或 (2) 可能发生。除了这些影响外,ChOOH 还可以作为影响细胞命运的反应中的信号分子。尽管 ChOOH 的过程 a-c 已经得到了很好的研究,但与过氧化氢相比,其信号活性仍知之甚少。这篇综述重点介绍了 Ch 光氧化及其生物学后果的各个方面。