Suppr超能文献

流式细胞术分析钙诱导的分离大鼠肝线粒体膜通透性转换。

Flow cytometric analysis of ca-induced membrane permeability transition of isolated rat liver mitochondria.

机构信息

Department of Cytology & Histology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, 2-5-1 Shikatacho, Okayama 700-8558, Japan.

出版信息

J Clin Biochem Nutr. 2008 Jan;42(1):35-44. doi: 10.3164/jcbn.2008006.

Abstract

The membrane permeability transition (MPT) of mitochondria plays an important role in the mechanism of apoptotic cell death in various cells. Classic type MPT is induced by Ca(2+) in the presence of inorganic phosphate and respiratory substrate, and is characterized by various events including generation of reactive oxygen species (ROS), membrane depolarization, swelling, release of Ca(2+) and high sensitivity to cyclosporine A. However, the sequence of these events and the effect of antioxidants on their events remain obscure. Flow cytometry is a convenient method to investigate the order of events among various functions occurring in MPT using a limited amount of mitochondria (200 microl of 0.02 mg protein/ml) without contamination by other organelles. Flow cytometric analysis revealed that Ca(2+) sequentially induced ROS generation, depolarization, swelling and Ca(2+) release in mitochondria by a cyclosporine A-inhibitable mechanism. These results were supported by the finding that Ca(2+)-induced MPT was inhibited by antioxidants, such as glutathione and N-acetylcysteine. It was also revealed that various inhibitors of Ca(2+)-induced phospholipase A(2) suppressed all of the events associated with Ca(2+)-induced MPT. These results suggested that ROS generation and phospholipase A(2) activation by Ca(2+) underlie the mechanism of the initiation of MPT.

摘要

线粒体的膜通透性转变(MPT)在各种细胞的细胞凋亡死亡机制中起着重要作用。经典的 MPT 是在存在无机磷酸盐和呼吸底物的情况下由 Ca(2+) 诱导的,其特征是各种事件,包括活性氧(ROS)的产生、膜去极化、肿胀、Ca(2+)的释放以及对环孢菌素 A 的高敏感性。然而,这些事件的顺序以及抗氧化剂对其事件的影响仍然不清楚。流式细胞术是一种方便的方法,可使用有限量的线粒体(200 μl 为 0.02mg 蛋白/ml),无需其他细胞器的污染,研究 MPT 中发生的各种功能之间的事件顺序。流式细胞术分析表明,Ca(2+) 通过环孢菌素 A 抑制机制依次诱导线粒体中 ROS 的产生、去极化、肿胀和 Ca(2+)的释放。抗氧化剂,如谷胱甘肽和 N-乙酰半胱氨酸,抑制 Ca(2+)-诱导的 MPT,这一发现支持了这些结果。还发现 Ca(2+)-诱导的磷脂酶 A(2)的各种抑制剂抑制了与 Ca(2+)-诱导的 MPT 相关的所有事件。这些结果表明,Ca(2+)诱导的 ROS 生成和磷脂酶 A(2)的激活是 MPT 起始机制的基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c85/2212344/5e469da530e2/jcbn2008006f01.jpg

相似文献

8
Contribution of liver mitochondrial membrane-bound glutathione transferase to mitochondrial permeability transition pores.
Toxicol Appl Pharmacol. 2009 Feb 15;235(1):77-85. doi: 10.1016/j.taap.2008.11.016. Epub 2008 Dec 6.

引用本文的文献

1
Induction of mitochondrial dysfunction by poly(ADP-ribose) polymer: implication for neuronal cell death.
Mol Cells. 2013 Sep;36(3):258-66. doi: 10.1007/s10059-013-0172-0. Epub 2013 Aug 29.
2
Characterization of functionally distinct mitochondrial subpopulations.
J Bioenerg Biomembr. 2013 Feb;45(1-2):87-99. doi: 10.1007/s10863-012-9478-4. Epub 2012 Oct 19.
3
Effect of trifluoperazine on toxicity, HIF-1α induction and hepatocyte regeneration in acetaminophen toxicity in mice.
Toxicol Appl Pharmacol. 2012 Oct 15;264(2):192-201. doi: 10.1016/j.taap.2012.08.001. Epub 2012 Aug 10.

本文引用的文献

1
Role of Ca2+-independent phospholipase A2gamma in Ca2+-induced mitochondrial permeability transition.
J Pharmacol Exp Ther. 2007 May;321(2):707-15. doi: 10.1124/jpet.107.119545. Epub 2007 Feb 20.
2
Calcium-dependent spontaneously reversible remodeling of brain mitochondria.
J Biol Chem. 2006 Dec 8;281(49):37547-58. doi: 10.1074/jbc.M607263200. Epub 2006 Oct 19.
3
Selective fluorescent imaging of superoxide in vivo using ethidium-based probes.
Proc Natl Acad Sci U S A. 2006 Oct 10;103(41):15038-43. doi: 10.1073/pnas.0601945103. Epub 2006 Oct 2.
4
Biphasic regulation of mitochondrial Ca2+ uptake by cytosolic Ca2+ concentration.
Curr Biol. 2006 Aug 22;16(16):1672-7. doi: 10.1016/j.cub.2006.06.059.
5
Phospholipase A2, reactive oxygen species, and lipid peroxidation in cerebral ischemia.
Free Radic Biol Med. 2006 Feb 1;40(3):376-87. doi: 10.1016/j.freeradbiomed.2005.08.044. Epub 2005 Nov 21.
7
Mitochondria-targeted peptide prevents mitochondrial depolarization and apoptosis induced by tert-butyl hydroperoxide in neuronal cell lines.
Biochem Pharmacol. 2005 Dec 5;70(12):1796-806. doi: 10.1016/j.bcp.2005.08.022. Epub 2005 Oct 10.
8
Comparative kinetic analysis reveals that inducer-specific ion release precedes the mitochondrial permeability transition.
Biochim Biophys Acta. 2005 Jul 15;1708(3):375-92. doi: 10.1016/j.bbabio.2005.05.009.
9
On the role of the respiratory complex I on membrane permeability transition.
J Bioenerg Biomembr. 2005 Feb;37(1):17-23. doi: 10.1007/s10863-005-4119-9.
10
Reactive oxygen species and the mitochondrial signaling pathway of cell death.
Histol Histopathol. 2005 Jan;20(1):205-19. doi: 10.14670/HH-20.205.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验