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线粒体内膜中一种非特异性孔道的钙依赖性开放在pH值低于7时受到抑制。这对低pH值对化学和缺氧性细胞损伤的保护作用具有启示意义。

Calcium-dependent opening of a non-specific pore in the mitochondrial inner membrane is inhibited at pH values below 7. Implications for the protective effect of low pH against chemical and hypoxic cell damage.

作者信息

Halestrap A P

机构信息

Department of Biochemistry, School of Medical Sciences, University of Bristol, U.K.

出版信息

Biochem J. 1991 Sep 15;278 ( Pt 3)(Pt 3):715-9. doi: 10.1042/bj2780715.

DOI:10.1042/bj2780715
PMID:1654889
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1151405/
Abstract
  1. The rate of opening of the Ca(2+)-induced non-specific, cyclosporin A-inhibited, pore of the mitochondrial inner membrane of rat heart and liver mitochondria at pH 6.0 was less than 10% of that at pH 7.4. 2. The effect could not be explained by inhibition of Ca2+ uptake into the mitochondria, or of the matrix peptidyl-prolyl cis-trans isomerase (PPIase), or of the Ca(2+)-induced conformational change of the adenine nucleotide translocase. 3. It is suggested that the proposed interaction of matrix PPIase with the 'c' conformation of the adenine nucleotide carrier in the presence of Ca2+ [Griffiths & Halestrap (1991) Biochem. J. 274, 611-614] is inhibited by low pH. 4. The relevance of this to the protective effect of low pH on hypoxic and chemical-induced cell damage is discussed.
摘要
  1. 在pH 6.0时,大鼠心脏和肝脏线粒体线粒体内膜上钙诱导的、环孢素A抑制的非特异性孔道的开放速率不到pH 7.4时的10%。2. 这种效应无法通过抑制钙离子摄入线粒体、基质肽基脯氨酰顺反异构酶(PPIase)或钙诱导的腺嘌呤核苷酸转位酶构象变化来解释。3. 有人提出,在钙离子存在的情况下,基质PPIase与腺嘌呤核苷酸载体的“c”构象之间的相互作用[Griffiths & Halestrap (1991) Biochem. J. 274, 611 - 614]会受到低pH的抑制。4. 文中讨论了这与低pH对缺氧和化学诱导的细胞损伤的保护作用的相关性。

相似文献

1
Calcium-dependent opening of a non-specific pore in the mitochondrial inner membrane is inhibited at pH values below 7. Implications for the protective effect of low pH against chemical and hypoxic cell damage.线粒体内膜中一种非特异性孔道的钙依赖性开放在pH值低于7时受到抑制。这对低pH值对化学和缺氧性细胞损伤的保护作用具有启示意义。
Biochem J. 1991 Sep 15;278 ( Pt 3)(Pt 3):715-9. doi: 10.1042/bj2780715.
2
Inhibition of Ca2(+)-induced large-amplitude swelling of liver and heart mitochondria by cyclosporin is probably caused by the inhibitor binding to mitochondrial-matrix peptidyl-prolyl cis-trans isomerase and preventing it interacting with the adenine nucleotide translocase.环孢素抑制Ca2+诱导的肝脏和心脏线粒体大幅度肿胀,可能是由于该抑制剂与线粒体基质肽基脯氨酰顺反异构酶结合,阻止其与腺嘌呤核苷酸转位酶相互作用所致。
Biochem J. 1990 May 15;268(1):153-60. doi: 10.1042/bj2680153.
3
Further evidence that cyclosporin A protects mitochondria from calcium overload by inhibiting a matrix peptidyl-prolyl cis-trans isomerase. Implications for the immunosuppressive and toxic effects of cyclosporin.环孢菌素A通过抑制一种基质肽基脯氨酰顺反异构酶来保护线粒体免受钙超载的进一步证据。对环孢菌素免疫抑制和毒性作用的启示。
Biochem J. 1991 Mar 1;274 ( Pt 2)(Pt 2):611-4. doi: 10.1042/bj2740611.
4
Chaotropic agents and increased matrix volume enhance binding of mitochondrial cyclophilin to the inner mitochondrial membrane and sensitize the mitochondrial permeability transition to [Ca2+].促溶剂和增加的基质体积增强线粒体亲环蛋白与线粒体内膜的结合,并使线粒体通透性转换对[Ca2+]敏感。
Biochemistry. 1996 Jun 25;35(25):8172-80. doi: 10.1021/bi9525177.
5
To involvement the conformation of the adenine nucleotide translocase in opening the Tl(+)-induced permeability transition pore in Ca(2+)-loaded rat liver mitochondria.关于腺嘌呤核苷酸转位酶在打开钙离子负载的大鼠肝线粒体中铊(Tl⁺)诱导的通透性转换孔过程中的构象变化。 (注:原英文表述不太准确规范,正常应该是“To investigate the conformation of the adenine nucleotide translocase in the opening of the Tl(+)-induced permeability transition pore in Ca(2+)-loaded rat liver mitochondria.” 翻译为“为了研究腺嘌呤核苷酸转位酶在钙离子负载的大鼠肝线粒体中铊(Tl⁺)诱导的通透性转换孔开放过程中的构象” 这里按照你要求的原英文进行翻译)
Toxicol In Vitro. 2016 Apr;32:320-32. doi: 10.1016/j.tiv.2016.01.015. Epub 2016 Feb 4.
6
Recruitment of mitochondrial cyclophilin to the mitochondrial inner membrane under conditions of oxidative stress that enhance the opening of a calcium-sensitive non-specific channel.在增强钙敏感性非特异性通道开放的氧化应激条件下,线粒体亲环蛋白被招募至线粒体内膜。
Biochem J. 1994 Sep 1;302 ( Pt 2)(Pt 2):321-4. doi: 10.1042/bj3020321.
7
Involvement of cyclophilin D in the activation of a mitochondrial pore by Ca2+ and oxidant stress.亲环蛋白D参与Ca2+和氧化应激激活线粒体孔道的过程。
Eur J Biochem. 1996 May 15;238(1):166-72. doi: 10.1111/j.1432-1033.1996.0166q.x.
8
Liver mitochondrial pyrophosphate concentration is increased by Ca2+ and regulates the intramitochondrial volume and adenine nucleotide content.肝脏线粒体焦磷酸浓度会因钙离子而升高,并调节线粒体内的体积和腺嘌呤核苷酸含量。
Biochem J. 1987 Sep 15;246(3):715-23. doi: 10.1042/bj2460715.
9
The presence of two classes of high-affinity cyclosporin A binding sites in mitochondria. Evidence that the minor component is involved in the opening of an inner-membrane Ca(2+)-dependent pore.线粒体中存在两类高亲和力的环孢菌素A结合位点。有证据表明次要成分参与内膜钙依赖性孔道的开放。
Eur J Biochem. 1990 Dec 12;194(2):671-9. doi: 10.1111/j.1432-1033.1990.tb15667.x.
10
Evidence for the involvement of a membrane-associated cyclosporin-A-binding protein in the Ca(2+)-activated inner membrane pore of heart mitochondria.有证据表明,一种与膜相关的环孢菌素A结合蛋白参与了心脏线粒体Ca(2+)激活的内膜孔道。
Eur J Biochem. 1995 Jun 15;230(3):1125-32. doi: 10.1111/j.1432-1033.1995.tb20664.x.

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Myocardial ischemia: the pathogenesis of irreversible cell injury in ischemia.心肌缺血:缺血性不可逆细胞损伤的发病机制。
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Beneficial effect of cyclosporine pretreatment in preventing ischemic damage to the liver in dogs.环孢素预处理对预防犬肝脏缺血性损伤的有益作用。
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10
Inhibition by cyclosporin A of a Ca2+-dependent pore in heart mitochondria activated by inorganic phosphate and oxidative stress.环孢菌素A对无机磷酸盐和氧化应激激活的心脏线粒体中钙依赖性孔道的抑制作用。
Biochem J. 1988 Oct 1;255(1):357-60.