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活性氧代谢产物增加内皮细胞中的线粒体钙:Ca2+/Na+交换体的作用

Reactive oxygen metabolites increase mitochondrial calcium in endothelial cells: implication of the Ca2+/Na+ exchanger.

作者信息

Jornot L, Maechler P, Wollheim C B, Junod A F

机构信息

Respiratory Division and Division of Clinical Biochemistry, Department of Internal Medicine, University Hospital, Switzerland.

出版信息

J Cell Sci. 1999 Apr;112 ( Pt 7):1013-22. doi: 10.1242/jcs.112.7.1013.

Abstract

In endothelial cells, a bolus of hydrogen peroxide (H2O2) or oxygen metabolites generated by hypoxanthine-xanthine oxidase (HX-XO) increased the mitochondrial calcium concentration [Ca2+]m. Both agents caused a biphasic increase in [Ca2+]m which was preceded by a rise in cytosolic free calcium concentration [Ca2+]c (18 and 6 seconds for H2O2 and HX-XO, respectively). The peak and plateau elevations of [Ca2+] were consistently higher in the mitochondrial matrix than in the cytosol. In Ca2+-free/EGTA medium, the plateau phase of elevated [Ca2+] evoked by H2O2 due to capacitative Ca2+ influx was abolished in the cytosol, but was maintained in the mitochondria. In contrast to H2O2 and HX-XO, ATP which binds the P2Y purinoceptors induced an increase in [Ca2+]m that was similar to that of [Ca2+]c. When cells were first stimulated with inositol 1,4, 5-trisphosphate-generating agonists or the Ca2+-ATPase inhibitor cyclopiazonic acid (CPA), subsequent addition of H2O2 did not affect [Ca2+]c, but still caused an elevation of [Ca2+]m. Moreover, the specific inhibitor of the mitochondrial Ca2+/Na+ exchanger, 7-chloro-3,5-dihydro-5-phenyl-1H-4.1-benzothiazepine-2-on (CGP37157), did not potentiate the effects of H2O2 and HX-XO on [Ca2+]m, while causing a marked increase in the peak [Ca2+]m and a significant attenuation of the rate of [Ca2+]m efflux upon addition of histamine or CPA. In permeabilized cells, H2O2 mimicked the effects of CGP37157 causing an increase in the basal level of matrix free Ca2+ and decreased efflux. Dissipation of the electrochemical proton gradient by carbonylcyanide p-(trifluoromethoxy) phenylhydrazone (FCCP), and blocade of the Ca2+ uptake by ruthenium red prevented [Ca2+]m increases evoked by H2O2. These results demonstrate that the H2O2-induced elevation in [Ca2+]m results from a transfer of Ca2+ secondary to increased [Ca2+]c, and an inhibition of the Ca2+/Na+ electroneutral exchanger of the mitochondria.

摘要

在内皮细胞中,次黄嘌呤 - 黄嘌呤氧化酶(HX - XO)产生的过氧化氢(H₂O₂)或氧代谢产物团块会增加线粒体钙浓度[Ca²⁺]m。这两种物质都会使[Ca²⁺]m呈现双相增加,且在此之前胞质游离钙浓度[Ca²⁺]c会升高(H₂O₂和HX - XO分别为18秒和6秒)。[Ca²⁺]的峰值和平台期升高在线粒体基质中始终高于胞质。在无钙/乙二醇双乙酸盐(EGTA)培养基中,由H₂O₂引发的因钙库调控性钙内流导致的[Ca²⁺]升高的平台期在胞质中消失,但在线粒体中得以维持。与H₂O₂和HX - XO不同,结合P2Y嘌呤受体的ATP会使[Ca²⁺]m增加,且与[Ca²⁺]c的增加相似。当细胞先用产生肌醇1,4,5 - 三磷酸的激动剂或钙 - ATP酶抑制剂环匹阿尼酸(CPA)刺激后,随后添加H₂O₂不会影响[Ca²⁺]c,但仍会使[Ca²⁺]m升高。此外,线粒体钙/钠交换体的特异性抑制剂7 - 氯 - 3,5 - 二氢 - 5 - 苯基 - 1H - 4,1 - 苯并硫氮杂䓬 - 2 - 酮(CGP37157)不会增强H₂O₂和HX - XO对[Ca²⁺]m的作用,而在添加组胺或CPA时会使[Ca²⁺]m的峰值显著增加,并使[Ca²⁺]m外流速率明显降低。在通透细胞中,H₂O₂模拟了CGP37157的作用,导致基质游离钙的基础水平增加并减少外流。羰基氰化物对 - (三氟甲氧基)苯腙(FCCP)使电化学质子梯度消散,以及钌红阻断钙摄取,均能阻止H₂O₂引发的[Ca²⁺]m增加。这些结果表明,H₂O₂诱导的[Ca²⁺]m升高是由于[Ca²⁺]c增加继发的钙转移以及线粒体钙/钠电中性交换体受到抑制所致。

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