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线粒体中胞质钙振荡的解码

Decoding of cytosolic calcium oscillations in the mitochondria.

作者信息

Hajnóczky G, Robb-Gaspers L D, Seitz M B, Thomas A P

机构信息

Department of Pathology, Anatomy and Cell Biology, Thomas Jefferson University, Philadelphia, Pennsylvania 19107, USA.

出版信息

Cell. 1995 Aug 11;82(3):415-24. doi: 10.1016/0092-8674(95)90430-1.

Abstract

Frequency-modulated oscillations of cytosolic Ca2+ ([Ca2+]c) are believed to be important in signal transduction, but it has been difficult to correlate [Ca2+]c oscillations directly with the activity of Ca(2+)-regulated targets. We have studied the control of Ca(2+)-sensitive mitochondrial dehydrogenases (CSMDHs) by monitoring mitochondrial Ca2+ ([Ca2+]m) and the redox state of flavoproteins and pyridine nucleotides simultaneously with [Ca2+]c in single hepatocytes. Oscillations of [Ca2+]c induced by IP3-dependent hormones were efficiently transmitted to the mitochondria as [Ca2+]m oscillations. Each [Ca2+]m spike was sufficient to cause a maximal transient activation of the CSMDHs and [Ca2+]m oscillations at frequencies above 0.5 per minute caused a sustained activation of mitochondrial metabolism. By contrast, sustained [Ca2+]c increases yielded only transient CSMDH activation, and slow or partial [Ca2+]c elevations were ineffective in increasing [Ca2+]m or stimulating CSMDHs. We conclude that the mitochondria are tuned to oscillating [Ca2+]c signals, the frequency of which can control the CSMDHs over the full range of potential activities.

摘要

胞质Ca2+([Ca2+]c)的调频振荡被认为在信号转导中很重要,但一直难以将[Ca2+]c振荡与Ca(2+)调节靶点的活性直接关联起来。我们通过在单个肝细胞中同时监测线粒体Ca2+([Ca2+]m)以及黄素蛋白和吡啶核苷酸的氧化还原状态与[Ca2+]c,研究了Ca(2+)敏感的线粒体脱氢酶(CSMDHs)的调控。由IP3依赖性激素诱导的[Ca2+]c振荡作为[Ca2+]m振荡有效地传递到线粒体。每个[Ca2+]m峰值足以引起CSMDHs的最大瞬时激活,并且每分钟频率高于0.5的[Ca2+]m振荡会导致线粒体代谢的持续激活。相比之下,[Ca2+]c的持续增加仅产生瞬时的CSMDH激活,而缓慢或部分的[Ca2+]c升高在增加[Ca2+]m或刺激CSMDHs方面无效。我们得出结论,线粒体能够适应振荡的[Ca2+]c信号,其频率可以在潜在活性的整个范围内控制CSMDHs。

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