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肌醇1,4,5-三磷酸介导的Ca2+信号传导中时空动力学的分子基础

Molecular basis of spatio-temporal dynamics in inositol 1,4,5-trisphosphate-mediated Ca2+ signalling.

作者信息

Iino M

机构信息

Department of Pharmacology, Graduate School of Medicine, University of Tokyo, Japan.

出版信息

Jpn J Pharmacol. 2000 Jan;82(1):15-20. doi: 10.1254/jjp.82.15.

Abstract

Inositol 1,4,5-trisphosphate (IP3)-mediated Ca2+ signalling regulates many important cell functions, and the spatio-temporal dynamics of the Ca2+ signalling is a crucial factor for its versatility. The molecular mechanisms that control Ca2+ signalling are now being investigated, and I here describe the subtypes of IP3 receptors that have distinct functional properties and contribute to the diversity of Ca2+ signalling patterns. I also discuss the spatio-temporal dynamics of intracellular IP3 concentration, describing recent methodological advances in monitoring intracellular IP3 concentration. These findings highlight the potential importance of the spatio-temporal information of any signalling molecule.

摘要

肌醇1,4,5-三磷酸(IP3)介导的Ca2+信号传导调节许多重要的细胞功能,而Ca2+信号传导的时空动态是其多功能性的关键因素。目前正在研究控制Ca2+信号传导的分子机制,我在此描述具有不同功能特性并导致Ca2+信号模式多样性的IP3受体亚型。我还讨论了细胞内IP3浓度的时空动态,介绍了监测细胞内IP3浓度的最新方法进展。这些发现突出了任何信号分子时空信息的潜在重要性。

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