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细胞质纳米空间在平滑肌细胞 Ca2+信号转导中的作用。

The role of cytoplasmic nanospaces in smooth muscle cell Ca2+ signalling.

机构信息

Department of Anesthesiology, Pharmacology and Therapeutics, The University of British Columbia, 2176, Health Sciences Mall, Vancouver, BC, Canada.

出版信息

Protoplasma. 2012 Feb;249 Suppl 1:S39-48. doi: 10.1007/s00709-011-0348-4. Epub 2011 Nov 9.

Abstract

We address the importance of cytoplasmic nanospaces in Ca(2+) transport and signalling in smooth muscle cells and how quantitative modelling can shed significant light on the understanding of signalling mechanisms. Increasingly more convincing evidence supports the view that these nanospaces--nanometre-scale spaces between organellar membranes, hosting cell signalling machinery--are key to Ca(2+) signalling as much as Ca(2+) transporters and Ca(2+) storing organelles. Our research suggests that the origin of certain diseases is to be sought in the disruption of the proper functioning of cytoplasmic nanospaces. We begin with a historical perspective on the study of smooth muscle cell plasma membrane-sarcoplasmic reticulum nanospaces, including experimental evidence of their role in the generation of asynchronous Ca(2+) waves. We then summarize how stochastic modelling approaches have aided and guided our understanding of two basic functional steps leading to healthy smooth muscle cell contraction. We furthermore outline how more sophisticated and realistic quantitative stochastic modelling is now being employed not only to deepen our understanding but also to aid in the hypothesis generation for further experimental investigation.

摘要

我们探讨了细胞质纳米空间在平滑肌细胞中钙(Ca2+)转运和信号转导中的重要性,以及定量建模如何为理解信号转导机制提供重要线索。越来越多令人信服的证据支持这样一种观点,即这些纳米空间——细胞器膜之间的纳米级空间,容纳着细胞信号转导机制——对于 Ca2+信号转导与 Ca2+转运体和 Ca2+储存细胞器同样重要。我们的研究表明,某些疾病的起源可以追溯到细胞质纳米空间正常功能的破坏。我们首先从平滑肌细胞膜-肌浆网纳米空间研究的历史角度出发,包括其在产生异步 Ca2+波中的作用的实验证据。然后,我们总结了随机建模方法如何帮助和指导我们理解导致健康平滑肌细胞收缩的两个基本功能步骤。此外,我们还概述了如何采用更复杂和现实的定量随机建模方法,不仅加深我们的理解,还为进一步的实验研究生成假说提供帮助。

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