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钙诱导钙释放局部控制的多尺度模型。

Multi-scale models of local control of calcium induced calcium release.

作者信息

Hinch R, Greenstein J L, Winslow R L

机构信息

Center for Cardiovascular Bioinformatics and Modeling, The John's Hopkins University School of Medicine and Whiting School of Engineering, Baltimore, MD, USA.

出版信息

Prog Biophys Mol Biol. 2006 Jan-Apr;90(1-3):136-50. doi: 10.1016/j.pbiomolbio.2005.05.014.

Abstract

Calcium-induced-calcium-release in cardiac myocytes is the release of Ca(2+) from the sarcoplasmic reticulum (SR) triggered by Ca(2+) entering the cell through L-type Ca(2+) channels. The Ca(2+) is released through ryanodine receptors which 'sense' local [Ca(2+)] in the small region (the diadic space) positioned between the t-tubules and the SR. The length-scale of a single diad is of the order of 10nm and the diffusion time-scale is of order of 1 micros with each cell containing approximately 10,000 diadic spaces which act independently. However, typically one is interested in Ca(2+) currents at the whole cell level and higher. This is a multi-scale problem and cannot be solved by direct computation. In this paper we develop a general framework for deriving approximate solutions of these models.

摘要

心肌细胞中的钙诱导钙释放是指由通过L型钙通道进入细胞的Ca(2+)触发肌浆网(SR)释放Ca(2+)。Ca(2+)通过雷诺丁受体释放,这些受体“感知”位于横管和肌浆网之间的小区域(二联体空间)中的局部[Ca(2+)]。单个二联体的长度尺度约为10nm,扩散时间尺度约为1微秒,每个细胞包含约10,000个独立起作用的二联体空间。然而,通常人们感兴趣的是整个细胞水平及更高水平的Ca(2+)电流。这是一个多尺度问题,无法通过直接计算解决。在本文中,我们开发了一个用于推导这些模型近似解的通用框架。

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