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胰腺腺泡细胞中钙振荡的建模机制。

Modelling mechanism of calcium oscillations in pancreatic acinar cells.

作者信息

Manhas Neeraj, Pardasani K R

机构信息

Department of Applied Mathematics, Maulana Azad National Institute of Technology, 462051, Bhopal, India,

出版信息

J Bioenerg Biomembr. 2014 Oct;46(5):403-20. doi: 10.1007/s10863-014-9561-0. Epub 2014 Jul 11.

Abstract

We present a simple model for calcium oscillations in the pancreatic acinar cells. This model is based on the calcium release from two receptors, inositol trisphosphate receptors (IPR) and ryanodine receptors (RyR) through the process of calcium induced calcium release (CICR). In pancreatic acinar cells, when the Ca²⁺ concentration increases, the mitochondria uptake it very fast to restrict Ca(2+) response in the cell. Afterwards, a much slower release of Ca²⁺ from the mitochondria serves as a calcium supply in the cytosol which causes calcium oscillations. In this paper we discuss a possible mechanism for calcium oscillations based on the interplay among the three calcium stores in the cell: the endoplasmic reticulum (ER), mitochondria and cytosol. Our model predicts that calcium shuttling between ER and mitochondria is a pacemaker role in the generation of Ca²⁺ oscillations. We also consider the calcium dependent production and degradation of (1,4,5) inositol-trisphosphate (IP3), which is a key source of intracellular calcium oscillations in pancreatic acinar cells. In this study we are able to predict the different patterns of calcium oscillations in the cell from sinusoidal to raised-baseline, high frequency and low-frequency baseline spiking.

摘要

我们提出了一个用于胰腺腺泡细胞钙振荡的简单模型。该模型基于通过钙诱导钙释放(CICR)过程从两种受体,即肌醇三磷酸受体(IPR)和兰尼碱受体(RyR)释放钙。在胰腺腺泡细胞中,当Ca²⁺浓度增加时,线粒体非常快速地摄取它以限制细胞内的Ca(2+)反应。之后,线粒体中Ca²⁺的释放要慢得多,它作为细胞质中的钙供应源,从而引起钙振荡。在本文中,我们讨论了基于细胞中三种钙库,即内质网(ER)、线粒体和细胞质之间相互作用的钙振荡可能机制。我们的模型预测,内质网和线粒体之间的钙穿梭在Ca²⁺振荡的产生中起起搏器作用。我们还考虑了(1,4,5)肌醇三磷酸(IP3)的钙依赖性产生和降解,IP3是胰腺腺泡细胞中细胞内钙振荡的关键来源。在这项研究中,我们能够预测细胞中从正弦波到升高基线、高频和低频基线尖峰的不同钙振荡模式。

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