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Ca2+ spark dynamics in cardiac myocyte

机译:心肌细胞中Ca2 +火花动力学

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Ca2+, one of the most classical messengers in living cells, regulates many important life processes, from hormone secretion to muscle contraction, nerve signal transduction to learning and memory, gene expression to protein phosphorylation. But how can Ca2+ take on such a wide range of physiological functions? The relations among these functions, sorts of Ca2+ channels, space distribution, kinetic control, and Ca2+ buffering and diffusion in cell microenvironment, are essential problems for research on Ca2+ signal transduction and important foundation for elucidating cell function, growth, signal process and pathology. Cheng et al. first demonstrated that Ca2+ release from the sarcoplasmic reticulum (SR) occurs as discrete quanta[1]. They named these quanta Ca2+ sparks because of the brief localized light emission they induced in Ca2+sensitive fluorescent dyes. Since their discovery, Ca2+ sparks have been found in cardiac, skeletal, and smooth muscle cells and provide molecular interpretations for intercellular Ca2+ signal transduction[2-4]. However, in the opinion of biomechanics, Ca2+ spark is a dynamic process of random point source diffusion and chemical reactions of substances in the cell. The classical Fickian diffusion e-quation and reaction-kinetic model have been widely used to describe the process. However, recent work suggests that even the minimum spatial scale of Ca2+ spark is still much larger than that simulated by the Fickian diffusion model [5]. Based on the diffusion phenomenon of Ca2+ spark in cardiac myocytes, an essential question on unit calcium signal has been put forward: whether the diffusion of calcium spark obeys Fickian diffusion, if not, why? Furthermore, which rule and theory can best describe kinetics of this anomalous diffusion. These are very important to elucidate how Ca2+ molecular channel produces gradient of calcium signal, how different gradients activate different target sites and downstream signal pathway, and consequently control different life process in the cell.
机译:Ca2 +是活细胞中最经典的信使之一,它调节着许多重要的生命过程,从激素分泌到肌肉收缩,从神经信号转导到学习和记忆,从基因表达到蛋白质磷酸化。但是Ca2 +如何承担如此广泛的生理功能?这些功能之间的关系,Ca2 +通道的种类,空间分布,动力学控制以及细胞微环境中Ca2 +的缓冲和扩散,是研究Ca2 +信号转导的基本问题,也是阐明细胞功能,生长,信号过程和病理的重要基础。程等。首次证明,从肌质网(SR)释放的Ca2 +以离散量子的形式出现[1]。他们称这些量子为Ca2 +火花是因为它们在对Ca2 +敏感的荧光染料中引起的短暂的局部发光。自发现以来,就在心脏,骨骼和平滑肌细胞中发现了Ca2 +火花,并为细胞间Ca2 +信号转导提供了分子解释[2-4]。然而,从生物力学的观点来看,Ca 2+火花是随机点源扩散和细胞中物质化学反应的动态过程。经典的Fickian扩散方程和反应动力学模型已被广泛用于描述该过程。但是,最近的工作表明,即使是Ca2 +火花的最小空间尺度仍然比Fickian扩散模型所模拟的空间尺度大得多[5]。基于心肌细胞中Ca2 +火花的扩散现象,提出了有关单位钙信号的基本问题:钙火花的扩散是否服从菲克扩散,如果不是,为什么?此外,哪种规则和理论可以最好地描述这种异常扩散的动力学。这些对于阐明Ca2 +分子通道如何产生钙信号梯度,不同的梯度如何激活不同的靶位点和下游信号通路,从而控制细胞中不同的生命过程非常重要。

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