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The effect of bioenergetic impairment of cytosolic processes in spatio-temporal Ca²⁺ dynamics in a three-dimensional cardiomyocyte model

机译:三维心肌细胞模型中细胞溶质过程的生物能量损伤对时空Ca2 +动力学的影响

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摘要

The heart consumes large amounts of energy with each beat. Mitochondria are the source of over 95% of this energy in the form of ATP and rely on increased Ca²⁺ uptake to stimulate production in times of increased work. Ca²⁺ uptake into the mitochondria primarily occurs within microdomains. Structural remodeling associated with heart failure may disrupt these microdomains leading to impaired mitochondrial Ca²⁺ uptake and energetic impairment. To investigate the effect of structural changes on single cell behavior, a model describing mitochondrial dynamics and energetics production is modified and incorporated into a recently developed three-dimensional model of spatio-temporal calcium handling, which preserves microdomain structure and incorporates stochastic processes in Ca²⁺ handling protein kinetics. Modifications to the mitochondria model included a reformulation of mitochondrial Ca²⁺ uniporter uptake, making it suitable for concentrations in microdomains. With this model we demonstrate the importance of an ordered structure within the cell for normal function. Changes in the arrangement of mitochondria can have a pronounced effect on intracellular Ca²⁺ dynamics through their energetic regulation of SERCA, leading to spatially heterogeneous sarcoplasmic reticulum uptake and loading.
机译:每次跳动,心脏都会消耗大量能量。线粒体以ATP的形式来消耗此能量的95%以上,并且在增加工作量时依靠增加的Ca 2+吸收来刺激生产。线粒体对Ca 2+的吸收主要发生在微区中。与心力衰竭相关的结构重塑可能会破坏这些微区,从而导致线粒体Ca 2+吸收受损和精力充沛。为了研究结构变化对单细胞行为的影响,对描述线粒体动力学和高能产生的模型进行了修改,并将其纳入最近开发的时空钙处理三维模型中,该模型保留了微区结构并在Ca²2中纳入了随机过程。处理蛋白质动力学。线粒体模型的修改包括重新设计线粒体Ca²2单向摄取,使其适用于微区中的浓度。通过这个模型,我们证明了细胞内有序结构对于正常功能的重要性。线粒体排列的变化可通过其对SERCA的有力调节,对细胞内Ca 2+动力学产生显着影响,导致空间异质性肌质网的摄取和负载。

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  • 作者

    Jones GM; Zhang H; Colman MA;

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  • 年度 2017
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  • 原文格式 PDF
  • 正文语种 en
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