Center for Biomedical Engineering and Technology, University of Maryland, Baltimore, Maryland, USA.
Biophys J. 2011 Sep 21;101(6):1287-96. doi: 10.1016/j.bpj.2011.07.021. Epub 2011 Sep 20.
We present what we believe to be a new mathematical model of Ca(2+) leak from the sarcoplasmic reticulum (SR) in the heart. To our knowledge, it is the first to incorporate a realistic number of Ca(2+)-release units, each containing a cluster of stochastically gating Ca(2+) channels (RyRs), whose biophysical properties (e.g., Ca(2+) sensitivity and allosteric interactions) are informed by the latest molecular investigations. This realistic model allows for the detailed characterization of RyR Ca(2+)-release properties, and shows how this balances reuptake by the SR Ca(2+) pump. Simulations reveal that SR Ca(2+) leak consists of brief but frequent single RyR openings (3000 cell(-1) s(-1)) that are likely to be experimentally undetectable, and are, therefore, "invisible". We also observe that these single RyR openings can recruit additional RyRs to open, due to elevated local (Ca(2+)), and occasionally lead to the generation of Ca(2+) sparks (130 cell(-1) s(-1)). Furthermore, this physiological formulation of "invisible" leak allows for the removal of the ad hoc, non-RyR mediated Ca(2+) leak terms present in prior models. Finally, our model shows how Ca(2+) sparks can be robustly triggered and terminated under both normal and pathological conditions. Together, these discoveries profoundly influence how we interpret and understand diverse experimental and clinical results from both normal and diseased hearts.
我们提出了一个新的 Ca(2+) 从心肌肌浆网(SR)中漏出的数学模型。据我们所知,这是第一个包含真实数量的 Ca(2+) 释放单元的模型,每个释放单元包含一组随机门控的 Ca(2+) 通道(RyRs),其生物物理特性(例如 Ca(2+) 敏感性和变构相互作用)是由最新的分子研究提供的。这个现实的模型允许详细表征 RyR Ca(2+) 释放特性,并展示了如何平衡 SR Ca(2+) 泵的再摄取。模拟结果表明,SR Ca(2+) 泄漏由短暂但频繁的单个 RyR 开放(3000 个细胞(-1) s(-1))组成,这些开放可能在实验中无法检测到,因此是“不可见的”。我们还观察到,由于局部 Ca(2+) 的升高,这些单个 RyR 开放可以招募额外的 RyR 开放,并且偶尔会导致 Ca(2+) 火花的产生(130 个细胞(-1) s(-1))。此外,这种“不可见”泄漏的生理表述允许从之前的模型中去除特定的、非 RyR 介导的 Ca(2+) 泄漏项。最后,我们的模型展示了在正常和病理条件下,Ca(2+) 火花如何能够被稳健地触发和终止。总之,这些发现深刻地影响了我们如何解释和理解来自正常和患病心脏的各种实验和临床结果。