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成骨细胞中液流诱导钙响应:数学建模。

Fluid flow induced calcium response in osteoblasts: mathematical modeling.

机构信息

Biomedical Engineering and Biomechanics Center, School of Aerospace, Xi'an Jiaotong University, 710049 Xi'an, PR China.

出版信息

J Biomech. 2011 Jul 28;44(11):2040-6. doi: 10.1016/j.jbiomech.2011.05.004. Epub 2011 Jun 12.

DOI:10.1016/j.jbiomech.2011.05.004
PMID:21665208
Abstract

Fluid flow in the bone lacuno-canalicular network can induce dynamic fluctuation of intracellular calcium concentration (Ca(2+)) in osteoblasts, which plays an important role in bone remodeling. There has been limited progress in the mathematical modeling of this process probably due to its complexity, which is controlled by various factors such as Ca(2+) channels and extracellular messengers. In this study we developed a mathematical model to describe Ca(2+) response induced by fluid shear stress (SS) by integrating the major factors involved and analyzed the effects of different experimental setups (e.g. Ca(2+) baseline, pretreatment with ATP). In this model we considered the ATP release process and the activities of multiple ion channels and purinergic receptors. The model was further verified quantitatively by comparing the simulation results with experimental data reported in literature. The results showed that: (i) extracellular ATP concentration has more significant effect on Ca(2+) baseline (73% increase in Ca(2+) with extracellular ATP concentration varying between 0 and 10 μM), as compared to that induced by SS (25% variation in Ca(2+) with SS varying from 0 to 3.5 Pa); (ii) Pretreatment with ATP-medium results in different Ca(2+) response as compared to the control group (ATP-free medium) under SS; (iii) Relative Ca(2+) fluctuation over baseline is more reliable to show the Ca(2+) response process than the absolute Ca(2+) response peak. The developed model may improve the experimental design and facilitate our understanding of the mechanotransduction process in osteoblasts.

摘要

骨陷窝-小管网络中的液体流动可以诱导成骨细胞内钙离子浓度 (Ca(2+)) 的动态波动,这在骨重塑中起着重要作用。由于该过程受到各种因素的控制,如 Ca(2+) 通道和细胞外信使,其数学建模进展有限。在这项研究中,我们通过整合涉及的主要因素,开发了一个数学模型来描述由流体切应力 (SS) 引起的 Ca(2+) 响应,并分析了不同实验设置的影响(例如 Ca(2+) 基线、用 ATP 预处理)。在这个模型中,我们考虑了 ATP 的释放过程以及多种离子通道和嘌呤能受体的活性。该模型通过将模拟结果与文献中报道的实验数据进行定量比较进一步得到验证。结果表明:(i) 与 SS 诱导的 Ca(2+) 变化(SS 从 0 增加到 3.5 Pa 时,Ca(2+) 变化 25%)相比,细胞外 ATP 浓度对 Ca(2+) 基线(细胞外 ATP 浓度在 0 到 10 μM 之间时,Ca(2+) 增加 73%)有更显著的影响;(ii) 与对照组(无 ATP 培养基)相比,SS 下用 ATP-培养基预处理会导致不同的 Ca(2+) 反应;(iii) 与绝对 Ca(2+) 响应峰值相比,相对 Ca(2+) 波动超过基线更能可靠地显示 Ca(2+) 响应过程。所开发的模型可以改进实验设计,有助于我们理解成骨细胞中的机械转导过程。

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