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首页> 外文期刊>Physics Letters, A >Genetically engineered cardiac pacemaker: Stem cells transfected with HCN2 gene and myocytes - A model
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Genetically engineered cardiac pacemaker: Stem cells transfected with HCN2 gene and myocytes - A model

机译:基因工程心脏起搏器:HCN2基因和心肌细胞转染的干细胞-模型

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摘要

One of the successfully tested methods to design genetically engineered cardiac pacemaker cells consists in transfecting a human mesenchymal stem cell (hMSC) with a HCN2 gene and connecting it to a myocyte. We develop and study a mathematical model, describing a myocyte connected to a hMSC transfected with a HCN2 gene. The cardiac action potential is described both with the simple Beeler-Reuter model, as well as with the elaborate dynamic Luo-Rudy model. The HCN2 channel is described by fitting electrophysiological records, in the spirit of Hodgkin-Huxley. The model shows that oscillations can occur in a pair myocyte-stem cell, that was not observed in the experiments yet. The model predicted that: (1) HCN pacemaker channels can induce oscillations only if the number of expressed IK1 channels is low enough. At too high an expression level of IK1 channels, oscillations cannot be induced, no matter how many pacemaker channels are expressed. (2) At low expression levels of IK1 channels, a large domain of values in the parameter space (n, N) exists, where oscillations should be observed. We denote N the number of expressed pacemaker channels in the stem cell, and n the number of gap junction channels coupling the stem cell and the myocyte. (3) The expression levels of IK1 channels observed in ventricular myocytes, both in the Beeler-Reuter and in the dynamic Luo-Rudy models are too high to allow to observe oscillations. With expression levels below similar to 4/4 of the original value, oscillations can be observed. The main consequence of this work is that in order to obtain oscillations in an experiment with a myocyte-stem cell pair, increasing the values of n, N is unlikely to be helpful, unless the expression level Of IK1 has been reduced enough. The model also allows us to explore levels of gene expression not yet achieved in experiments, and could be useful to plan new experiments, aimed at improving the robustness of the oscillations. (C) 2007 Elsevier B.V. All rights reserved.
机译:设计基因工程的心脏起搏器细胞的一种成功测试的方法包括用HCN2基因转染人间充质干细胞(hMSC)并将其连接到心肌细胞。我们开发和研究一种数学模型,描述了与转染了HCN2基因的hMSC连接的心肌细胞。简单的Beeler-Reuter模型以及复杂的动态Luo-Rudy模型都描述了心脏动作电位。按照Hodgkin-Huxley的精神,通过拟合电生理记录来描述HCN2通道。该模型显示在一对成肌干细胞中可能发生振荡,这在实验中还没有观察到。该模型预测:(1)仅当所表达的IK1通道的数量足够少时,HCN起搏器通道才能引起振荡。在IK1通道的表达水平过高时,无论表达多少个起搏器通道,都不会引起振荡。 (2)在IK1通道的低表达水平下,在参数空间(n,N)中存在一个较大的值域,应观察到振荡。我们将N表示在干细胞中表达的起搏器通道的数量,N表示将干细胞和心肌细胞偶联的间隙连接通道的数量。 (3)在Beeler-Reuter模型和动态Luo-Rudy模型中,在心室肌细胞中观察到的IK1通道的表达水平过高,无法观察到振荡。如果表达水平低于原始值的4/4,则可以观察到振荡。这项工作的主要结果是,为了在肌细胞-干细胞对的实验中获得振荡,增加n,N的值不太可能有帮助,除非IK1的表达水平已充分降低。该模型还允许我们探索实验中尚未达到的基因表达水平,并且对于计划新实验以提高振荡的鲁棒性可能有用。 (C)2007 Elsevier B.V.保留所有权利。

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