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On the Evolution of the Cardiac Pacemaker

机译:心脏起搏器的演变

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The rhythmic contraction of the heart is initiated and controlled by an intrinsic pacemaker system. Cardiac contractions commence at very early embryonic stages and coordination remains crucial for survival. The underlying molecular mechanisms of pacemaker cell development and function are still not fully understood. Heart form and function show high evolutionary conservation. Even in simple contractile cardiac tubes in primitive invertebrates, cardiac function is controlled by intrinsic, autonomous pacemaker cells. Understanding the evolutionary origin and development of cardiac pacemaker cells will help us outline the important pathways and factors involved. Key patterning factors, such as the homeodomain transcription factors Nkx2.5 and Shox2, and the LIM-homeodomain transcription factor Islet-1, components of the T-box (Tbx), and bone morphogenic protein (Bmp) families are well conserved. Here we compare the dominant pacemaking systems in various organisms with respect to the underlying molecular regulation. Comparative analysis of the pathways involved in patterning the pacemaker domain in an evolutionary context might help us outline a common fundamental pacemaker cell gene programme. Special focus is given to pacemaker development in zebrafish, an extensively used model for vertebrate development. Finally, we conclude with a summary of highly conserved key factors in pacemaker cell development and function.
机译:心脏的节律性收缩由内在的起搏器系统启动和控制。心脏收缩始于非常早期的胚胎阶段,协调对于存活至关重要。起搏器细胞发育和功能的潜在分子机制仍不完全清楚。心脏的形态和功能显示出高度的进化保守性。即使在原始无脊椎动物中的简单可收缩心脏管中,心脏功能也由内在的自主起搏器细胞控制。了解心脏起搏器细胞的进化起源和发展将帮助我们概述涉及的重要途径和因素。关键构型因子,例如同源域转录因子Nkx2.5和Shox2,以及LIM-同源域转录因子Islet-1,T-box(Tbx)的成分和骨形态发生蛋白(Bmp)家族,都得到了很好的保守。在这里,我们就潜在的分子调控比较了各种生物体中主要的起搏系统。在进化背景下对构图起搏器结构域的途径进行比较分析,可能有助于我们概述一个共同的基本起搏器细胞基因程序。特别关注斑马鱼的起搏器开发,这是脊椎动物发育的一种广泛使用的模型。最后,我们总结了起搏器细胞发育和功能中高度保守的关键因素。

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