小鼠胚胎心脏初始收缩期的模式及测定。

Anatomy and Embryology Pub Date : 2006-03-01 Epub Date: 2005-11-30 DOI:10.1007/s00429-005-0065-x
Kiyomasa Nishii, Yosaburo Shibata
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引用次数: 47

摘要

发育中的哺乳动物心脏在心肌从内脏中胚层分化后不久就开始自发收缩。然而,在小鼠中,心跳的精确时间和模式还没有统计学上的描述。我们分析了录像记录的心脏区域从体前阶段到第10.5天的收缩活动模式。第一个征象出现在3-somite期(E8.25),此时在心管两侧有少量心肌细胞组成小的收缩群。在休眠3-somite阶段的心脏中检测到基础[Ca2+]i水平的波动,表明在可见收缩之前开始电活动。3-体期的收缩微弱而不规则,但早在4-体期收缩基本协调。E9.25时20岁左右房室管单向血流建立,与心内膜缓冲的形成相关。我们认为,不仅心内膜缓冲,而且协调收缩对单向血流至关重要,因为在室温下短时间暴露引起的心动过缓会导致E10.5时的反流,而在其他情况下观察到高度有组织的血流。这些发现补充和扩展了早期对心脏功能发育的观察,为哺乳动物心脏发生的基础研究提供了参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mode and determination of the initial contraction stage in the mouse embryo heart.

The developing mammalian heart initiates spontaneous contractions shortly after the myocardium differentiates from the splanchnic mesoderm. The precise timing and mode of the onset of heartbeat, however, have not been statistically described in mice. We analyzed the patterns of contractive activity in video-recorded heart regions ranging from the pre-somite stage to day 10.5 (E10.5). The first sign was detected at the 3-somite stage (E8.25), when a few cardiac myocytes constituted small contracting groups on both sides of the heart tube. Fluctuations of the basal [Ca2+]i level were detected in dormant 3-somite-stage hearts, indicating the initiation of electrical activity before visible contractions. After weak and irregular contractions at the 3-somite stage, the contractions were almost coordinated as early as the 4-somite stage. Unidirectional blood flow through the atrioventricular canal was established around the 20-somite stage at E9.25, correlated with the development of the endocardial cushion. We propose that not only the endocardial cushion but also coordinated contractions are essential for unidirectional flow, because induced bradycardia due to short exposure at room temperature caused regurgitation at E10.5 when otherwise highly organized flow was observed. These findings complement and extend earlier observations on functional heart development, providing a reference for fundamental research on mammalian cardiogenesis.

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