首页> 外文期刊>Journal of General Physiology >Intracellular Ca~(2+) Oscillations, a Potential Pacemaking Mechanism in Early Embryonic Heart Cells
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Intracellular Ca~(2+) Oscillations, a Potential Pacemaking Mechanism in Early Embryonic Heart Cells

机译:细胞内Ca〜(2+)振荡,早期胚胎心脏细胞的潜在起搏机制。

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Early (E9.5-E11.5) embryonic heart cells beat spontaneously, even though the adult pacemaking mechanisms are not yet fully established. Here we show that in isolated murine early embryonic cardiomyocytes periodic oscillations of cytosolic Ca~(2+) occur and that these induce contractions. The Ca~(2+) oscillations originate from the sarcoplas-mic reticulum and are dependent on the on the IP_3 and the ryanodine receptor. The Ca~(2+) oscillations activate the Na~+-Ca~(2+) exchanger, giving rise to subthreshold depolarizations of the membrane potential and/or action potentials. Although early embryonic heart cells are voltage-independent Ca~(2+) oscillators, the generation of action potentials provides synchronization of the electrical and mechanical signals. Thus, Ca~(2+) oscillations pace early embryonic heart cells and the ensuing activation of the Na~+-Ca~(2+) exchanger evokes small membrane depolarizations or action potentials.
机译:即使成人起搏机制尚未完全建立,早期(E9.5-E11.5)胚胎心脏细胞也会自发搏动。在这里,我们表明在孤立的小鼠早期胚胎心肌细胞中发生胞质Ca〜(2+)的周期性振荡,并且这些振荡诱导收缩。 Ca〜(2+)振荡起源于斜纹肌网,并取决于IP_3和ryanodine受体。 Ca〜(2+)振荡会激活Na〜+ -Ca〜(2+)交换子,从而引起膜电位和/或动作电位的亚阈值去极化。尽管早期的胚胎心脏细胞是不依赖电压的Ca〜(2+)振荡器,但是动作电位的产生提供了电信号和机械信号的同步。因此,Ca〜(2+)振荡加快了早期胚胎心脏细胞的步伐,随后的Na〜+ -Ca〜(2+)交换子的激活引起了小的膜去极化或动作电位。

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