首页> 外文期刊>The Journal of general physiology >Intracellular Ca2+ Oscillations, a Potential Pacemaking Mechanism in Early Embryonic Heart Cells
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Intracellular Ca2+ Oscillations, a Potential Pacemaking Mechanism in Early Embryonic Heart Cells

机译:细胞内Ca 2+振荡,早期胚胎心脏细胞中潜在的起搏机制。

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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 Ca2+ occur and that these induce contractions. The Ca2+ oscillations originate from the sarcoplasmic reticulum and are dependent on the IP3 and the ryanodine receptor. The Ca2+ oscillations activate the Na+-Ca2+ exchanger, giving rise to subthreshold depolarizations of the membrane potential and/or action potentials. Although early embryonic heart cells are voltage-independent Ca2+ oscillators, the generation of action potentials provides synchronization of the electrical and mechanical signals. Thus, Ca2+ oscillations pace early embryonic heart cells and the ensuing activation of the Na+-Ca2+ exchanger evokes small membrane depolarizations or action potentials.
机译:早期(E9.5–E11.5)胚胎心脏细胞会自发搏动,即使成人起搏机制尚未完全建立。在这里,我们表明在孤立的鼠类早期胚胎心肌细胞中会发生胞质Ca2 +的周期性振荡,并且这些振荡会引起收缩。 Ca2 +振荡起源于肌浆网,并依赖于IP3和ryanodine受体。 Ca2 +振荡会激活Na + -Ca2 +交换剂,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Ca2 +振荡器,但动作电位的产生提供了电信号和机械信号的同步。因此,Ca2 +振荡会加快早期胚胎心脏细胞的步伐,随后的Na + -Ca2 +交换子的激活引起小的膜去极化或动作电位。

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