IP3R 和 nSOCE--两端相连。

Contact (Thousand Oaks (Ventura County, Calif.)) Pub Date : 2024-02-12 eCollection Date: 2024-01-01 DOI:10.1177/25152564241231092
Gaiti Hasan
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引用次数: 0

摘要

所有生物体都需要对细胞外环境的变化做出适当的反应。细胞内 Ca2+ 信号传导就是这样一种机制,细胞膜接收到的细胞外信号与内质网储存的 Ca2+ 相互传递,从而刺激细胞生理发生由 Ca2+ 介导的适当变化。内质网(ER)-Ca2+ 释放响应细胞外信号的幅度和动态决定了细胞反应的性质。目前还缺乏对不同类型细胞中 ER-Ca2+ 通道如何调节细胞 Ca2+ 信号转导的了解。最近的一篇论文以神经元为背景探讨了这一问题(Chakraborty 等人,2023 年),本文将讨论这些新发现的意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
IP3Rs and nSOCE-Tied Together at Two Ends.

All living organisms need to respond appropriately to changes in the extracellular milieu. Cellular mechanisms that enable such responses evolved in parallel with organismal complexity and intracellular Ca2+ signaling is one such mechanism where extracellular signals received at the cell membrane communicate with endoplasmic reticular stores of Ca2+, to stimulate appropriate Ca2+-mediated changes in cellular physiology. The amplitude and dynamics of endoplasmic reticulum (ER)-Ca2+ release in response to extracellular signals determines the nature of the cellular response. An understanding of how ER-Ca2+ channels might regulate cellular Ca2+ signaling in different cell types is lacking. In a recent paper, this question has been addressed in the context of neurons ( Chakraborty et al., 2023) and the implications of these new findings are discussed here.

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