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T型α1H钙离子通道参与人类成肌细胞终末分化(融合)过程中的钙离子信号传导。

T-type alpha 1H Ca2+ channels are involved in Ca2+ signaling during terminal differentiation (fusion) of human myoblasts.

作者信息

Bijlenga P, Liu J H, Espinos E, Haenggeli C A, Fischer-Lougheed J, Bader C R, Bernheim L

机构信息

Département de Physiologie, Centre Médical Universitaire, and Division de Recherche Clinique Neuro-Musculaire, Hôpital Cantonal Universitaire, CH-1211 Geneva 4, Switzerland.

出版信息

Proc Natl Acad Sci U S A. 2000 Jun 20;97(13):7627-32. doi: 10.1073/pnas.97.13.7627.

Abstract

Mechanisms underlying Ca(2+) signaling during human myoblast terminal differentiation were studied using cell cultures. We found that T-type Ca(2+) channels (T-channels) are expressed in myoblasts just before fusion. Their inhibition by amiloride or Ni(2+) suppresses fusion and prevents an intracellular Ca(2+) concentration increase normally observed at the onset of fusion. The use of antisense oligonucleotides indicates that the functional T-channels are formed by alpha1H subunits. At hyperpolarized potentials, these channels allow a window current sufficient to increase Ca(2+). As hyperpolarization is a prerequisite to myoblast fusion, we conclude that the Ca(2+) signal required for fusion is produced when the resting potential enters the T-channel window. A similar mechanism could operate in other cell types of which differentiation implicates membrane hyperpolarization.

摘要

利用细胞培养技术研究了人类成肌细胞终末分化过程中Ca(2+)信号传导的潜在机制。我们发现,T型Ca(2+)通道(T通道)在成肌细胞融合前就已表达。氨氯地平或Ni(2+)对它们的抑制作用会抑制融合,并阻止通常在融合开始时观察到的细胞内Ca(2+)浓度升高。反义寡核苷酸的使用表明功能性T通道由α1H亚基形成。在超极化电位下,这些通道允许产生足以增加[Ca(2+)]i的窗电流。由于超极化是成肌细胞融合的先决条件,我们得出结论,当静息电位进入T通道窗口时,会产生融合所需的Ca(2+)信号。类似的机制可能在其他分化涉及膜超极化的细胞类型中起作用。

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