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Gi2 and protein kinase C are required for thyrotropin-releasing hormone-induced stimulation of voltage-dependent Ca2+ channels in rat pituitary GH3 cells.Gi2和蛋白激酶C是促甲状腺激素释放激素诱导大鼠垂体GH3细胞中电压依赖性Ca2+通道刺激所必需的。
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促甲状腺激素释放激素对大鼠垂体GH3细胞中单个L型钙通道的刺激作用。

Stimulation of single L-type calcium channels in rat pituitary GH3 cells by thyrotropin-releasing hormone.

作者信息

Mantegazza M, Fasolato C, Hescheler J, Pietrobon D

机构信息

Department of Experimental Biomedical Sciences, University of Padova, Italy.

出版信息

EMBO J. 1995 Mar 15;14(6):1075-83. doi: 10.1002/j.1460-2075.1995.tb07090.x.

DOI:10.1002/j.1460-2075.1995.tb07090.x
PMID:7720698
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC398184/
Abstract

Hormonal stimulation of voltage-dependent Ca2+ channels in pituitary cells is thought to contribute to the sustained phase of Ca2+ entry and secretion induced by secretion stimulating hormones and has been suggested as a mechanism for refilling the Ca2+ stores. Using the cell-attached patch-clamp technique, we studied the stimulation of single Ca2+ channels by thyrotropin-releasing hormone (TRH) in rat GH3 cells. We show that TRH applied from the bath switched the activity of single L-type Ca2+ channels from a gating mode with very low open probability (po) to a gating mode with slightly smaller conductance but 10 times higher po. Interconversions between these two gating modes were also observed under basal conditions, where the equilibrium was shifted towards the low po mode. TRH applied from the pipette had no effect, indicating the involvement of a cytosolic compound in the stimulatory pathway. We show that TRH does not potentiate all the L-type Ca2+ channels in a given membrane patch and report evidence for co-expression of two functionally different L-type Ca2+ channels. Our results uncover the biophysical mechanism of hormonal stimulation of voltage-dependent Ca2+ channels in GH3 cells and are consistent with differential modulation of different subtypes of dihydropyridine-sensitive Ca2+ channels.

摘要

垂体细胞中电压依赖性Ca2+通道的激素刺激被认为有助于分泌刺激激素诱导的Ca2+内流和分泌的持续阶段,并被认为是补充Ca2+储存的一种机制。我们使用细胞贴附式膜片钳技术,研究了促甲状腺激素释放激素(TRH)对大鼠GH3细胞中单个Ca2+通道的刺激作用。我们发现,从浴槽中施加的TRH将单个L型Ca2+通道的活动从开放概率(po)非常低的门控模式转换为电导略小但po高10倍的门控模式。在基础条件下也观察到这两种门控模式之间的相互转换,此时平衡向低po模式偏移。从微管中施加的TRH没有效果,表明刺激途径中涉及一种胞质化合物。我们发现TRH不会增强给定膜片中的所有L型Ca2+通道,并报告了两种功能不同的L型Ca2+通道共表达的证据。我们的结果揭示了GH3细胞中电压依赖性Ca2+通道激素刺激的生物物理机制,并且与二氢吡啶敏感Ca2+通道不同亚型的差异调节一致。