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Role of voltage‐gated calcium channels in the regulation of aldosterone production from zona glomerulosa cells of the adrenal cortex

机译:电压门控钙通道在肾上腺皮质肾小球细胞醛固酮产生的调节中的作用

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摘要

Zona glomerulosa cells (ZG) of the adrenal gland constantly integrate fluctuating ionic, hormonal and paracrine signals to control the synthesis and secretion of aldosterone. These signals modulate Ca2+ levels, which provide the critical second messenger to drive steroid hormone production. Angiotensin II is a hormone known to modulate the activity of voltage‐dependent L‐ and T‐type Ca2+ channels that are expressed on the plasma membrane of ZG cells in many species. Because the ZG cell maintains a resting membrane voltage of approximately −85 mV and has been considered electrically silent, low voltage‐activated T‐type Ca2+ channels are assumed to provide the primary Ca2+ signal that drives aldosterone production. However, this view has recently been challenged by human genetic studies identifying somatic gain‐of‐function mutations in L‐type CaV1.3 channels in aldosterone‐producing adenomas of patients with primary hyperaldosteronism. We provide a review of these assumptions and challenges, and update our understanding of the state of the ZG cell in a layer in which native cellular associations are preserved. This updated view of Ca2+ signalling in ZG cells provides a unifying mechanism that explains how transiently activating CaV3.2 channels can generate a significant and recurring Ca2+ signal, and how CaV1.3 channels may contribute to the Ca2+ signal that drives aldosterone production.
机译:肾上腺的Zona肾小球细胞(ZG)不断整合波动的离子,激素和旁分泌信号,以控制醛固酮的合成和分泌。这些信号调节Ca 2 + 的水平,为驱动类固醇激素的产生提供关键的第二信使。血管紧张素II是一种已知的激素,可调节许多物种的ZG细胞质膜上表达的电压依赖性L和T型Ca 2 + 通道的活性。由于ZG电池维持约-85 mV的静止膜电压并被认为是电静默的,因此假定低压激活的T型Ca 2 + 通道可提供主要的Ca 2 + 信号驱​​动醛固酮的产生。但是,这种观点最近受到人类遗传研究的挑战,该研究确定了原发性醛固酮过多症患者的醛固酮生成腺瘤中L型CaV1.3通道的体细胞功能获得性突变。我们提供了对这些假设和挑战的回顾,并更新了我们对保留天然细胞关联的一层中ZG细胞状态的理解。 ZG细胞中Ca 2 + 信号的更新视图提供了一种统一的机制,该机制解释了瞬时激活CaV3.2通道如何产生显着且重复出现的Ca 2 + 信号,以及CaV1.3通道如何影响驱动醛固酮生成的Ca 2 + 信号。

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