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Kv1.3 钾通道的生理机能可通过遗传和药理学调节进行评估。

Kv1.3 K Channel Physiology Assessed by Genetic and Pharmacological Modulation.

机构信息

Department of Biology, University of Padova, Padova, Italy.

出版信息

Physiology (Bethesda). 2023 Jan 1;38(1):0. doi: 10.1152/physiol.00010.2022. Epub 2022 Aug 23.

Abstract

Potassium channels are widespread over all kingdoms and play an important role in the maintenance of cellular ionic homeostasis. Kv1.3 is a voltage-gated potassium channel of the Shaker family with a wide tissue expression and a well-defined pharmacology. In recent decades, experiments mainly based on pharmacological modulation of Kv1.3 have highlighted its crucial contribution to different fundamental processes such as regulation of proliferation, apoptosis, and metabolism. These findings link channel function to various pathologies ranging from autoimmune diseases to obesity and cancer. In the present review, we briefly summarize studies employing Kv1.3 knockout animal models to confirm such roles and discuss the findings in comparison to the results obtained by pharmacological modulation of Kv1.3 in various pathophysiological settings. We also underline how these studies contributed to our understanding of channel function in vivo and propose possible future directions.

摘要

钾通道广泛存在于所有生物界,在维持细胞离子稳态方面发挥着重要作用。Kv1.3 是 Shaker 家族的一种电压门控钾通道,具有广泛的组织表达和明确的药理学特性。在过去的几十年中,主要基于药理学调节 Kv1.3 的实验强调了其对不同基本过程(如增殖、凋亡和代谢的调节)的关键贡献。这些发现将通道功能与从自身免疫性疾病到肥胖和癌症等各种病理联系起来。在本综述中,我们简要总结了使用 Kv1.3 基因敲除动物模型的研究,以证实这些作用,并讨论了与在各种病理生理环境中通过药理学调节 Kv1.3 获得的结果的比较。我们还强调了这些研究如何有助于我们理解体内通道功能,并提出了可能的未来方向。

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