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GSK3β 通过调节腺苷酸环化酶活性介导肾对血管加压素的反应。

GSK3beta mediates renal response to vasopressin by modulating adenylate cyclase activity.

机构信息

Division of Nephrology and Hypertension, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee 37232, USA.

出版信息

J Am Soc Nephrol. 2010 Mar;21(3):428-37. doi: 10.1681/ASN.2009060672. Epub 2010 Jan 7.

Abstract

Glycogen synthase kinase 3beta (GSK3beta), a serine/threonine protein kinase, is a key target of drug discovery in several diseases, including diabetes and Alzheimer disease. Because lithium, a potent inhibitor of GSK3beta, causes nephrogenic diabetes insipidus, GSK3beta may play a crucial role in regulating water homeostasis. We developed renal collecting duct-specific GSK3beta knockout mice to determine whether deletion of GSK3beta affects arginine vasopressin-dependent renal water reabsorption. Although only mildly polyuric under normal conditions, knockout mice exhibited an impaired urinary concentrating ability in response to water deprivation or treatment with a vasopressin analogue. The knockout mice had reduced levels of mRNA, protein, and membrane localization of the vasopressin-responsive water channel aquaporin 2 compared with wild-type mice. The knockout mice also expressed lower levels of pS256-AQP2, a phosphorylated form crucial for membrane trafficking. Levels of cAMP, a major regulator of aquaporin 2 expression and trafficking, were also lower in the knockout mice. Both GSK3beta gene deletion and pharmacologic inhibition of GSK3beta reduced adenylate cyclase activity. In summary, GSK3beta inactivation or deletion reduces aquaporin 2 expression by modulating adenylate cyclase activity and cAMP generation, thereby impairing responses to vasopressin in the renal collecting duct.

摘要

糖原合酶激酶 3β(GSK3β)是一种丝氨酸/苏氨酸蛋白激酶,是包括糖尿病和阿尔茨海默病在内的多种疾病药物发现的关键靶点。由于强效 GSK3β抑制剂锂可引起肾性尿崩症,因此 GSK3β可能在调节水稳态方面发挥关键作用。我们开发了肾脏集合管特异性 GSK3β敲除小鼠,以确定 GSK3β缺失是否会影响精氨酸加压素依赖性肾脏水重吸收。尽管在正常情况下仅轻度多尿,但敲除小鼠在禁水或用血管加压素类似物治疗时表现出受损的尿浓缩能力。与野生型小鼠相比,敲除小鼠的 mRNA、蛋白和血管加压素反应性水通道 aquaporin 2 的膜定位减少。敲除小鼠还表达较低水平的 pS256-AQP2,这是一种对于膜运输至关重要的磷酸化形式。cAMP 的水平,一种主要调节 aquaporin 2 表达和运输的物质,在敲除小鼠中也较低。GSK3β基因缺失和 GSK3β 的药理学抑制均降低了腺苷酸环化酶活性。总之,GSK3β失活或缺失通过调节腺苷酸环化酶活性和 cAMP 的产生来减少 aquaporin 2 的表达,从而损害肾脏集合管对血管加压素的反应。

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本文引用的文献

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Adenylyl and guanylyl cyclase assays.腺苷酸环化酶和鸟苷酸环化酶测定。
Curr Protoc Pharmacol. 2005 Oct;Chapter 2:Unit2.2. doi: 10.1002/0471141755.ph0202s30.
2
Mice lacking mPGES-1 are resistant to lithium-induced polyuria.缺乏微粒体前列腺素E合酶-1的小鼠对锂诱导的多尿具有抗性。
Am J Physiol Renal Physiol. 2009 Dec;297(6):F1689-96. doi: 10.1152/ajprenal.00117.2009. Epub 2009 Aug 19.
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Aquaporin-2 protein dynamics within the cell.细胞内水通道蛋白2的蛋白质动力学
Curr Opin Nephrol Hypertens. 2007 Jul;16(4):348-52. doi: 10.1097/MNH.0b013e32818b27bf.

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