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MST3(哺乳动物Ste20样蛋白激酶3),一种参与自发性高血压大鼠离子稳态和肾脏血压调节的新基因。

MST3 (mammalian Ste20-like protein kinase 3), a novel gene involved in ion homeostasis and renal regulation of blood pressure in spontaneous hypertensive rats.

作者信息

Lu Te-Jung, Chan Chee-Hong, Ling Pin, Chao Yung-Mei, Bao Bo-Ying, Chiang Chun-Yen, Lee Te-Hsiu, Weng Yui-Ping, Kan Wei-Chih, Lu Te-Ling

机构信息

Department of Medical Laboratory Science and Biotechnology, Chung-Hwa University of Medical Technology, Tainan, Taiwan.

Department of Nephrology, Chang Bing Show-Chwan Memorial Hospital, Lukang, Changhua, Taiwan.

出版信息

Int Urol Nephrol. 2018 Dec;50(12):2299-2307. doi: 10.1007/s11255-018-2011-x. Epub 2018 Oct 16.

DOI:10.1007/s11255-018-2011-x
PMID:30328087
Abstract

Defective renal salt and water excretion, together with increased salt intake, frequently contributes to hypertension. Recent studies indicate that Ste20 family kinases, such as proline-alanine-rich Ste20-related kinase (SPAK) and oxidative stress-response protein 1 (OSR1), are regulators of cell volume, ion transport, and hypertension. The aim of this study was to investigate whether mammalian sterile 20-like protein kinase 3 (MST3), which is also a stress-regulated kinase, is involved in the development of hypertension. MST3 expression was compared in Wistar-Kyoto (WKY) and spontaneously hypertensive rat (SHR) kidneys. MST3 expression was markedly reduced in principal cells of the collecting ducts from the renal inner medulla of SHR. The downregulation of MST3 expression was observed before and after the onset of hypertension in SHR. Mice fed high-salt diets (HS) exhibited a significant increase in MST3 protein level. This is the first study reporting that MST3, a Ste20-like kinase, exerts a conserved regulatory role in sodium homeostasis after high-salt diet and in the development of hypertension.

摘要

肾脏排盐排水功能缺陷,加上盐摄入量增加,常常会导致高血压。最近的研究表明,Ste20家族激酶,如富含脯氨酸-丙氨酸的Ste20相关激酶(SPAK)和氧化应激反应蛋白1(OSR1),是细胞体积、离子转运和高血压的调节因子。本研究的目的是调查同样作为应激调节激酶的哺乳动物无菌20样蛋白激酶3(MST3)是否参与高血压的发生发展。比较了Wistar-Kyoto(WKY)大鼠和自发性高血压大鼠(SHR)肾脏中MST3的表达。在SHR肾内髓集合管的主细胞中,MST3表达明显降低。在SHR高血压发作之前和之后均观察到MST3表达下调。喂食高盐饮食(HS)的小鼠MST3蛋白水平显著升高。这是第一项报道MST3这种Ste20样激酶在高盐饮食后钠稳态及高血压发生发展中发挥保守调节作用的研究。

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本文引用的文献

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Impact of Angiotensin Type 1A Receptors in Principal Cells of the Collecting Duct on Blood Pressure and Hypertension.集合管主细胞中血管紧张素1A型受体对血压和高血压的影响。
Hypertension. 2016 Jun;67(6):1291-7. doi: 10.1161/HYPERTENSIONAHA.115.06987. Epub 2016 May 2.
2
High Salt Diet Affects Renal Sodium Excretion and ERRα Expression.高盐饮食影响肾脏钠排泄及雌激素相关受体α(ERRα)表达。
Int J Mol Sci. 2016 Apr 1;17(4):480. doi: 10.3390/ijms17040480.
3
Animal Models in Cardiovascular Research: Hypertension and Atherosclerosis.心血管研究中的动物模型:高血压与动脉粥样硬化
三维基质中的上皮极化需要 MST3 信号来调节 ZO-1 的位置。
PLoS One. 2023 May 8;18(5):e0285217. doi: 10.1371/journal.pone.0285217. eCollection 2023.
4
MST3 Involvement in Na and K Homeostasis with Increasing Dietary Potassium Intake.随着饮食中钾摄入量增加,MST3参与钠和钾的稳态调节。
Int J Mol Sci. 2021 Jan 20;22(3):999. doi: 10.3390/ijms22030999.
Biomed Res Int. 2015;2015:528757. doi: 10.1155/2015/528757. Epub 2015 May 3.
4
Collecting duct principal cell transport processes and their regulation.集合管主细胞的转运过程及其调节。
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5
The WNK-regulated SPAK/OSR1 kinases directly phosphorylate and inhibit the K+-Cl- co-transporters.WNK 调节的 SPAK/OSR1 激酶可直接磷酸化并抑制 K+-Cl-共转运体。
Biochem J. 2014 Mar 15;458(3):559-73. doi: 10.1042/BJ20131478.
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Increased renal epithelial na channel expression and activity correlate with elevation of blood pressure in spontaneously hypertensive rats.自发性高血压大鼠血压升高与肾上皮钠通道表达和活性增加相关。
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