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