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Modulation of Na+,K(+)-ATPase activity by a tyrosine phosphorylation process in rat proximal convoluted tubule.

机译:Na +,K(+)-ATPase活性通过大鼠近曲小管中的酪氨酸磷酸化过程进行调节。

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摘要

1. In the rat kidney proximal convoluted tubule, epidermal growth factor and insulin have been reported to stimulate Na+ reabsorption. Because most of the effects of these growth factors are mediated by a process of tyrosine phosphorylation and Na+,K(+)-ATPase drives Na+ reabsorption, the influence of tyrosine kinases and tyrosine phosphatases on Na+,K(+)-ATPase activity located in the proximal convoluted tubule was evaluated. 2. Activation of receptor tyrosine kinases by epidermal growth factor and insulin stimulated ouabain-sensitive 86Rb+ uptake. The effects of epidermal growth factor and insulin were prevented by genistein, a tyrosine kinase inhibitor, but were unaffected by GF109203X, a protein kinase C inhibitor. 3. Inhibition of tyrosine phosphatases by orthovanadate (10(-7) and 10(-6)M) mimicked the effects of activation of receptor tyrosine kinases: stimulation of the ouabain-sensitive 86Rb+ uptake and of the hydrolytic activity of Na+,K(+)-ATPase under rate-limiting Na+ concentration, and absence of modification of the maximal activity (Vmax) of the enzyme. The effects of orthovanadate and insulin on the ouabain-sensitive 86Rb+ uptake were not additive. 4. The present results show that both activation of receptor tyrosine kinases and inhibition of tyrosine phosphatases stimulate the Na+,K(+)-ATPase activity through a common mechanism. Thus, a tyrosine phosphorylation process directly controls the Na+,K(+)-ATPase activity and contributes to the physiological control of water and solute reabsorption in the proximal convoluted tubule.
机译:1.据报道,在大鼠肾脏近曲小管中,表皮生长因子和胰岛素刺激了Na +重吸收。由于这些生长因子的大多数作用是由酪氨酸磷酸化过程介导的,而Na +,K(+)-ATPase驱动Na +重吸收,因此酪氨酸激酶和酪氨酸磷酸酶对位于评估近端曲折小管。 2.表皮生长因子和胰岛素刺激的哇巴因敏感性86Rb +摄取激活受体酪氨酸激酶。酪氨酸激酶抑制剂染料木黄酮可阻止表皮生长因子和胰岛素的作用,而蛋白激酶C抑制剂GF109203X则不影响表皮生长因子和胰岛素的作用。 3.原钒酸盐(10(-7)和10(-6)M)对酪氨酸磷酸酶的抑制作用模仿了受体酪氨酸激酶的激活作用:刺激了哇巴因敏感的86Rb +吸收和Na +,K( +)-ATPase在限速Na +浓度下,且没有修饰该酶的最大活性(Vmax)。原钒酸盐和胰岛素对哇巴因敏感的86Rb +吸收的影响不是累加的。 4.本结果表明,受体酪氨酸激酶的激活和酪氨酸磷酸酶的抑制均通过共同机制刺激Na​​ +,K(+)-ATPase活性。因此,酪氨酸磷酸化过程直接控制Na +,K(+)-ATPase的活性,并有助于生理控制水和溶质在近曲小管中的重吸收。

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