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胰岛素与人类有机阴离子转运蛋白 4 之间的机制联系。

The mechanistic links between insulin and human organic anion transporter 4.

机构信息

Department of Pharmaceutics, Rutgers, The State University of New Jersey, Piscataway, NJ, USA.

Department of Pharmaceutics, Rutgers, The State University of New Jersey, Piscataway, NJ, USA.

出版信息

Int J Pharm. 2019 Jan 30;555:165-174. doi: 10.1016/j.ijpharm.2018.11.040. Epub 2018 Nov 16.

Abstract

Human organic anion transporter 4 (hOAT4) belongs to a class of organic anion transporters that exert critical function in the secretion, absorption, and distribution of numerous drugs in the body, such as anti-viral drugs, anti-cancer therapeutics, antibiotics, antihypertensive medicine, and anti-inflammatory drugs. hOAT4 is richly existent in the kidney and placenta. We previously established that serum- and glucocorticoid-inducible kinases (sgk) stimulate hOAT4 expression and transport activity by abrogating the inhibitory effect of a ubiquitin ligase Nedd4-2. Insulin is one of the upstream signaling molecules for sgk. We therefore investigated the effect of insulin on hOAT4 function. We showed that insulin stimulated hOAT4 expression and transport activity, and the action of insulin was abolished in cells overexpressing Nedd4-2-specific siRNA to knockdown the endogenous Nedd4-2. We further showed that insulin phosphorylated serine 327 on Nedd4-2 and weakened the interaction between hOAT4 and Nedd4-2. Interestingly, in cells overexpressing sgk2, the stimulatory effect of insulin on hOAT4 was diminished. In addition, the stimulatory effect of insulin on hOAT4 was blocked by wortmannin and buparlisib, two PI3K inhibitors. In conclusion, our study demonstrated that insulin stimulates hOAT4 expression and transport activity by abrogating the inhibition effect of Nedd4-2 on the transporter. Moreover, insulin regulates hOAT4 by competing with sgk2 rather than through sgk2.

摘要

人有机阴离子转运蛋白 4(hOAT4)属于有机阴离子转运蛋白家族,在体内许多药物的分泌、吸收和分布中发挥着关键作用,如抗病毒药物、抗癌疗法、抗生素、抗高血压药物和抗炎药物。hOAT4 在肾脏和胎盘丰富存在。我们之前的研究表明,血清和糖皮质激素诱导的激酶(sgk)通过消除泛素连接酶 Nedd4-2 的抑制作用来刺激 hOAT4 的表达和转运活性。胰岛素是 sgk 的上游信号分子之一。因此,我们研究了胰岛素对 hOAT4 功能的影响。我们表明,胰岛素刺激 hOAT4 的表达和转运活性,并且在过表达 Nedd4-2 特异性 siRNA 以敲低内源性 Nedd4-2 的细胞中,胰岛素的作用被消除。我们进一步表明,胰岛素使 Nedd4-2 的丝氨酸 327 磷酸化并削弱 hOAT4 与 Nedd4-2 之间的相互作用。有趣的是,在过表达 sgk2 的细胞中,胰岛素对 hOAT4 的刺激作用减弱。此外,胰岛素对 hOAT4 的刺激作用被两种 PI3K 抑制剂wortmannin 和 buparlisib 阻断。总之,我们的研究表明,胰岛素通过消除 Nedd4-2 对转运蛋白的抑制作用来刺激 hOAT4 的表达和转运活性。此外,胰岛素通过与 sgk2 竞争而不是通过 sgk2 来调节 hOAT4。

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