Biochemistry Department, University at Buffalo School of Medicine and Biomedical Sciences, Buffalo, New York
Biochemistry Department, University at Buffalo School of Medicine and Biomedical Sciences, Buffalo, New York.
Am J Physiol Renal Physiol. 2014 Sep 1;307(5):F539-50. doi: 10.1152/ajprenal.00510.2013. Epub 2014 Jul 9.
The actions of prostaglandin E2 (PGE2) in the kidney are mediated by G protein-coupled E-prostanoid (EP) receptors, which affect renal growth and function. This report examines the role of EP receptors in mediating the effects of PGE2 on Madin-Darby canine kidney (MDCK) cell growth. The results indicate that activation of Gs-coupled EP2 and EP4 by PGE2 results in increased growth, while EP1 activation is growth inhibitory. Indeed, two EP1 antagonists (ONO-8711 and SC51089) stimulate, rather than inhibit, MDCK cell growth, an effect that is lost following an EP1 knockdown. Similar observations were made with M1 collecting duct and rabbit kidney proximal tubule cells. ONO-8711 even stimulates growth in the absence of exogenous PGE2, an effect that is prevented by ibuprofen (indicating a dependence upon endogenous PGE2). The involvement of Akt was indicated by the observation that 1) ONO-8711 and SC51089 increase Akt phosphorylation, and 2) MK2206, an Akt inhibitor, prevents the increased growth caused by ONO-8711. The involvement of the EGF receptor (EGFR) was indicated by 1) the increased phosphorylation of the EGFR caused by SC51089 and 2) the loss of the growth-stimulatory effect of ONO-8711 and SC51089 caused by the EGFR kinase inhibitor AG1478. The growth-stimulatory effect of ONO-8711 was lost following an EGFR knockdown, and transduction of MDCK cells with a dominant negative EGFR. These results support the hypothesis that 1) signaling via the EP1 receptor involves Akt as well as the EGFR, and 2), EP1 receptor pharmacology may be employed to prevent the aberrant growth associated with a number of renal diseases.
前列腺素 E2(PGE2)在肾脏中的作用是由 G 蛋白偶联的 E 前列腺素(EP)受体介导的,这些受体影响肾脏的生长和功能。本报告研究了 EP 受体在介导 PGE2 对 Madin-Darby 犬肾(MDCK)细胞生长的影响中的作用。结果表明,PGE2 激活 Gs 偶联的 EP2 和 EP4 导致细胞生长增加,而 EP1 激活则抑制细胞生长。事实上,两种 EP1 拮抗剂(ONO-8711 和 SC51089)刺激而非抑制 MDCK 细胞生长,这种作用在 EP1 敲低后丧失。在 M1 集合管和兔肾近端小管细胞中也观察到类似的现象。ONO-8711 甚至在没有外源性 PGE2 的情况下刺激生长,这种作用被布洛芬(表明依赖内源性 PGE2)所阻止。Akt 的参与是通过观察到 1)ONO-8711 和 SC51089 增加 Akt 磷酸化,以及 2)Akt 抑制剂 MK2206 阻止 ONO-8711 引起的生长增加而表明的。表皮生长因子受体(EGFR)的参与是通过 1)SC51089 引起的 EGFR 磷酸化增加,以及 2)EGFR 激酶抑制剂 AG1478 导致 ONO-8711 和 SC51089 失去生长刺激作用而表明的。EGFR 敲低后,ONO-8711 的生长刺激作用丧失,而 MDCK 细胞转导显性负 EGFR。这些结果支持以下假设:1)通过 EP1 受体的信号转导涉及 Akt 以及 EGFR,以及 2)EP1 受体药理学可用于预防与许多肾脏疾病相关的异常生长。