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J Am Soc Nephrol. 2013 Jun;24(7):1053-62. doi: 10.1681/ASN.2012080839. Epub 2013 Apr 18.
2
Rapid nongenomic action of aldosterone on protein expressions of Hsp90( α and β ) and pc-Src in rat kidney.醛固酮对大鼠肾脏中 Hsp90(α 和 β)和 pc-Src 蛋白表达的快速非基因组作用。
Biomed Res Int. 2013;2013:346480. doi: 10.1155/2013/346480. Epub 2013 Jan 22.
3
EP1 disruption attenuates end-organ damage in a mouse model of hypertension.EP1 破坏可减轻高血压小鼠模型中的靶器官损伤。
Hypertension. 2012 Nov;60(5):1184-91. doi: 10.1161/HYPERTENSIONAHA.112.199026. Epub 2012 Sep 24.
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PI3K-PKB/Akt pathway.PI3K-PKB/Akt 通路。
Cold Spring Harb Perspect Biol. 2012 Sep 1;4(9):a011189. doi: 10.1101/cshperspect.a011189.
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Prostaglandin E(2) mediates proliferation and chloride secretion in ADPKD cystic renal epithelia.前列腺素 E(2)介导 ADPKD 囊肿性肾上皮细胞的增殖和氯离子分泌。
Am J Physiol Renal Physiol. 2012 Nov 15;303(10):F1425-34. doi: 10.1152/ajprenal.00010.2012. Epub 2012 Aug 29.
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Diabetes. 2012 Jul;61(7):1879-87. doi: 10.2337/db11-1396. Epub 2012 Apr 20.
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Prostaglandin E2 stimulates cystogenesis through EP4 receptor in IMCD-3 cells.前列腺素 E2 通过 IMCD-3 细胞中的 EP4 受体刺激囊泡生成。
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Epidermal growth factor-mediated proliferation and sodium transport in normal and PKD epithelial cells.表皮生长因子介导的正常及多囊肾病上皮细胞的增殖与钠转运
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Novel targets for the treatment of autosomal dominant polycystic kidney disease.治疗常染色体显性遗传性多囊肾病的新靶点。
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10
Regulation of renal proximal tubule Na-K-ATPase by prostaglandins.前列腺素对肾近端小管钠-钾-ATP 酶的调节。
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在 MDCK 细胞中,前列腺素 E2 EP1 受体的拮抗作用通过激活 Akt 和表皮生长因子受体来增加细胞生长。

Antagonism of the prostaglandin E2 EP1 receptor in MDCK cells increases growth through activation of Akt and the epidermal growth factor receptor.

机构信息

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.

出版信息

Am J Physiol Renal Physiol. 2014 Sep 1;307(5):F539-50. doi: 10.1152/ajprenal.00510.2013. Epub 2014 Jul 9.

DOI:10.1152/ajprenal.00510.2013
PMID:25007872
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4154115/
Abstract

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.

摘要

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。