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前列腺素 E2 通过 IMCD-3 细胞中的 EP4 受体刺激囊泡生成。

Prostaglandin E2 stimulates cystogenesis through EP4 receptor in IMCD-3 cells.

机构信息

Department of Pediatrics, Section of Nephrology, the University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, United States.

出版信息

Prostaglandins Other Lipid Mediat. 2012 May;98(1-2):11-6. doi: 10.1016/j.prostaglandins.2012.03.005. Epub 2012 Apr 6.

Abstract

Previously, we demonstrated that prostaglandin E(2) (PGE(2)) induced cAMP and cyst formation through PGE(2) receptor-2 (EP2) activity in human autosomal-dominant polycystic kidney disease (ADPKD) epithelial cells. In this study, we determined the role of EP2 and EP4 receptors in mediating PGE(2) stimulation of cAMP signaling and cystogenesis in mouse renal epithelial cells using the inner medullary collecting duct-3 (IMCD-3) cell line. In contrast to human ADPKD cells, using novel EP2 and EP4 antagonists, we found that IMCD-3 cells expressed functional EP4 but not EP2, which stimulated cAMP formation and led to cyst formation in 3D culture system. The involvement of EP4 receptors in IMCD-3 cells was further supported by the specific effect of EP4 siRNA that inhibited PGE(2)-induced cystogenesis. We also observed different cellular localization of EP2 or EP4 receptors in IMCD-3 transfected cells. Collectively, our results suggest an important role of different expression of EP2 or EP4 receptors in the regulation of cystogenesis.

摘要

先前,我们证明前列腺素 E2(PGE2)通过人常染色体显性多囊肾病(ADPKD)上皮细胞中的 PGE2 受体-2(EP2)活性诱导 cAMP 和囊泡形成。在这项研究中,我们使用内髓集合管-3(IMCD-3)细胞系确定了 EP2 和 EP4 受体在介导 PGE2 刺激 cAMP 信号和囊泡发生中的作用。与人类 ADPKD 细胞相反,使用新型 EP2 和 EP4 拮抗剂,我们发现 IMCD-3 细胞表达功能性 EP4 但不表达 EP2,EP4 刺激 cAMP 形成并导致 3D 培养系统中的囊泡形成。EP4 受体在 IMCD-3 细胞中的参与还得到了 EP4 siRNA 的特异性作用的支持,该作用抑制了 PGE2 诱导的囊泡发生。我们还观察到转染的 IMCD-3 细胞中 EP2 或 EP4 受体的不同细胞定位。总之,我们的结果表明不同表达的 EP2 或 EP4 受体在调节囊泡发生中起重要作用。

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