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大鼠肾血栓素受体:分子克隆、信号转导及肾内表达定位

Rat kidney thromboxane receptor: molecular cloning, signal transduction, and intrarenal expression localization.

作者信息

Abe T, Takeuchi K, Takahashi N, Tsutsumi E, Taniyama Y, Abe K

机构信息

Second Department of Internal Medicine, Tohoku University School of Medicine, Sendai, Japan.

出版信息

J Clin Invest. 1995 Aug;96(2):657-64. doi: 10.1172/JCI118108.

Abstract

Thromboxane (TX) plays important roles in control of renal hemodynamics and water and electrolyte metabolism, and is involved in the pathophysiology of many renal diseases. The aim of the present study is to isolate a rat kidney cDNA encoding functional TX receptor, and to reveal its intrarenal expression localization. A clone (rTXR2) was isolated from a rat kidney cDNA library by a homology screening approach. rTXR2 was shown to encode the amino acid sequence containing seven transmembrane spanning domains representing rat (r) TX receptor. The membrane from COS-7 cells transiently transfected with rTXR2 cDNA was shown to be specifically bound by a thromboxane receptor antagonist, SQ29548. Either in Xenopus oocyte expression or in transfected COS-7 cells, rTX receptor was shown to be linked with Ca2+ messenger system. TX receptor-mediated increase in cytosolic Ca2+ was also observed in cultured glomerular mesangial cells. In situ hybridization showed that rTX receptor mRNA was detected in renal glomeruli, smooth muscle cells in renal arterioles, and transitional cell epithelium of renal pelvis. Reverse transcription linked to PCR applied to microdissected nephron segments indicated the presence of rTX receptor mRNA exclusively in the glomerulus. In conclusion, we have cloned a functional rat kidney TX receptor, which is expressed specifically in renal glomerulus, arterial smooth muscle cells, and transitional cell epithelium of renal pelvis. The present study will provide important insights into the etiology and pathophysiology of renal diseases with relation to TX metabolism.

摘要

血栓素(TX)在肾血流动力学以及水和电解质代谢的调控中发挥着重要作用,并参与多种肾脏疾病的病理生理学过程。本研究的目的是分离编码功能性TX受体的大鼠肾脏cDNA,并揭示其在肾脏内的表达定位。通过同源筛选方法从大鼠肾脏cDNA文库中分离出一个克隆(rTXR2)。rTXR2被证明编码包含七个跨膜结构域的氨基酸序列,代表大鼠(r)TX受体。用rTXR2 cDNA瞬时转染的COS-7细胞膜被证明能与血栓素受体拮抗剂SQ29548特异性结合。无论是在非洲爪蟾卵母细胞表达中还是在转染的COS-7细胞中,rTX受体都被证明与Ca2+信使系统相关联。在培养的肾小球系膜细胞中也观察到TX受体介导的胞质Ca2+增加。原位杂交显示在肾小球、肾小动脉平滑肌细胞和肾盂移行细胞上皮中检测到rTX受体mRNA。应用于显微切割的肾单位节段的逆转录聚合酶链反应表明rTX受体mRNA仅存在于肾小球中。总之,我们克隆了一个功能性大鼠肾脏TX受体,它特异性表达于肾小球、动脉平滑肌细胞和肾盂移行细胞上皮中。本研究将为与TX代谢相关的肾脏疾病的病因和病理生理学提供重要见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9e3/185246/2ff9bacc43ff/jcinvest00014-0014-a.jpg

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