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兔肾单位中表皮生长因子结合位点的节段性分布

Segmental distribution of epidermal growth factor binding sites in rabbit nephron.

作者信息

Breyer M D, Redha R, Breyer J A

机构信息

Department of Medicine, Vanderbilt University, Nashville, Tennessee 37212.

出版信息

Am J Physiol. 1990 Oct;259(4 Pt 2):F553-8. doi: 10.1152/ajprenal.1990.259.4.F553.

Abstract

The kidney possesses epidermal growth factor (EGF) receptors and is a major site of synthesis for the EGF precursor, prepro-EGF. To examine the segmental localization of EGF receptors in the rabbit kidney, we characterized 125I-labeled EGF binding to micro-dissected rabbit nephron segments. Specific binding constituted 70-80% of total binding and was saturable with an apparent Kd of 8 nM. Kinetic studies (0 degrees C) revealed an association t1/2 of 20.7 min and a dissociation t1/2 of 27 min. Competition studies revealed that 125I-EGF binding was inhibited by unlabeled EGF or its homologue transforming growth factor-alpha, but not by parathyroid hormone or insulin. Mapping studies showed specific 125I-EGF binding (attomoles per centimeter) was highest in proximal straight tubules, followed by proximal convoluted tubules, cortical collecting ducts, inner medullary collecting ducts, outer medullary collecting ducts, and distal convoluted tubules. Specific binding to glomeruli was also observed. Interestingly, no specific binding of 125I-EGF to thick ascending limbs, a site of EGF precursor synthesis, was observed. These studies suggest potential sites of action for EGF in the rabbit kidney.

摘要

肾脏含有表皮生长因子(EGF)受体,是EGF前体——前EGF原的主要合成部位。为了研究EGF受体在兔肾脏中的节段定位,我们对125I标记的EGF与显微解剖的兔肾单位节段的结合进行了表征。特异性结合占总结合量的70 - 80%,具有饱和性,表观解离常数(Kd)为8 nM。动力学研究(0℃)显示结合半衰期(t1/2)为20.7分钟,解离半衰期为27分钟。竞争研究表明,125I - EGF的结合受到未标记的EGF或其同源物转化生长因子 - α的抑制,但不受甲状旁腺激素或胰岛素的抑制。定位研究表明,特异性125I - EGF结合(每厘米阿托摩尔数)在近端直小管中最高,其次是近端曲小管、皮质集合管、内髓集合管、外髓集合管和远端曲小管。也观察到了与肾小球的特异性结合。有趣的是,未观察到125I - EGF与厚壁升支(EGF前体合成部位)的特异性结合。这些研究提示了EGF在兔肾脏中的潜在作用部位。

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