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在内皮素A受体缺乏信号传导的情况下,它会经历激动剂和拮抗剂介导的内化过程。

The endothelin subtype A receptor undergoes agonist- and antagonist-mediated internalization in the absence of signaling.

作者信息

Bhowmick N, Narayan P, Puett D

机构信息

Department of Biochemistry and Molecular Biology, University of Georgia, Athens 30602-7229, USA.

出版信息

Endocrinology. 1998 Jul;139(7):3185-92. doi: 10.1210/endo.139.7.6105.

Abstract

The potent vasoconstrictor and mitogen to smooth muscle cells, endothelin-1 (ET-1), acts via two distinct G protein-coupled receptors, subtype A (ETAR) and subtype B, that are coupled primarily to the Gq-phospholipase C signaling pathway. It is known that ET-1 binding to ETAR promotes internalization, with subsequent degradation of at least a portion of the bound ligand. To investigate whether signaling is required for endocytosis, we developed stably transfected lines of human embryonic kidney 293 cells expressing wild-type ETAR and a receptor chimera (ETARC) in which the C-terminal cytoplasmic tail to ETAR was replaced with that of the lutropin receptor, another G protein-coupled receptor, but one which signals through the Gs-adenylyl cyclase pathway. ETARC binds ET-1 like ETAR, but is deficient in signaling. Using a combined concanavalin A/sucrose gradient centrifugation technique to separate plasma membranes from other cellular membranes, we found that [125I]ET-1 is rapidly internalized into ETAR-expressing cells at 37 C (t1/2 for internalization = 5 min; endocytic rate constant = 0.1 min(-1); ETARC-expressing cells also internalize [125I]ET-1, albeit at a somewhat slower rate than wild-type receptor (t1/2 for internalization = 15 min; endocytic rate constant = 0.03 min(-1). Using immunofluorescence confocal microscopy and an antibody developed to the N-terminal region of ETAR, qualitatively similar results were obtained. In addition, it was found using confocal microscopy that the ETAR-selective antagonist, BQ123, also promoted rapid internalization in cells expressing ETAR. These results establish that inositol 1,4,5-trisphosphate signaling is not required for ligand-mediated internalization of ETAR and suggest that a receptor conformational change is necessary. Moreover, the finding that BQ123 promotes ETAR internalization is novel and has potentially important implications in its clinical use.

摘要

内皮素 -1(ET-1)是一种对平滑肌细胞具有强大作用的血管收缩剂和促细胞分裂剂,它通过两种不同的G蛋白偶联受体发挥作用,即A型亚型(ETAR)和B型亚型,这两种受体主要与Gq - 磷脂酶C信号通路偶联。已知ET-1与ETAR结合会促进内化,随后至少一部分结合的配体被降解。为了研究内吞作用是否需要信号传导,我们构建了稳定转染的人胚肾293细胞系,这些细胞表达野生型ETAR和一种受体嵌合体(ETARC),在ETARC中,ETAR的C末端细胞质尾巴被促黄体生成素受体(另一种G蛋白偶联受体)的C末端细胞质尾巴所取代,但促黄体生成素受体是通过Gs - 腺苷酸环化酶途径进行信号传导的。ETARC与ETAR一样能结合ET-1,但缺乏信号传导能力。我们使用伴刀豆球蛋白A/蔗糖梯度离心技术将质膜与其他细胞膜分离,发现[125I]ET-1在37℃时能迅速内化到表达ETAR的细胞中(内化的半衰期 = 5分钟;内吞速率常数 = 0.1分钟-1);表达ETARC的细胞也能内化[125I]ET-1,尽管其内化速率比野生型受体稍慢(内化的半衰期 = 15分钟;内吞速率常数 = 0.03分钟-1)。使用免疫荧光共聚焦显微镜和针对ETAR N末端区域开发的抗体,也获得了定性相似的结果。此外,通过共聚焦显微镜发现,ETAR选择性拮抗剂BQ123也能促进表达ETAR的细胞中的快速内化。这些结果表明,肌醇1,4,5 - 三磷酸信号传导对于ETAR的配体介导的内化不是必需的,提示受体构象变化是必要的。此外,BQ123促进ETAR内化这一发现是新颖的,并且在其临床应用中可能具有重要意义。

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