Characterization of dual agonists for kinin B1 and B2 receptors and their biased activation of B2 receptors

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• 作者：Xianming Zhang^a ; Jessica L. Lowry^a ; Viktor Brovkovych^a ; Randal A. Skidgel^a ; ^b ; ^{rskidgel@uic.edu}
• 关键词：CP ; carboxypeptidase ; kB1R ; kinin B1 receptor ; kB2R ; bradykinin B2 receptor ; [Ca2  ; +]i ; intracellular calcium concentration ; PBS ; phosphate buffered saline ; DMEM ; Dulbecco's Modified Eagle's Medium ; GPCR ; G protein-coupled receptor ; BK ; bradykinin ; KD
• 刊名：Cellular Signalling
• 出版年：2012
• 期刊代码：42_08986568
• 类别：bio
• 出版时间：August, 2012
• 卷：24
• 期：8
• 页码：1619-1631
• 文件大小：1314 K

摘要

Kinin B1 and B2 receptors (kB1R and kB2R) play important roles in many physiological and pathological processes. In some cases, kB1R or kB2R activation can have overlapping or complementary beneficial effects, thus an activator of both receptors might be advantageous. We found that replacement of the C-terminal Arg in the natural kB2R activators bradykinin (BK) or kallidin (KD) with Lys (K⁹-BK or K¹⁰-KD) resulted in agonists that effectively stimulate the downstream signaling of both the kB1R and kB2R as measured by increased inositol turnover, intracellular calcium, ERK1/2 phosphorylation, arachidonic acid release and NO production. However, K⁹-BK and K¹⁰-KD displayed some characteristics of biased agonism for kB2Rs as indicated by the rapid kinetics of ERK1/2 phosphorylation induced by K⁹-BK or K¹⁰-KD compared with the prolonged response mediated by BK or KD. In contrast, kinetics of ERK phosphorylation stimulated by K¹⁰-KD activation of the kB1R was the same as that induced by known kB1R agonist des-Arg¹⁰-KD. Furthermore, the endocytosis of kB2Rs mediated by K⁹-BK and K¹⁰-KD was remarkably less than that induced by BK and KD respectively. K¹⁰-KD stimulated kB1R and kB2R-dependent calcium responses and ERK1/2 phosphorylation in bovine endothelial cells. In cytokine-treated human endothelial cells, K¹⁰-KD stimulated ERK1/2 phosphorylation and a transient peak of NO production that was primarily kB2R-dependent. K¹⁰-KD also stimulated prolonged NO production that was both kB1R and kB2R-dependent. These data provide the first examples of dual agonists of kB1R and kB2R, and a biased agonist of kB2R and may provide useful clues for developing dual modulators of kB1Rs and kB2Rs for potential therapeutic use.