单个内皮细胞P2Y2受体脱敏。

Priscila Sanabria, Elizabeth Ross, Edgardo Ramirez, Katiria Colon, Millie Hernandez, Hector M Maldonado, Walter I Silva, Carlos A Jimenez-Rivera, Fernando A Gonzalez
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引用次数: 7

摘要

受体脱敏,或受体对激动剂刺激的反应性降低,是一种可能对细胞行为产生重大影响的调节过程。P2Y(2)是一种被细胞外核苷酸激活的g蛋白偶联受体,在包括血管内皮在内的许多组织中经历脱敏。来自多种血管床的内皮细胞通常暴露于受损细胞和活化血小板释放的细胞外核苷酸。本研究的目的是比较在牛视网膜内皮细胞(微血管内皮模型)和人脐静脉内皮细胞(大血管内皮模型)中观察到的P2Y(2)受体脱敏。采用fura-2微荧光法,通过观察单细胞中utp刺激的胞内游离Ca(2 +)的变化来监测P2Y(2)受体脱敏。两种内皮细胞模型在UTP刺激后均表现出P2Y(2)受体脱敏。然而,细胞在速率、对激动剂浓度的依赖性和最大脱敏百分比上存在差异。这些结果提示P2Y(2)受体脱敏的不同机制,内皮细胞胞外核苷酸活性的异质性取决于其血管床起源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
P2Y2 receptor desensitization on single endothelial cells.

Receptor desensitization, or decreased responsiveness of a receptor to agonist stimulation, represents a regulatory process with the potential to have a significant impact on cell behavior. P2Y(2), a G-protein-coupled receptor activated by extracellular nucleotides, undergoes desensitization at many tissues, including the vascular endothelium. Endothelial cells from a variety of vascular beds are normally exposed to extracellular nucleotides released from damaged cells and activated platelets. The purpose of the present study was to compare P2Y(2) receptor desensitization observed in endothelial cells derived from bovine retina, a model of microvascular endothelium, and human umbilical vein endothelial cells (HUVECs), a model of a large blood vessel endothelium. P2Y(2) receptor desensitization was monitored by following changes in UTP-stimulated intracellular free Ca(2 +) in single cells using fura-2 microfluorometry. Both endothelial cell models exhibited desensitization of the P2Y(2) receptor after stimulation with UTP. However, the cells differed in the rate, dependence on agonist concentration, and percentage of maximal desensitization. These results suggest differential mechanisms of P2Y(2) receptor desensitization and favors heterogeneity in extracellular nucleotide activity in endothelial cells according to its vascular bed origin.

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