1. Signaling Pathways
  2. GPCR/G Protein
  3. GPR4

GPR4 (G蛋白偶联受体4)

G Protein-Coupled Receptor 4

GPR4是一种质子感应G蛋白偶联受体,在血管内皮细胞中高表达,是炎症反应的关键调节因子。酸中毒是炎症、缺血、肿瘤等多种病理状态的微环境标志,可激活GPR4。GPR4在多种病理状态下起促炎作用。酸中毒激活GPR4可刺激内皮细胞表达炎症趋化因子、细胞因子、粘附分子和NF-κB通路,增加内皮-白细胞粘附,促进白细胞浸润。此外,酸中毒激活GPR4可促进内质网应激反应和内皮细胞凋亡。此外,一些研究表明,GPR4可在酸性pH下促进血管生成,并能调节内皮细胞的管腔形成、迁移和增殖。GPR4 基因敲除小鼠的血管形态发生改变,血管长度和密度降低。

GPR4 is a proton-sensing G-protein-coupled receptor that is highly expressed in vascular endothelial cells. And GPR4 has emerged as a key regulator of inflammatory responses. GPR4 can be activated by acidosis which is a microenvironment hallmark of numerous pathological conditions such as inflammation, ischemia, and tumors. GPR4 plays a pro-inflammatory role in various pathological conditions. Activation of GPR4 by acidosis stimulates the expression of inflammatory chemokines, cytokines, adhesion molecules and the NF-κB pathway in endothelial cells, increases endothelium-leukocyte adhesion, and facilitates leukocyte infiltration. Moreover, activation of GPR4 by acidosis promotes the endoplasmic reticulum (ER) stress response and apoptosis of endothelial cells. In addition, some studies have demonstrated that GPR4 can promote angiogenesis at acidic pH and is capable of regulating the tube formation, migration, and proliferation of endothelial cells. GPR4 knockout mice displayed altered vessel morphology and reduced vascular length and density.

GPR4 相关产品 (2):

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-101784
    NE 52-QQ57 99.89%
    NE 52-QQ57 是选择性,有口服活性的 GPR4 拮抗剂,IC50为70 nM。NE 52-QQ57 具有抗炎活性。
    NE 52-QQ57
  • HY-101536
    GPR4 antagonist 1 Antagonist 98.92%
    GPR4 antagonist 1 是 GPR4 的拮抗剂,其 IC50 值为 189 nM。
    GPR4 antagonist 1