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调节血管内皮细胞中血流依赖性信号通路的G蛋白偶联受体的鉴定与验证

Identification and validation of G protein-coupled receptors modulating flow-dependent signaling pathways in vascular endothelial cells.

作者信息

Qiu Dike, Xu Ke, Chung Namjin, Robbins Jennifer, Luo Robert, Lawrence Michael, He Aiqing, Yu Fei, Alt Andrew, Miller Michael M, Hangeland Jon, Feder John N, Seiffert Dietmar, Arey Brian J

机构信息

Research and Early Development, Bristol Myers Squibb Company, Princeton, NJ, United States.

出版信息

Front Mol Biosci. 2023 Jun 8;10:1198079. doi: 10.3389/fmolb.2023.1198079. eCollection 2023.

Abstract

Vascular endothelial cells are exposed to mechanical forces due to their presence at the interface between the vessel wall and flowing blood. The patterns of these mechanical forces (laminar vs. turbulent) regulate endothelial cell function and play an important role in determining endothelial phenotype and ultimately cardiovascular health. One of the key transcriptional mediators of the positive effects of laminar flow patterns on endothelial cell phenotype is the zinc-finger transcription factor, krüppel-like factor 2 (KLF2). Given its importance in maintaining a healthy endothelium, we sought to identify endothelial regulators of the KLF2 transcriptional program as potential new therapeutic approaches to treating cardiovascular disease. Using an approach that utilized both bioinformatics and targeted gene knockdown, we identified endothelial GPCRs capable of modulating KLF2 expression. Genetic screening using siRNAs directed to these GPCRs identified 12 potential GPCR targets that could modulate the KLF2 program, including a subset capable of regulating flow-induced KLF2 expression in primary endothelial cells. Among these targets, we describe the ability of several GPCRs (GPR116, SSTR3, GPR101, LGR4) to affect KLF2 transcriptional activation. We also identify these targets as potential validated targets for the development of novel treatments targeting the endothelium. Finally, we highlight the initiation of drug discovery efforts for LGR4 and report the identification of the first known synthetic ligands to this receptor as a proof-of-concept for pathway-directed phenotypic screening to identify novel drug targets.

摘要

血管内皮细胞因其位于血管壁与流动血液之间的界面而受到机械力作用。这些机械力的模式(层流与湍流)调节内皮细胞功能,并在决定内皮细胞表型以及最终的心血管健康方面发挥重要作用。层流模式对内皮细胞表型产生积极影响的关键转录调节因子之一是锌指转录因子——Krüppel样因子2(KLF2)。鉴于其在维持健康内皮中的重要性,我们试图鉴定KLF2转录程序的内皮调节因子,作为治疗心血管疾病的潜在新疗法。通过利用生物信息学和靶向基因敲低的方法,我们鉴定出了能够调节KLF2表达的内皮G蛋白偶联受体(GPCR)。使用针对这些GPCR的小干扰RNA(siRNA)进行基因筛选,确定了12个可能调节KLF2程序的潜在GPCR靶点,其中包括一部分能够调节原代内皮细胞中血流诱导的KLF2表达的靶点。在这些靶点中,我们描述了几种GPCR(GPR116、SSTR3、GPR101、LGR4)影响KLF2转录激活的能力。我们还将这些靶点确定为开发针对内皮的新型治疗方法的潜在有效靶点。最后,我们强调了针对LGR4开展药物发现工作的启动,并报告了首个已知的该受体合成配体的鉴定结果,作为通过通路导向的表型筛选来鉴定新型药物靶点的概念验证。

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