【2h】

Rho GAPs and GEFs

机译:Rho GAP和GEF

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摘要

Within blood vessels, endothelial cell–cell and cell–matrix adhesions are crucial to preserve barrier function, and these adhesions are tightly controlled during vascular development, angiogenesis, and transendothelial migration of inflammatory cells. Endothelial cellular signaling that occurs via the family of Rho GTPases coordinates these cell adhesion structures through cytoskeletal remodelling. In turn, Rho GTPases are regulated by GTPase-activating proteins (GAPs) and guanine nucleotide exchange factors (GEFs). To understand how endothelial cells initiate changes in the activity of Rho GTPases, and thereby regulate cell adhesion, we will discuss the role of Rho GAPs and GEFs in vascular biology. Many potentially important Rho regulators have not been studied in detail in endothelial cells. We therefore will first overview which GAPs and GEFs are highly expressed in endothelium, based on comparative gene expression analysis of human endothelial cells compared with other tissue cell types. Subsequently, we discuss the relevance of Rho GAPs and GEFs for endothelial cell adhesion in vascular homeostasis and disease.
机译:在血管内,内皮细胞-细胞和细胞-基质的粘附对于维持屏障功能至关重要,并且在血管发育,血管生成和炎性细胞的跨内皮迁移过程中,这些粘附受到严格控制。通过Rho GTPases家族发生的内皮细胞信号传导通过细胞骨架重塑来协调这些细胞粘附结构。反过来,Rho GTPases受GTPase激活蛋白(GAP)和鸟嘌呤核苷酸交换因子(GEF)调控。为了了解内皮细胞如何引发Rho GTPases活性的变化,从而调节细胞粘附,我们将讨论Rho GAP和GEF在血管生物学中的作用。许多潜在重要的Rho调节剂尚未在内皮细胞中进行详细研究。因此,基于人类内皮细胞与其他组织细胞类型的比较基因表达分析,我们将首先概述哪些GAP和GEF在内皮中高度表达。随后,我们讨论了Rho GAP和GEF对血管稳态和疾病中内皮细胞粘附的相关性。

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