G3BP1 Maintains Vascular Endothelial Barrier Integrity by Negatively Regulating the MYD88-ARNO-ARF6 Signaling Pathway

Bin Wen, Weiyue Sun, Haoran Wu, Yuxi He, Huiqiao Chen, Yuanhui Meng, Guofang Tang, Jinshun Zhu, Zhengwang Wen, Rongzhou Wu, Guowei Wu, Chunxiang Zhang, Maoping Chu
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Abstract

Objective: We investigated the role of the RNA-binding protein G3BP1 in regulating endothelial permeability. Approach and Results: We examined the effects of loss of G3bp1 in conditional knockout mice and primary human HUVEC cells. We analyzed endothelial barrier integrity and permeability, focusing on AJ and TJ expression, under both normal and LPS-induced inflammatory conditions. Loss of G3bp1 in vascular endothelial cells decreased AJ and TJ expression, compromised barrier integrity, and increased permeability. These effects were exacerbated under LPS-induced inflammatory conditions. Loss of g3bp1 also increased the expression of MYD88, ARNO, and ARF6, and enhanced ARF6 activity. Mechanistically, G3BP1 bound to and stabilized MYD88 mRNA, negatively regulating the MYD88-ARNO-ARF6 signaling pathway. Inhibiting this pathway by reducing MYD88 or ARF6 expression, or inhibiting ARNO activity, restored AJ/TJ expression and barrier function in G3BP1-deficient models. Conclusion: Our findings identify G3BP1 as a novel regulator of vascular endothelial permeability. G3BP1 acts by negatively regulating the MYD88-ARNO-ARF6 signaling pathway.
G3BP1 通过负调控 MYD88-ARNO-ARF6 信号通路维持血管内皮屏障完整性
目的:我们研究了 RNA 结合蛋白 G3BP1 在调节内皮通透性中的作用:我们研究了 RNA 结合蛋白 G3BP1 在调节内皮通透性中的作用。方法与结果:我们研究了条件性基因敲除小鼠和原代人类 HUVEC 细胞中 G3bp1 缺失的影响。我们分析了正常和 LPS 诱导的炎症条件下内皮屏障的完整性和通透性,重点是 AJ 和 TJ 的表达。血管内皮细胞中 G3bp1 的缺失降低了 AJ 和 TJ 的表达,损害了屏障的完整性并增加了通透性。在 LPS 诱导的炎症条件下,这些影响加剧。缺失 g3bp1 还会增加 MYD88、ARNO 和 ARF6 的表达,并增强 ARF6 的活性。从机制上讲,G3BP1 与 MYD88 mRNA 结合并使其稳定,从而负向调节 MYD88-ARNO-ARF6 信号通路。通过减少 MYD88 或 ARF6 的表达或抑制 ARNO 的活性来抑制这一途径,可恢复 G3BP1 缺陷模型中 AJ/TJ 的表达和屏障功能。结论我们的研究发现 G3BP1 是血管内皮通透性的新型调节因子。G3BP1 通过负向调节 MYD88-ARNO-ARF6 信号通路发挥作用。
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