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埃兹蛋白通过 YAP 和 Akt 信号通路调节类风湿关节炎滑膜血管生成。

Ezrin regulates synovial angiogenesis in rheumatoid arthritis through YAP and Akt signalling.

机构信息

Department of Special Clinics, Stomatological Hospital, Southern Medical University, Guangzhou, Guangdong, China.

Department of Dermatology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China.

出版信息

J Cell Mol Med. 2021 Oct;25(19):9378-9389. doi: 10.1111/jcmm.16877. Epub 2021 Aug 29.

Abstract

This study aimed to investigate the role and regulatory mechanisms of Ezrin in synovial vessels in rheumatoid arthritis (RA). Synovial tissues were obtained from people with osteoarthritis people and patients with RA patients. We also used an antigen-induced arthritis (AIA) mice model by using Freund's adjuvant injections. Ezrin expression was analysed by immunofluorescence and immunohistochemical staining in synovial vessels of patients with RA and AIA mice. We investigated the role of Ezrin on vascular endothelial cells and its regulatory mechanism in vivo and in vitro by adenoviral transfection technology. Our results suggest a role for the Ezrin protein in proliferation, migration and angiogenesis of vascular endothelial cells in RA. We also demonstrate that Ezrin plays an important role in vascular endothelial cell migration and tube formation through regulation of the Hippo-yes-associated protein 1 (YAP) pathway. YAP, as a key protein, can further regulate the activity of PI3K/Akt signalling pathway in vascular endothelial cells. In AIA mice experiments, we observed that the inhibition of Ezrin or of its downstream YAP pathway can affect synovial angiogenesis and may lead to progression of RA. In conclusion, Ezrin plays an important role in angiogenesis in the RA synovium by regulating YAP nuclear translocation and interacting with the PI3K/Akt signalling pathway.

摘要

本研究旨在探讨 Ezrin 在类风湿关节炎 (RA) 滑膜血管中的作用及其调控机制。我们从骨关节炎患者和 RA 患者中获取滑膜组织,并使用弗氏完全佐剂注射建立抗原诱导性关节炎 (AIA) 小鼠模型。通过免疫荧光和免疫组织化学染色分析 RA 患者和 AIA 小鼠滑膜血管中的 Ezrin 表达。我们通过腺病毒转染技术,在体内和体外研究了 Ezrin 对血管内皮细胞的作用及其调控机制。研究结果表明 Ezrin 蛋白在 RA 血管内皮细胞的增殖、迁移和血管生成中发挥作用。我们还证明,Ezrin 通过调节 Hippo-YAP 相关蛋白 1(YAP)通路,在血管内皮细胞迁移和管状形成中发挥重要作用。YAP 作为关键蛋白,可以进一步调节血管内皮细胞中 PI3K/Akt 信号通路的活性。在 AIA 小鼠实验中,我们观察到 Ezrin 或其下游 YAP 通路的抑制可以影响滑膜血管生成,并可能导致 RA 进展。总之,Ezrin 通过调节 YAP 核转位并与 PI3K/Akt 信号通路相互作用,在 RA 滑膜血管生成中发挥重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dce7/8500952/059584ef3ef9/JCMM-25-9378-g005.jpg

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