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足细胞YAP缺失会降低足细胞黏附,并通过α3β1整合素加剧局灶节段性肾小球硬化的进展。

Podocyte YAP ablation decreases podocyte adhesion and exacerbates FSGS progression through α3β1 integrin.

作者信息

Shao Guangze, Xu Jitu, Hu Chencheng, Jia Wenyao, Xu Xitong, Gu Yue, Zhang Luming, Zheng Zhihuang, Zhong Jiayan, Zhu Siqi, Meng Shenghao, Zhao Zhonghua, Zhang Zhigang, Liu Jun, Xu Yanyong, Wu Huijuan

机构信息

Department of Pathology of School of Basic Medical Sciences, Fudan University, Kidney and Dialysis Institute of Shanghai, Shanghai, PR China.

School of Biological Sciences, College of Life Science, Northwest A&F University, Xianyang, PR China.

出版信息

J Pathol. 2025 Jan;265(1):84-98. doi: 10.1002/path.6370.

Abstract

Severe proteinuria in focal segmental glomerulosclerosis (FSGS) is closely associated with decreased adhesion, and subsequent loss, of podocytes. Yes-associated protein (YAP) is a key transcriptional coactivator that plays a significant role in maintaining cellular homeostasis. However, its role in podocyte adhesion and its specific mechanism in FSGS progression remain unclear. In this study, an adriamycin (ADR)-induced FSGS model was established using podocyte-specific Yap knockout (KO) mice and control mice. These mice were further treated with Pyrintegrin, an agonist of α3β1 integrin, or a vehicle. Additionally, an ADR-induced FSGS model was constructed using podocyte-specific Itga3 KO mice, which were subsequently treated with 1-oleoyl lysophosphatidic acid (LPA), a YAP activator, or a vehicle. Our findings demonstrated that YAP was positively correlated with podocyte adhesion. Podocyte-specific Yap KO mice exhibited reduced levels of α3β1 integrin and podocyte adhesion. Yap KO aggravated the ADR-induced reduction in α3β1 integrin and podocyte adhesion, resulting in significantly increased segmental or global glomerulosclerosis and proteinuria. Notably, treatment with a β1 integrin agonist partially ameliorated the decrease of podocyte adhesion and the worsening FSGS progression caused by Yap KO. Mechanistically, YAP was found to transcriptionally regulate α3- and β1 integrin via transcriptional enhanced associate domain 3 (TEAD3), with TEAD3 binding to the promoter region of Itga3. Furthermore, Itga3 KO or knockdown abolished the beneficial effects of YAP activation on podocyte adhesion and FSGS progression. In conclusion, our results demonstrate that YAP regulates podocyte adhesion and FSGS progression through its transcriptional regulation of α3β1 integrin via TEAD3. This suggests that the YAP-TEAD3-α3β1 integrin axis may serve as a promising therapeutic target for FSGS. © 2024 The Pathological Society of Great Britain and Ireland.

摘要

局灶节段性肾小球硬化(FSGS)中的严重蛋白尿与足细胞黏附减少及随后的丢失密切相关。Yes相关蛋白(YAP)是一种关键的转录共激活因子,在维持细胞稳态中发挥重要作用。然而,其在足细胞黏附中的作用及其在FSGS进展中的具体机制仍不清楚。在本研究中,使用足细胞特异性Yap基因敲除(KO)小鼠和对照小鼠建立了阿霉素(ADR)诱导的FSGS模型。这些小鼠进一步用α3β1整合素激动剂Pyrintegrin或赋形剂处理。此外, 使用足细胞特异性Itga3基因敲除小鼠构建了ADR诱导的FSGS模型,随后用YAP激活剂1-油酰溶血磷脂酸(LPA)或赋形剂处理。我们的研究结果表明,YAP与足细胞黏附呈正相关。足细胞特异性Yap基因敲除小鼠的α3β1整合素水平和足细胞黏附降低。Yap基因敲除加重了ADR诱导的α3β1整合素和足细胞黏附减少,导致节段性或全球性肾小球硬化和蛋白尿显著增加。值得注意的是,用β1整合素激动剂治疗可部分改善Yap基因敲除引起的足细胞黏附减少和FSGS进展恶化。机制上,发现YAP通过转录增强结合域3(TEAD3)转录调节α3和β1整合素,TEAD3与Itga3的启动子区域结合。此外,Itga3基因敲除或敲低消除了YAP激活对足细胞黏附和FSGS进展的有益作用。总之,我们的结果表明,YAP通过TEAD3对α3β1整合素的转录调节来调控足细胞黏附和FSGS进展。这表明YAP-TEAD3-α3β1整合素轴可能是FSGS的一个有前景的治疗靶点。© 2024年英国和爱尔兰病理学会。

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