ISSN 1004-6879

CN 13-1154/R

 

承德医学院学报 ›› 2025, Vol. 42 ›› Issue (5): 378-383.

• 临床医学 • 上一篇    下一篇

Smurf2靶向EYA2对高糖诱导肾小球系膜细胞增殖和纤维化的影响

陈丽贞1, 刘垠浩1,*, 陈育青2, 刘霏1, 郭腾捷3   

  1. 1.福建省漳州市中医院糖肾科,福建 漳州 363000;
    2.漳州卫生职业学院药学院,福建 漳州 363000;
    3.福建省漳州市中医院检验科,福建 漳州 363000
  • 收稿日期:2025-03-10 出版日期:2025-10-10 发布日期:2025-10-23
  • 通讯作者: *
  • 基金资助:
    漳州市自然科学基金(ZZ2023J09); 福建省自然科学基金(2024J011586)

Effect of Smurf2 Targeting EYA2 on Proliferation and Fibrosis of Glomerular Mesangial Cells Induced by High Glucose

CHEN Li-zhen1, LIU Yin-hao1,*, CHEN Yu-qing2, LIU Fei1, GUO Teng-jie3   

  1. 1. Department of Diabetes Nephrology Zhangzhou Hospital of Traditional Chinese Medicine, Fujian Zhangzhou 363000, China;
    2. School of Pharmacy Zhangzhou Health Vocational College, Zhangzhou, Fujian, 363000, China;
    3. Department of Clinical Laboratory Zhangzhou Hospital of Traditional Chinese Medicine, Zhangzhou, Fujian, 363000, China
  • Received:2025-03-10 Online:2025-10-10 Published:2025-10-23

摘要: 目的 探究Smurf2通过靶向EYA2影响高糖诱导肾小球系膜细胞增殖和纤维化的分子机制。方法 培养小鼠肾小球系膜细胞(GMCs),将sh-Smurf2与sh-NC载体转染到高糖诱导的GMCs中,分组为:空白对照组(NG)、高糖处理组(HG)、高糖+sh-NC组(HG+sh-NC)、高糖+sh-Smurf2组(HG+sh-Smurf2)。CCK-8实验和EdU实验检测各组细胞增殖,蛋白印迹法(Western blot)检测各组细胞Fibronectin、Collagen I、α-SMA蛋白的表达;采用CO-IP实验检测Smurf2与EYA2的靶向互作关系,进一步采用sh-EYA2与sh-NC载体转染GMCs中进行回溯实验验证。结果 与NG组相比,HG组细胞增殖显著上升,Fibronectin、Collagen I、α-SMA蛋白表达显著升高;与HG组相比,干扰Smurf2可以抑制细胞增殖,并抑制Fibronectin、Collagen I、α-SMA蛋白的表达。CO-IP结果显示Smurf2与EYA2存在靶向互作关系,且与HG+sh-Smurf2组相比,干扰EYA2可以促进细胞增殖,并促进Fibronectin、Collagen I、α-SMA蛋白的表达。结论 干扰Smurf2可以通过上调EYA2抑制高糖诱导的GMCs过度增殖与纤维化。

关键词: 肾小球系膜细胞, Smurf2, EYA2, 增殖, 纤维化

Abstract: Objective To explore the molecular mechanism of Smurf2's effect on hyperglycemia-induced mesangial cell proliferation and fibrosis by targeting EYA2. Methods Mouse mesangial cells (GMCs) were cultured, and sh-Smurf2 and sh-NC vectors were transfected into GMCs induced by high glucose. Cell proliferation in blank control group (NG), high glucose treatment group (HG), high glucose + sh-NC group (HG + sh-NC), and high glucose + sh-Smurf2 group (HG + sh-Smurf2) were detected by CCK-8 and EdU. The expressions of Fibronectin, Collagen I and α-SMA proteins were detected by Western blot. CO-IP assay was employed to detect the targeting interaction between Smurf2 and EYA2, and then sh-EYA2 and sh-NC vectors were used to transfect GMCs for backtracking experiments. Results Compared with NG group, cell proliferation and protein expression of Fibronectin, Collagen I and α-SMA in HG group were significantly increased. Compared with HG group, interference with Smurf2 inhibited cell proliferation and the expression of Fibronectin, Collagen I and α-SMA proteins. CO-IP results showed a targeted interaction between Smurf2 and EYA2. Compared with HG + sh-Smurf2 group, interference with EYA2 promoted cell proliferation and the expression of Fibronectin, Collagen I and α-SMA proteins. Conclusion Interference with Smurf2 can inhibit hyperproliferation and fibrosis of GMCs induced by high glucose by upregulating EYA2.

Key words: glomerular mesangial cells, Smurf2, EYA2, proliferation, fibrosis

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