基础医学与临床 ›› 2016, Vol. 36 ›› Issue (2): 151-155.

• 研究论文 • 上一篇    下一篇

EGFR在高糖诱导下人肾小管上皮细胞凋亡中的作用

吴海江1,邓新娜2,史永红1,杜春阳1,韦金英1,任蕴卓1,段惠军1   

  1. 1. 河北医科大学
    2. 河北省人民医院
  • 收稿日期:2015-06-08 修回日期:2015-11-11 出版日期:2016-02-05 发布日期:2016-01-21
  • 通讯作者: 段惠军 E-mail:duanhuijun999@163.com
  • 基金资助:
    PGC-1α在糖尿病肾病中的作用和机制研究;SIRT1对高糖刺激下肾小管上皮细胞HK-2影响及机制研究

Role of EGFR in high glucose-induced apoptosis of human renal proximal tubular epithelial cells

  • Received:2015-06-08 Revised:2015-11-11 Online:2016-02-05 Published:2016-01-21

摘要: 目的 观察EGFR信号通路对高糖诱导下人肾小管上皮细胞(HK-2)凋亡的影响和机制。方法 体外培养HK-2细胞, 将细胞分为4组:对照组、渗透压对照组、高糖组和高糖加EGFR抑制剂AG1478组。用Western blot检测p-EGFR、total EGFR、cleaved caspase-3、BAX、BCL-2及β-actin的蛋白表达,四唑盐比色法(MTT)检测细胞活性,流式细胞术检测细胞凋亡。结果 与对照组和渗透压对照组相比,高糖组HK-2细胞EGFR活性、cleaved caspase-3表达、BAX/BCL-2比值和内质网应激(ERS)明显升高,细胞活性降低(P<0.01)。EGFR抑制剂AG1478能够明显抑制高糖诱导的HK-2细胞EGFR活化和细胞凋亡(P<0.05),提高细胞活性(P<0.05),同时抑制内质网应激(P<0.05)。结论 抑制EGFR活性能够减少高糖诱导的HK-2细胞凋亡,这可能是通过减少内质网应激实现的。

关键词: 糖尿病肾病, HK-2细胞, EGFR, 凋亡, 内质网应激

Abstract: Objective To investigate the effect of EGFR signaling pathway in apoptosis of human renal proximal tubular epithelial cells (HK-2) under high concentration of glucose. Methods HK-2 cells were cultured in vitro and divided into 4 groups: normal glucose group, mannitol control group, high glucose group, high glucose plus EGFR inhibitor group. Western blot analysis was used to determine the expression of phosphorylated EGFR, total EGFR, cleaved caspase-3、BAX, BCL-2 and β-actin. MTT assay was used to detect the proliferation of cells. Apoptosis of HK-2 was also analyzed by flow cytometry. Results Compared with normal glucose group and mannitol control group, the number of cell apoptosis (cleaved caspase-3 expression and BAX/BCL-2 ratio), activity of EGFR and endoplasmic reticulum stress (ERS) are significantly increased in HK-2 cells in high glucose group (P<0. 01). Specific EGFR inhibition (AG1478) inhibited high glucose-induced HK-2 cell apoptosis(P<0.05), EGFR activation(P<0.05), endoplasmic reticulum stress(P<0.05). Conclusions Inhibition of EGFR activation may prevent high glucose-induced HK-2 cell apoptosis through decreasing endoplasmic reticulum stress.

Key words: diabetic nephropathy, HK-2 cell, EGFR, apoptosis, endoplasmic reticulum stress

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