
浏览全部资源
扫码关注微信
纸质出版:2008
移动端阅览
吕智美,邓华聪,诸葛福媛,刘金波,陈丹燕,南静.AP-1活化在高糖诱导肾小管上皮细胞转分化中的作用[J].陆军军医大学学报(原第三军医大学学报),2008,30(22):2107-2110.
LU Zhi-mei,DENG Hua-cong,ZHUGE Fu-yuan,LIU Jin-bo,CHEN Dan-yan,NAN Jing.Effect of AP-1 on high glucose induced epithelial-mesenchymal-transition of human kidney proximal tubular epithelial cell[J].J Amry Med Univ (J Third Mil Med Univ),2008,30(22):2107-2110.
吕智美,邓华聪,诸葛福媛,刘金波,陈丹燕,南静.AP-1活化在高糖诱导肾小管上皮细胞转分化中的作用[J].陆军军医大学学报(原第三军医大学学报),2008,30(22):2107-2110. DOI:
LU Zhi-mei,DENG Hua-cong,ZHUGE Fu-yuan,LIU Jin-bo,CHEN Dan-yan,NAN Jing.Effect of AP-1 on high glucose induced epithelial-mesenchymal-transition of human kidney proximal tubular epithelial cell[J].J Amry Med Univ (J Third Mil Med Univ),2008,30(22):2107-2110. DOI:
目的 探讨转录活化蛋白-1(activator protein-1
AP-1)在高糖诱导的肾小管上皮细胞表型转化中的作用。 方法 将体外培养的人肾小管上皮细胞(human kidney proximal tubular epithelial cell
HK2)分为正常对照组、高糖组、AP-1阻断组。光镜、透射电镜观察细胞形态的改变,免疫细胞化学法检测α-平滑肌肌动蛋白(α-SMA)和细胞角蛋白(cytokeratin,CK)的表达,用凝胶电泳迁移率改变分析法(electrophoretic mobility shift assay,EMSA)检测HK2细胞AP-1的改变,RT-PCR法检测CK mRNA的表达,Western blot检测α-SMA蛋白的表达。 结果 高糖作用48 h后,HK2细胞由椭圆形贴壁生长变为长梭形,胞体拉长,透射电镜下,细胞表面微绒毛明显减少,胞质内粗面内质网丰富,而AP-1阻断组较高糖组明显减轻;EMSA结果分析表明,在高糖刺激下,AP-1结合活力较正常对照组增加79.22%(P0.05),而AP-1阻断剂可明显抑制AP-1的活化,较高糖组降低51.19%(P0.05);免疫细胞化学和RT-PCR检测显示,高糖组和AP-1阻断组CK mRNA和蛋白水平明显降低(P0.05),而AP-1阻断组显著高于高糖组(P0.05);免疫细胞化学和Western blot检测显示,高糖组和AP-1阻断组α-SMA蛋白表达明显高于正常组(P0.05),而AP-1阻断组显著低于高糖组(P0.05)。 结论 高糖能够导致肾小管上皮细胞AP-1活化,诱导其表型转化。
Objective To examine the effect of AP-1 on high glucose induced epithelial-mesenchymal-transition in cultured human kidney proximal tubular epithelial cell (HK2). Methods The cultured HK2 cells were divided into three groups: normal glucose group (NG)
high glucose group (HG)
activator protein-1 (AP-1) inhibited group (AG). The morphological changes of HK2 cells were observed by inverted microscope and electron microscope. The proteins of α-smooth muscle actin (α-SMA) and cytokeratin (CK) were determined by immunocytochemistry. The activity of activator protein-1 (AP-1) was assessed with electrophoretic mobility shift assay (EMSA). RT-PCR was used to detect the mRNA expression of CK. Western blot was used to detect the protein expression of α-SMA. Results The HK2 cells stimulated with high glucose became elongated and the number of microvilli decreased
but the number of rough endoplasmic reticulum increased. The level of AP-1 binding activity was increased by 79.22% after high glucose treatment
compared with that of normal glucose group
but decreased by 51.19% after the treatment of AP-1 inhibitor
compared with that in high glucose group. Cultured with high glucose
the expressions of CK mRNA and protein significantly decreased (P0.05)
but they significantly increased in AP-1 inhibited group (P0.05). Upon the stimulation of high glucose
the expression of α-SMA protein increased markedly (P0.05)
while it significantly decreased in AP-1 inhibited group (P0.05). Conclusion High glucose induces transdifferentiation of renal tubular cells probably through the activation of AP-1.
0
浏览量
0
下载量
0
CSCD
关联资源
相关文章
相关作者
相关机构
京公网安备11010802024621