基因敲除
上皮-间质转换
基因亚型
生物
成纤维细胞生长因子
细胞生物学
糖尿病肾病
免疫印迹
间充质干细胞
免疫荧光
癌症研究
过渡(遗传学)
肾
内分泌学
细胞培养
免疫学
生物化学
基因
遗传学
受体
抗体
作者
Yingying Luo,Danfang Deng,Lamei Lin,Yikun Zhou,Lan Wang,Xinrong Zou,Xiaoqin Wang
标识
DOI:10.1016/j.yexcr.2022.113355
摘要
The role of different isoforms of Fibroblast growth factor-2 (FGF2) in tubular epithelial-to-mesenchymal transition (EMT) in diabetic nephropathy remains unknown. We aimed to evaluate the role of FGF2 isoforms in the pathogenesis of EMT.Western blot and immunofluorescence were used to assess the expression of FGF2 isoforms in db/db mice and high glucose-stimulated HK2 cells. The effects of specific FGF2 isoforms on EMT were explored via overexpression or knockdown of the corresponding isoform in HK2 cells cultivated in high glucose.Expression of low molecular weight (LMW) FGF2 was up-regulated while high molecular weight (HMW) FGF2 was down-regulated in the kidney of db/db mice and HK2 cells cultured in high glucose that underwent EMT. Overexpression of the LMW FGF2 enhanced EMT changes, while overexpression of the HMW FGF2 attenuated EMT. Knockdown of HMW FGF2 in HK2 cells promoted the EMT process.The expression and function of LMW and HMW FGF2 differed in the process of EMT in tubular cells. LMW FGF2 contributed to EMT, while HMW FGF2 played a protective role in the EMT process.
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