临床口腔医学杂志
臨床口腔醫學雜誌
림상구강의학잡지
JOURNAL OF CLINICAL STOMATOLOGY
2015年
4期
213-216
,共4页
付水霆%代天国%刘忠龙%金淑芳%何悦
付水霆%代天國%劉忠龍%金淑芳%何悅
부수정%대천국%류충룡%금숙방%하열
颌骨纤维化%骨髓间充质干细胞%肌成纤维细胞%TGF-β1%miRNA-21
頜骨纖維化%骨髓間充質榦細胞%肌成纖維細胞%TGF-β1%miRNA-21
합골섬유화%골수간충질간세포%기성섬유세포%TGF-β1%miRNA-21
Fibrosis of jaw%mesenchymal stem cells%myofibroblast%TGF-β1%miRNA-21
目的:在细胞水平探索miR-21在调控TGF-β1诱导的大鼠骨髓间充质干细胞向肌成纤维细胞分化中的作用。方法:全髓培养法培养原代大鼠骨髓间充质干细胞,培养至第三代时用TGF-β1分组诱导培养,检测TGF-β1对大鼠BMSCs促纤维化的作用及该过程中不同浓度梯度TGF-β1诱导以及不同时间段miR-21的表达变化;通过转染miR-21 mimics(高表达)不同时间点检测其对α-SMA表达的影响。结果:TGF-β1能促进大鼠骨髓间充质干细胞向成纤维,肌成纤维细胞分化;大鼠骨髓间充质干细胞向成纤维,肌成纤维细胞分化后miR-21表达上调;上调miR-21能促进大鼠BMSCs的纤维化作用。结论:miR-21 mimics能够促进大鼠BMSCs的纤维化作用。
目的:在細胞水平探索miR-21在調控TGF-β1誘導的大鼠骨髓間充質榦細胞嚮肌成纖維細胞分化中的作用。方法:全髓培養法培養原代大鼠骨髓間充質榦細胞,培養至第三代時用TGF-β1分組誘導培養,檢測TGF-β1對大鼠BMSCs促纖維化的作用及該過程中不同濃度梯度TGF-β1誘導以及不同時間段miR-21的錶達變化;通過轉染miR-21 mimics(高錶達)不同時間點檢測其對α-SMA錶達的影響。結果:TGF-β1能促進大鼠骨髓間充質榦細胞嚮成纖維,肌成纖維細胞分化;大鼠骨髓間充質榦細胞嚮成纖維,肌成纖維細胞分化後miR-21錶達上調;上調miR-21能促進大鼠BMSCs的纖維化作用。結論:miR-21 mimics能夠促進大鼠BMSCs的纖維化作用。
목적:재세포수평탐색miR-21재조공TGF-β1유도적대서골수간충질간세포향기성섬유세포분화중적작용。방법:전수배양법배양원대대서골수간충질간세포,배양지제삼대시용TGF-β1분조유도배양,검측TGF-β1대대서BMSCs촉섬유화적작용급해과정중불동농도제도TGF-β1유도이급불동시간단miR-21적표체변화;통과전염miR-21 mimics(고표체)불동시간점검측기대α-SMA표체적영향。결과:TGF-β1능촉진대서골수간충질간세포향성섬유,기성섬유세포분화;대서골수간충질간세포향성섬유,기성섬유세포분화후miR-21표체상조;상조miR-21능촉진대서BMSCs적섬유화작용。결론:miR-21 mimics능구촉진대서BMSCs적섬유화작용。
Objective:To investigate the role of miR-21 in the jaw of fibrosis in vitro. Method:Whole bone marrow adherence on plastic was used to isolation and culture rat mesenchymal stem cells. When passage 3, the cells were treated with TGF-β1 for different periods of time and concentration. The target gene expression of miR-21 was detected by real-time PCR;Over-expression of miR-21 by niR-21 mimics,to study whether up-regulated miR-21 enhances myfibroblast differentiation of rat mesenchymal stem cells by immunohistochemistry. Result:Real-time PCR demonstrated that TGF-β1 induced miR-21 expression in a time-dependent and dosage-dependent manner,peaking at 48h with an optimal dose at 5 ng/mL. The protein expression of α-SMA was up-regulated. Conclusion:miR-21 could promote myfibroblast differentia-tion of BMSCs in vitro. Inhibition of miR-21 may be a therapeutic approach to suppress renal fibrosis.