Slfn1通过下调Cyclin D1抑制内皮祖细胞的黏附功能
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(1.贵州省人民医院心内科,贵州省贵阳市 550003;2.贵州省人民医院体检中心,贵州省贵阳市 550003)

作者简介:

况春燕,博士,副主任医师,贵州医科大学硕士研究生导师,研究方向为冠心病、血管损伤与修复,E-mail为xiaokcy@sina.com。张璐,医师,研究方向为冠心病、血管损伤与修复,E-mail为121981891@qq.com。吴强,博士,主任医师,研究方向为冠心病、血管损伤与修复,E-mail为413972183@qq.com。

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基金项目:

国家自然科学基金(81360034);贵州省科技厅-贵州省人民医院联合基金(黔科合LS字[2011]024号)


Slfn1 Reduces the Adhension of Endothelial Progenitor Cells by Decreasing CyclinD1
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1.Department of Cardiology, ;2.Medical Examination Center, The People’s Hospital of Guizhou Province, Guiyang, Guizhou 550003, China)

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    摘要:

    目的 探讨睡眠因子1(Slfn1)对内皮祖细胞(EPC)黏附功能的影响。方法 实验分为空白对照组(未给予任何处理的EPC,N-control组)、腺病毒阴性对照组(Ad-control组)、Slfn1腺病毒载体组(Ad-Slfn1组)、发夹状RNA阴性对照组(ShRNA-control组)、发夹状RNA Slfn1干扰组(ShRNA-Slfn1组)。分离培养大鼠骨髓源性EPC,用ShRNA-control质粒、Ad-Slfn1及相应的对照质粒分别转染EPC,采用Western blot检测细胞Slfn1 及Cyclin D1表达,将EPC接种在预先铺好纤维连接蛋白的培养板中,观察其黏附功能。用流式细胞仪检测细胞周期。结果 ShRNA-Slfn1组Slfn1蛋白的表达明显低于ShRNA-control组,Ad- Slfn1组Slfn1蛋白的表达明显高于Ad-control组,说明转染有效。用ShRNA-Slfn1减弱EPC Slfn1基因的表达明显增强EPC的黏附能力,过表达Slfn1基因则明显抑制EPC的黏附能力。细胞周期检查结果显示,降低 EPC Slfn1基因的表达,EPC的细胞周期进入到S期细胞明显增多,过表达Slfn1基因使EPC的细胞周期停止在G1期。Western blot检测结果发现,ShRNA-Slfn1组Cyclin D1的蛋白表达明显高于ShRNA-control组,而Ad-Slfn1组Cyclin D1的蛋白表达则明显低于Ad-control组。结论 Slfn1通过下游靶点Cyclin D1负性调控EPC的黏附功能。

    Abstract:

    Aim To evaluate the effect of Schlafen 1 (Slfn1) on the adhension of endothelial progenitor cells (EPC). Methods Ad-Slfn1, ShRNA-Slfn1, ShRNA-control and Ad-control were transfected into EPC respectively.Then EPC were plated on fibronectin-coated culture dishes, adherent cells were counted. The protein of Slfn1 and Cyclin D1 were examined by Western blot. EPC cell cycle was examined by flow cytometry analysis. Results On 48 h after transfected ShRNA-Slfn1, the expression of Slfn1 protein was decreased significantly compared to that in ShRNA-control group (P<0.05), the transfection of Ad-Slfn1 reversed these responses. Overexpression of Slfn1 suppressed the adhension of EPC; conversely, the silencing of Slfn1 using shRNA-Slfn1 increased the adhension of EPC. In addition, cell cycle was arrested G1 phase in Ad-Slfn1 group. Whereas the transfection of shRNA-Slfn1 reversed these responses. The expression of Cyclin D1 protein after transfection of shRNA-Slfn1 was increased clearly compared to that in ShRNA-control group (P<0.05), in contrast, overexpression of Slfn1 reversed these results. Cyclin D1 was involved in Slfn1-mediated EPC adhension. Conclusion Slfn1 reduced the adhension of EPC through Cyclin D1.

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况春燕,张璐,吴强,杨天和,舒金,张萍. Slfn1通过下调Cyclin D1抑制内皮祖细胞的黏附功能[J].中国动脉硬化杂志,2016,24(1):1~6.

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  • 收稿日期:2015-04-02
  • 最后修改日期:2015-07-29
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  • 在线发布日期: 2018-11-19