期刊文献+

TGF-β1和EGFP体外电转染兔骨髓间充质干细胞的实验研究

TGF-β1 and EGFP electropration on rabbit bone marrow derived mesenchymal stem cells in vitro
下载PDF
导出
摘要 目的通过电转染介导转化生长因子β1(TGF-β1)转染兔骨髓间充质干细胞(BMSCs),观察Ⅱ型胶原表达的情况。方法用全骨髓细胞贴壁培养法分离、培养兔BMSCs;诱导14 d后,免疫组化和Western blot法检测Ⅱ型胶原表达。结果 BMSCs CD90表达阳性,CD31表达阴性;成功转染TGF-β1至BMSCs;通过免疫组化及Western blot法检测TGF-β1组细胞内Ⅱ型胶原有较强的表达,与增强型绿色荧光蛋白(EGFP)组和空白对照组相比差异有统计学意义(P<0.05)。结论电转TGF-β1质粒至兔BMSCs,可以促进Ⅱ型胶原表达。 Objective To observe cases of type Ⅱ collagen expression after transforming growth factor-β1 (TGF-β1) infected in rabbit bone mesenchymal stem cells( BMSCs) by electropration. Methods BMSCs from rabbit were isolated and cultured. 14 days after induction, immunohistochemistry and Western blot methods type Ⅱ colla-gen were used to detect the expression of type Ⅱ collagen. Results CD90 was positive and CD31 was negative by flow cytometry;successfully transfected with TGF-β1 to the BMSCs,the strong expression of type Ⅱ collagen in TGF-β1 group cells was shown by Western blot and immunocy-tochemical stain, which was compared with empty plasmid group and the control group,and the difference was statistically significant(P 〈 0. 05). Conclusion TGF-β1 plasmid by electroporation to rabbit BMSCs can facilitate expression of collagen Ⅱ.
出处 《安徽医科大学学报》 CAS 北大核心 2015年第5期581-584,共4页 Acta Universitatis Medicinalis Anhui
基金 国家自然科学基金(编号:31260233)
关键词 TGF-Β1 骨髓间充质干细胞 电转染 Ⅱ型胶原 transforming growth factor beta 1 mesenchymal stem cells electropration collagen Ⅱ
  • 相关文献

参考文献6

二级参考文献168

  • 1Dong-ChangZhao,Jun-XiaLei,RuiChen,Wei-HuaYu,Xiu-MingZhang,Shu-NongLi,PengXiang.Bone marrow-derived mesenchymal stem cells protect against experimental liver fibrosis in rats[J].World Journal of Gastroenterology,2005,11(22):3431-3440. 被引量:71
  • 2王士彬,孙才新,姚陈果,米彦,熊兰,李成祥,胡丽娜.电穿孔技术的研究及应用进展[J].国外医学(生物医学工程分册),2005,28(6):370-373. 被引量:6
  • 3潘海涛,郑启新,郭晓东,刘勇.兔骨髓基质干细胞的分离培养和鉴定及转化生长因子β1的基因瞬时转染研究[J].医学研究生学报,2006,19(6):508-511. 被引量:9
  • 4Wang T. The 26S proteasome system in the signaling pathways of TGF-β superfamily. Front Biosci 2003; 8:d1109- d1127.
  • 5Xu J, Attisano L. Mutations in the tumor suppressors Smad2 and Smad4 inactivate transforming growth factor β signaling by targeting Smads to the ubiquitin-proteasome pathway. Proc Natl Acad Sci USA 2000; 97:4820-4825.
  • 6Moren A, Itoh S, Moustakas A, ten Dijke P, Heldin CH. Functional consequences of tumorigenic missense mutations in the amino-terminal domain of Smad4. Oncogene 2000; 19:4396-4404.
  • 7Suzuki A, Shibata T, Shimada Y, et al. Identification of SMURF1 as a possible target for 7q21.3-22.1 amplification detected in a pancreatic cancer cell line by in-house arraybased comparative genomic hybridization. Cancer Sci 2008; 99:986-994.
  • 8Fukuchi M, Fukai Y, Masuda N, et al. High-level expression of the Smad ubiquitin ligase Smurf2 correlates with poor prognosis in patients with esophageal squamous cell carcinoma. Cancer Res 2002; 62:7162-7165.
  • 9Chen C, Sun X, Guo P, et al. Ubiquitin E3 ligase WWP1 as an oncogenic factor in human prostate cancer. Oncogene 2007; 26:2386-2894.
  • 10Chen C, Zhou Z, Ross JS, Zhou W, Dong JT. The amplified WWP1 gene is a potential molecular target in breast cancer. Int J Cancer 2007; 121:80-87.

共引文献70

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部