期刊文献+

miRlet7b在氧糖剥夺诱导原代大鼠增殖星形胶质细胞的表达

The expression of miRlet7b in the primary proliferated astrocytes of oxygen-glucose deprivation rat
原文传递
导出
摘要 目的研究miRlet7b在氧糖剥夺诱导原代Wistar大鼠增殖星形胶质细胞的表达,探讨缺氧缺血性脑损伤后星形胶质细胞增殖的分子机制。方法原代Wistar大鼠星形胶质细胞随机分为实验组(氧糖剥夺诱导的增殖组)和对照组(正常培养组)。EdU掺入法检测两组细胞的增殖,Western blot检测VEGF蛋白表达,real-time PCR方法检测两组细胞miRlet7b mRNA的表达。结果实验组EdU阳性细胞率,VEGF蛋白表达水平显著高于对照组(P<0.01),而实验组miRlet7b mRNA的表达水平显著低于对照组(P<0.01)。结论 MiRlet7b mRNA表达下调可能是缺氧缺血性脑损伤后星形胶质细胞增殖的分子机制之一,上调VEGF可能促进星形胶质细胞增殖。 Objective To study the expression and possible mechanism of miRlet7 b in the primary proliferated astrocytes of oxygen-glucose deprivation(OGD) rat.Methods The primary rat astrocytes were divided randomly into control group(normal culture group) and experimental group(proliferation group induced by OGD culture).The proliferation of primary rat astrocytes was measured by EdU incorporation,the expression of VEGF protein was detected by western blot,the expression of miRlet7 b was measured by real-time PCR.Results Edu positive ratio of primary astrocytes was significantly higher,the expression level of VEGF protein in the proliferated astrocytes was significantly increased in the experimental group than in control group(P〈0.01 or P〈0.05),but the expression level of miRlel7 b in the proliferated astrocytes was lower in the experimental group than in control group(P〈0.01).Conclusion The lower expression of miRlet7 b may be one of the molecular mechanisms in the proliferation of astrocytes,and upregulated VEGF possibly promotes the proliferation of astrocytes after hypoxic—ischemia brain injury.
出处 《解剖科学进展》 2016年第1期1-4,共4页 Progress of Anatomical Sciences
基金 国家自然科学基金(81501299)
关键词 星形胶质细胞 氧糖剥夺 miRlet7b VEGF WISTAR大鼠 astrocyte oxygen-glucose deprivation miRlet7b VEGF Wistar rat
  • 相关文献

参考文献4

二级参考文献69

  • 1邱瑾,姚文龙,张玥,邹姮婧,石小云,李大佳,张传汉.慢病毒过表达Cdh1蛋白对星形胶质细胞反应性增殖作用的初步研究[J].中风与神经疾病杂志,2012,29(2):100-102. 被引量:2
  • 2Barrel DP. MicroRNAs: genomics, biogenesis, mechanism, and function. Cell 2004; 116:281-297.
  • 3Esquela-Kerscher A, Slack FJ. Oncomirs - microRNAs with a role in cancer. Nat Rev Cancer 2006; 6:259-269.
  • 4Johnson SM, Grosshans H, Shingara J, et al. R.AS is regulated by the let-7 microRNA family. Cell 2005; 120:635-647.
  • 5Michael MZ, O'Connor SM, van Hoist Pellekaan NG, Young GP, James RJ. Reduced accumulation of specific microRNAs in colorectal neoplasia. Mol Cancer Res 2003; 1:882-891.
  • 6Iorio MV, Ferracin M, Liu CG, et al. MicroRNA gene expression deregulation in human breast cancer. Cancer Res 2005; 65:7065- 7070.
  • 7Volinia S, Calin GA, Liu CG, et al. A microRNA expression signature of human solid tumors defines cancer gene targets. Proc Natl Acad Sci USA 2006; 103:2257-2261.
  • 8Gaur A, Jewell DA, Liang Y, et al. Characterization ofmicroRNA expression levels and their biological correlates in human cancer cell lines. Cancer Res 2007; 67:2456-2468.
  • 9Lu J, Getz G, Miska EA, et al. MicroRNA expression profiles classify human cancers. Nature 2005; 435:834-838.
  • 10Zhang L, Huang J, Yang N, et al. microRNAs exhibit high frequency genomic alterations in human cancer. Proc Natl Acad Sci USA 2006; 103:9136-9141.

共引文献45

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