摘要
目的探讨组蛋白去乙酰化酶抑制剂曲古抑菌素A(TSA)对组蛋白H3乙酰化水平的影响,进而提高他们重编程的能力。方法用不同浓度的TSA处理胎儿成纤维细胞,应用免疫荧光和WesternBlot方法对细胞乙酰化水平进行量化分析。结果0.5nM,5nM,50nM和100nM浓度的TSA均引起供体成纤维细胞形态学的变化,对供体成纤维细胞组蛋白H3乙酰化有明显的剂量效应,随着TSA浓度增加,组蛋白H3乙酰化水平逐渐增加,在TSA浓度5nM时比0.5nM增加尤为明显。结论TSA能够提高胎儿成纤维细胞组蛋白H3乙酰化水平,提高核移植重编程的能力。
Objective To study the effect of trichostatin A ( TSA ) upon histone H3 acetylation in nuclear transplantation ( NT ) donor cells, and improve their reprogramming. Method Mouse embryonic fibroblasts ( MEF ) were cultured and treated by different concentrations of TSA and MEF histone H3 acetylation was analysed using immunofluorescence and Western blot. Result TSA can significantly improve the histonc H3 acetylation in donor fibroblasts, the level of histone H3 acetylation increased as the increase of TSA concentrations, TSA with the different concentrations of 0.5UM, 5nM, 50nM and 100nM can alter donor cell morphology. Conclusion TSA promotes histone H3 acetylation and NT reprogramming capacity in MEF.
出处
《解剖科学进展》
CAS
2009年第2期134-137,共4页
Progress of Anatomical Sciences
基金
黑龙江省科技厅基金(LC02C13)
教育部留学归国基金
哈尔滨市科委基金(2002AA9CS151-0-5)