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作 者:单智焱[1] 武玢 张玥[1] 薛媛[1] 吴嫣爽[1] 沈星辉[1] 雷蕾[1] 刘忠华[2]
机构地区:[1]哈尔滨医科大学组织学与胚胎学教研室,哈尔滨150081 [2]东北农业大学生命科学院,哈尔滨150081
出 处:《解剖学报》2015年第4期553-557,共5页Acta Anatomica Sinica
基 金:国家自然科学基金资助项目(C120115)
摘 要:目的通过诱导多能干细胞(i PSCs)技术重编程孤雌胚胎干细胞,探讨i PSCs技术对孤雌胚胎干细胞的多能性及印记基因的影响。方法从孤雌激活的囊胚中建立了孤雌胚胎干细胞;利用反转录病毒将多能性转录因子转入孤雌胚胎干细胞中,建立孤雌i PS细胞。结果建立的孤雌来源的i PS细胞体内外分化能力与孤雌胚胎干细胞的差别无显著性;Real-time PCR结果显示,孤雌i PS细胞母源印记基因的表达明显高于孤雌胚胎干细胞,父源印记基因表达下降,多能性基因表达升高。结论 i PSCs技术能影响基因的表达,尤其是印记基因,印记使其更接近于正常受精来源的胚胎干细胞中印记基因水平。Objective To investigate the effect of pluripotency and the expression of imprinted genes on the parthenogenetic embryonic stem cells( Pg ESCs) by induced pluripotent stem cells( i PSCs) reprogrmming. Methods In our study,we firstly generated the Pg ESCs from parthenogenetic blastocyst,induced the pluripotent factors into the Pg ESCs by retrovirus transfection and generated the i PS cells derived from Pg ESCs. Results It showed no difference in pluripotency and differentiation between Pg ESCs and Pg ESC-i PS cells,however,the expression of maternal imprinted genes was significantly increased and the expression of paternal imprinted genes was decreased in Pg ESC-i PS cells compared to that in Pg ESCs. Conclusion These results demonstrated the expression of imprinted genes could be modified by i PSCs reprogramming,which may be close to the expression level of imprinted genes in fertilized embronic stem cells.
关 键 词:孤雌胚胎干细胞 诱导多能干细胞 印记基因 实时定量聚合酶链反应 小鼠
分 类 号:R329.1[医药卫生—人体解剖和组织胚胎学]
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