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作 者:俞晓丽[1,2] 王宁[1] 马洋洋[1] 万千惠 秦明鸣 王华岩[1]
机构地区:[1]西北农林科技大学动物医学院陕西省干细胞工程技术研究中心,陕西杨凌712100 [2]宁夏医科大学人体解剖学与组织胚胎学系生育力保持教育部重点实验室宁夏生殖与遗传重点实验室,宁夏银川750004
出 处:《生物工程学报》2015年第3期394-402,共9页Chinese Journal of Biotechnology
基 金:国家自然科学基金(No.31371505);宁夏医科大学校级项目(XT201412)资助~~
摘 要:干细胞通过诱导培养,在体外能够分化为卵母细胞样细胞(Oocyte-like cell,OLC),将其置于体内环境能够有效地改善OLC的质量和发育能力。通过检测猪卵泡液中激素和Bmp 15蛋白的含量,选取了中等卵泡的卵泡液对人羊水干细胞进行体外诱导培养,10 d后,经实时定量PCR检测发现,早期生殖细胞样细胞团高表达生殖基因oct4和重新甲基化转移酶基因dnmt3b。将这些细胞团用猪卵泡膜包裹后形成移植物,移植到小鼠肾被膜下。1个月后取出移植物,发现移植物内的细胞在形态上,不仅与正常的卵母细胞极为相似,而且还表达生殖细胞和卵母细胞特异标记基因(oct4、nanog、stella、ifitm3、dazl、nanos3、bmp15和gdf9)。证明技术体系能够有效改善OLC的形成和发育能力。Oocyte-like cells(OLC) can be generated by stem cells after the induction and differentiation in vitro, and maturated when transplanted in vivo to improve the development potential. Human amniotic fluid stem cells(h AFSC) were cultured for 10 days in porcine follicle fluid(p FF) that was extracted from the medium follicle with high levels of hormones and Bmp 15 protein. After the induction, the cell aggregates showed the germ cell-like cells and produced the germ cell marker oct4, and triggered epigenetic changes with high expression of methylation transferase gene dnmt3 b. The cell aggregates were packaged into porcine theca folliculi to form grafts, which were then transplanted into mouse renal capsule. After one month of transplantation, the morphology of OLC from a graft was not only similar to oocytes, but also expressed the germ cells markers(oct4, nanog, stella, ifitm3, dazl, nanos3, bmp15, and gdf9). The results demonstrate that the in vivo differentiation model was useful for OLC development.
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