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首页> 外文期刊>Stem Cell Studies >In vitro and in vivo lineage conversion of bone marrow stem cells into germ cells in experimental Azoospermia in rat
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In vitro and in vivo lineage conversion of bone marrow stem cells into germ cells in experimental Azoospermia in rat

机译:大鼠无精症大鼠骨髓干细胞体外和体内谱系转化为生殖细胞

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The present study is conducted to assess in vitro transdifferentiation of bone marrow derived mesenchymal stem cells (MSCs) into germ cells and in vivo transdifferentiation into spermatids and spermatocytes in the seminiferous tubules of azoospermic rats. Forty eight male rats were included in the study and were divided into: group 1; control rats, group 2; experimental azoospermic rats, group 3; azoospermic rats received undifferentiated MSCs. Group 4; azoospermic rats received transdifferentiated MSCs into germ cells. Quantitative real time PCR was conducted to assess gene expression of a primordial germ cell marker (VASA), stem cell specific markers (Oct4, SSEA-1 and SSEA-3), specific molecular markers of germ cells (c-Kit, Daz1); premeiotic marker (Daz1) and post-meiotic markers (c- Kit, Stra 8). Histopathological examination of rat testicular tissue was also conducted. Results revealed that 12 weeks after transplantation, fluorescent labeled MSCs were detected in the seminiferous tubules of the testes of group 3 and group 4 rats. In group 3 and 4, stem cell specific markers; Oct4, SSEA-1 and SSEA-3 were detected. In group 4, genes of primordial germ cell marker; VASA, premeiotic marker; Daz1and post-meiotic markers; c-Kit, Stra 8 were expressed. Daz1 was also expressed in group 3 rats to a significantly lower extent in comparison to group 4 rats. Spermatocytes and spermatids were detected in testicular tissue of group 4 rats. In conclusion, MSCs have potentials for in vitro transdifferentiation into germ cells and in vivo transdifferentiation into spermatids and spermatocytes.
机译:进行本研究以评估骨髓来源的间充质干细胞(MSCs)在体外的转分化为生殖细胞,以及在体内的体外转分化为无精子症大鼠的生精小管中的精子和精细胞。该研究包括48只雄性大鼠,并分为:第1组;和第1组。对照组,第2组;实验性无精子症大鼠,第3组;无精子症大鼠接受未分化的MSC。第4组;无精子症大鼠将转分化的MSC移植到生殖细胞中。进行实时定量PCR以评估原始生殖细胞标志物(VASA),干细胞特异性标志物(Oct4,SSEA-1和SSEA-3),生殖细胞特异性分子标志物(c-Kit,Daz1)的基因表达;减数分裂前标记(Daz1)和减数分裂后标记(c-Kit,Stra 8)。还对大鼠睾丸组织进行了组织病理学检查。结果显示,移植后12周,在第3组和第4组大鼠睾丸的生精小管中检测到荧光标记的MSC。在第3和第4组中,干细胞特异性标记; 10月4日,检测到SSEA-1和SSEA-3。第4组,原始生殖细胞标记基因; VASA,减数分裂前标记; Daz1和减数分裂后标记;表达了c-Kit,Stra 8。与第4组大鼠相比,Daz1在第3组大鼠中的表达也显着降低。在第4组大鼠的睾丸组织中检测到精细胞和精子。总之,MSC具有体外转分化为生殖细胞和体内转分化为精细胞和精细胞的潜力。

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