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Enrichment and In Vitro Culture of Spermatogonial Stem Cells from Pre-Pubertal Monkey Testes

机译:产前猴子睾丸精原干细胞的富集和体外培养

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摘要

Spermatogonial stem cells (SSCs) are essential for spermatogenesis throughout the lifespan of the male. However, the rarity of SSCs has raised the need for an efficient selection method, but little is known about culture conditions that stimulate monkey SSC proliferation in vitro. In this study, we report the development of effective enrichment techniques and in vitro culturing of germ cells from pre-pubertal monkey testes. Testis cells were analyzed by fluorescence-activated cell sorting techniques and were transplanted into the testes of nude mice to characterize SSCs. Thy-1-positive cells showed a higher number of colonies than the unselected control after xenotransplantation. Extensive colonization of monkey cells in the mouse testes indicated the presence of highly enriched populations of SSCs in the Thy-1-positive sorted cells. Furthermore, monkey testis cells were enriched by differential plating using extracellular matrix, laminin, and gelatin, and then cultured under various conditions. Isolation of monkey testicular germ cells by differential plating increased germ cell purity by 2.7-fold, following the combinational isolation method using gelatin and laminin. These enriched germ cells actively proliferated under culture conditions involving StemPro medium supplemented with bFGF, GDNF, LIF, and EGF at 37 °C. These results suggest that the enrichment and in vitro culture method proposed in the present study for harvesting a large number of functionally active monkey SSCs can be applied as the basis for efficient in vitro expansion of human SSCs.
机译:精原干细胞(SSCs)对于男性整个寿命中的精子发生必不可少。然而,SSC的稀有性提高了对一种有效选择方法的需求,但对体外刺激猴子SSC增殖的培养条件知之甚少。在这项研究中,我们报告了从青春期前睾丸睾丸生殖细胞的有效富集技术和体外培养的发展。通过荧光激活细胞分选技术分析睾丸细胞,并将其移植到裸鼠的睾丸中以表征SSC。异种移植后,Thy-1阳性细胞显示出比未选择的对照更高的菌落数量。小鼠睾丸中猴子细胞的广泛定殖表明在Thy-1阳性分选细胞中存在高度富集的SSC群体。此外,使用细胞外基质,层粘连蛋白和明胶通过差异平板富集猴睾丸细胞,然后在各种条件下培养。使用明胶和层粘连蛋白的组合分离方法后,通过差异平板分离法分离猴睾丸生殖细胞可使生殖细胞纯度提高2.7倍。这些富集的生殖细胞在涉及补充了bFGF,GDNF,LIF和EGF的StemPro培养基的培养条件下在37°C下活跃增殖。这些结果表明,本研究中提出的用于收获大量具有功能活性的猴子SSC的富集和体外培养方法可作为人类SSC有效体外扩增的基础。

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