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Enrichment of spermatogonial stem cells from long-term cultured human testicular cells

机译:长期培养的人睾丸细胞对精原干细胞的富集

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Objective To evaluate the degree of enrichment of spermatogonial stem cells (SSCs) from human testicular cell cultures by ITGA6+, HLA -/ITGA6+, GPR125+, and HLA-/ GPR125+ magnetic-assisted cell sorting (MACS). Design Experimental basic science study. Setting Reproductive biology laboratory. Patient(s) Multiple samples of cryopreserved human testicular cells from two prostate cancer patients with normal spermatogenesis. Intervention(s) Cultured human testicular cells subjected to four sorting strategies based on MACS and xenotransplanted to the testes of mice to determine the enrichment for SSCs. Main Outcome Measure(s) Enrichment for human spermatogonia and SSCs tested by expression analysis of spermatogonial markers ITGA6, GPR125, ZBTB16, UCHL1, and ID4 using quantitative real-time polymerase chain reaction (qPCR) and by xenotransplantation into the testes of mice, respectively. Result(s) Compared with the nonsorted cultured testicular cells, only the ITGA6+ and HLA-/GPR125+ sorted cells showed enrichment for ID4. No difference in expression of ZBTB16 and UCHL1 was observed. Xenotransplantation of the sorted cell fractions showed a 7.1-fold enrichment of SSCs with ITGA6+. Conclusion(s) Magnetic-assisted cell sorting of cultured human testicular cells using ITGA6 allows for enrichment of SSCs, which aids in further molecular characterization of cultured human SSCs and enhances testicular colonization upon transplantation in future clinical settings.
机译:目的评估ITGA6 +,HLA- / ITGA6 +,GPR125 +和HLA- / GPR125 +磁辅助细胞分选(MACS)对人睾丸细胞培养物中精原干细胞(SSCs)的富集程度。设计实验基础科学研究。设置生殖生物学实验室。患者两名精子正常的前列腺癌患者的冷冻保存的人类睾丸细胞的多个样本。干预对培养的人类睾丸细胞进行了基于MACS的四种分选策略,并将其异种移植到小鼠的睾丸中以确定SSC的富集。通过使用定量实时聚合酶链反应(qPCR)对精原标志物ITGA6,GPR125,ZBTB16,UCHL1和ID4的表达分析,以及通过异种移植到小鼠睾丸中,分别测试了人类精原细胞和SSC的主要富集指标。结果与未分选的睾丸细胞相比,仅ITGA6 +和HLA- / GPR125 +分选的细胞对ID4富集。没有观察到ZBTB16和UCHL1的表达差异。分选的细胞级分的异种移植显示ITGA6 +富集SSC的7.1倍。结论使用ITGA6对培养的人睾丸细胞进行磁辅助细胞分选有助于SSC的富集,这有助于进一步培养培养的人SSC的分子,并在将来的临床环境中移植时增强睾丸的定殖。

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