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从长期培养的人睾丸细胞中富集精原干细胞。

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

作者信息

Nickkholgh Bita, Mizrak Sefika Canan, Korver Cindy M, van Daalen Saskia K M, Meissner Andreas, Repping Sjoerd, van Pelt Ans M M

机构信息

Center for Reproductive Medicine, Women's and Children's Hospital, Academic Medical Center, University of Amsterdam, Amsterdam, the Netherlands.

Center for Reproductive Medicine, Women's and Children's Hospital, Academic Medical Center, University of Amsterdam, Amsterdam, the Netherlands.

出版信息

Fertil Steril. 2014 Aug;102(2):558-565.e5. doi: 10.1016/j.fertnstert.2014.04.022. Epub 2014 May 23.

Abstract

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.

摘要

目的

通过整合素α6(ITGA6)阳性、人白细胞抗原阴性/整合素α6阳性(HLA-/ITGA6+)、G蛋白偶联受体125(GPR125)阳性以及人白细胞抗原阴性/G蛋白偶联受体125阳性的磁性辅助细胞分选(MACS),评估从人睾丸细胞培养物中富集精原干细胞(SSCs)的程度。

设计

实验基础科学研究。

地点

生殖生物学实验室。

患者

来自两名精子发生正常的前列腺癌患者的多份冷冻保存的人睾丸细胞样本。

干预措施

将培养的人睾丸细胞基于MACS进行四种分选策略处理,并异种移植到小鼠睾丸中以确定SSCs的富集情况。

主要观察指标

分别通过定量实时聚合酶链反应(qPCR)对精原细胞标志物ITGA6、GPR125、锌指蛋白16(ZBTB16)、泛素羧基末端水解酶L1(UCHL1)和ID4进行表达分析,以及通过异种移植到小鼠睾丸中,来检测人精原细胞和SSCs的富集情况。

结果

与未分选的培养睾丸细胞相比,只有ITGA6+和HLA-/GPR125+分选的细胞显示出ID4的富集。未观察到ZBTB16和UCHL1表达的差异。分选细胞组分的异种移植显示ITGA6+的SSCs富集了7.1倍。

结论

使用ITGA6对培养的人睾丸细胞进行磁性辅助细胞分选可实现SSCs的富集,这有助于对培养的人SSCs进行进一步的分子表征,并在未来临床环境中移植时增强睾丸定植。

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