Single-cell analysis of the developing human testis reveals somatic niche cell specification and fetal germline stem cell establishment

被引:155
作者
Guo, Jingtao [1 ,2 ,3 ]
Sosa, Enrique [4 ]
Chitiashvili, Tsotne [4 ,5 ]
Nie, Xichen [1 ,2 ]
Rojas, Ernesto Javier [4 ]
Oliver, Elizabeth [6 ,7 ]
Plath, Kathrin [5 ]
Hotaling, James M. [3 ]
Stukenborg, Jan-Bernd [6 ,7 ]
Clark, Amander T. [4 ]
Cairns, Bradley R. [1 ,2 ]
机构
[1] Univ Utah, Howard Hughes Med Inst, Dept Oncol Sci, Sch Med, Salt Lake City, UT 84112 USA
[2] Univ Utah, Sch Med, Huntsman Canc Inst, Salt Lake City, UT 84112 USA
[3] Univ Utah, Dept Surg, Div Urol, Sch Med, Salt Lake City, UT 84112 USA
[4] Univ Calif Los Angeles, Dept Mol Cell & Dev Biol, Los Angeles, CA 90095 USA
[5] Univ Calif Los Angeles, Dept Biol Chem, Los Angeles, CA 90095 USA
[6] Karolinska Inst, Dept Womens & Childrens Hlth, NORDFERTIL Res Lab Stockholm, Childhood Canc Res Unit,Bioclinicum J9 30, S-17164 Solna, Sweden
[7] Karolinska Univ Hosp, S-17164 Solna, Sweden
[8] DonorConnect, Murray, UT 84107 USA
基金
瑞典研究理事会;
关键词
LEYDIG; TRANSCRIPTOME; FATE;
D O I
10.1016/j.stem.2020.12.004
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Human testis development in prenatal life involves complex changes in germline and somatic cell identity. To better understand, we profiled and analyzed similar to 32,500 single-cell transcriptomes of testicular cells from embryonic, fetal, and infant stages. Our data show that at 6-7 weeks postfertilization, as the testicular cords are established, the Sertoli and interstitial cells originate from a common heterogeneous progenitor pool, which then resolves into fetal Sertoli cells (expressing tube-forming genes) or interstitial cells (including Leydig-lineage cells expressing steroidogenesis genes). Almost 10 weeks later, beginning at 14-16 weeks postfertilization, the male primordial germ cells exit mitosis, downregulate pluripotent transcription factors, and transition into cells that strongly resemble the state 0 spermatogonia originally defined in the infant and adult testes. Therefore, we called these fetal spermatogonia "state f0.'' Overall, we reveal multiple insights into the coordinated and temporal development of the embryonic, fetal, and postnatal male germline together with the somatic niche.
引用
收藏
页码:764 / +
页数:19
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