Human primordial germ cell-like cells specified from resetting precursors develop in human hindgut organoids

被引:0
作者
Alves-Lopes, Joao Pedro [1 ,2 ,3 ,4 ]
Wong, Frederick C. K. [1 ,2 ,5 ]
Surani, M. Azim [1 ,2 ]
机构
[1] Univ Cambridge, Wellcome Canc Res UK Gurdon Inst, Cambridge, England
[2] Univ Cambridge, Dept Physiol Dev & Neurosci, Cambridge, England
[3] Karolinska Inst, NORDFERTIL Res Lab Stockholm, Dept Womens & Childrens Hlth, Childhood Canc Res Unit, J9 30, Stockholm, Sweden
[4] Karolinska Univ Hosp, Stockholm, Sweden
[5] Wellcome Trust Sanger Inst, Wellcome Genome Campus, Cambridge, England
基金
英国生物技术与生命科学研究理事会; 瑞典研究理事会; 英国惠康基金;
关键词
SPECIFICATION;
D O I
10.1038/s41596-023-00945-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Human primordial germ cells (hPGCs), the precursors of eggs and sperm, start their complex development shortly after specification and during their migration to the primitive gonads. Here, we describe protocols for specifying hPGC-like cells (hPGCLCs) from resetting precursors and progressing them with the support of human hindgut organoids. Resetting hPGCLCs (rhPGCLCs) are specified from human embryonic stem cells (hESCs) transitioning from the primed into the naive state of pluripotency. Hindgut organoids are also derived from hESCs after a sequential differentiation into a posterior endoderm/hindgut fate. Both rhPGCLCs and hindgut organoids are combined and co-cultured for 25 d. The entire procedure takes similar to 1.5 months and can be successfully implemented by a doctoral or graduate student with basic skills and experience in hESC cultures. The co-culture system supports the progression of rhPGCLCs at a developmental timing analogous to that observed in vivo. Compared with previously developed hPGCLC progression protocols, which depend on co-cultures with mouse embryonic gonadal tissue, our co-culture system represents a developmentally relevant model closer to the environment that hPGCs first encounter after specification. Together with the potential for investigations of events during hPGC specification and early development, these protocols provide a practical approach to designing efficient models for in vitro gametogenesis. Notably, the rhPGCLC-hindgut co-culture system can also be adapted to study failings in hPGC migration, which are associated with the etiology of some forms of infertility and germ cell tumors.
引用
收藏
页码:1149 / 1182
页数:40
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