生物
生殖系
细胞生物学
胚胎干细胞
生殖细胞
SMAD公司
信号转导
成纤维细胞生长因子
遗传学
基因
受体
作者
Jemima Whyte,James D. Glover,Mark Woodcock,Joanna Brzeszczyńska,Lorna Taylor,Adrian Sherman,Pete Kaiser,Michael J. McGrew
标识
DOI:10.1016/j.stemcr.2015.10.008
摘要
Precise self-renewal of the germ cell lineage is fundamental to fertility and reproductive success. The early precursors for the germ lineage, primordial germ cells (PGCs), survive and proliferate in several embryonic locations during their migration to the embryonic gonad. By elucidating the active signaling pathways in migratory PGCs in vivo, we were able to create culture conditions that recapitulate this embryonic germ cell environment. In defined medium conditions without feeder cells, the growth factors FGF2, insulin, and Activin A, signaling through their cognate-signaling pathways, were sufficient for self-renewal of germline-competent PGCs. Forced expression of constitutively active MEK1, AKT, and SMAD3 proteins could replace their respective upstream growth factors. Unexpectedly, we found that BMP4 could replace Activin A in non-clonal growth conditions. These defined medium conditions identify the key molecular pathways required for PGC self-renewal and will facilitate efforts in biobanking of chicken genetic resources and genome editing.
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