关键词: Esrrb Nanog Otx2 embryonic stem cells epiblast-like cells germline primordial germ cells

Mesh : Biomarkers Cell Differentiation / genetics Cells, Cultured Gene Expression Regulation, Developmental Gene Knockdown Techniques Genetic Heterogeneity Germ Cells / cytology metabolism Immunophenotyping Nanog Homeobox Protein / genetics metabolism Otx Transcription Factors / genetics metabolism Protein Binding Receptors, Estrogen / genetics metabolism

来  源:   DOI:10.1016/j.stemcr.2021.11.013

Abstract:
Primordial germ cells (PGCs) arise from cells of the post-implantation epiblast in response to cytokine signaling. PGC development can be recapitulated in vitro by differentiating epiblast-like cells (EpiLCs) into PGC-like cells (PGCLCs) through cytokine exposure. Interestingly, the cytokine requirement for PGCLC induction can be bypassed by enforced expression of the transcription factor (TF) NANOG. However, the underlying mechanisms are not fully elucidated. Here, we show that NANOG mediates Otx2 downregulation in the absence of cytokines and that this is essential for PGCLC induction by NANOG. Moreover, the direct NANOG target gene Esrrb, which can substitute for several NANOG functions, does not downregulate Otx2 when overexpressed in EpiLCs and cannot promote PGCLC specification. However, expression of ESRRB in Otx2+/- EpiLCs rescues emergence of PGCLCs. This study illuminates the interplay of TFs occurring at the earliest stages of PGC specification.
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