Reconstitution of human fetal ovaries reveals niche requirements for primordial germ cell-like cell progression
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Human primordial germ cell-like cells (hPGCLCs) can be specified from human induced pluripotent stem cells (hiPSCs), offering a valuable model for human germ cell development. However, further maturation steps of hPGCLCs rely on mouse feeders, or co-culture with mouse gonadal somatic cells. Exposure of hPGCLCs to human embryonic niche has not been attempted. Here, we co-cultured female hPGCLCs in two distinct somatic compartments. In reconstituted ovary (rOv) culture, human fetal germ cells proliferate and initiate meiosis, while hPGCLCs upregulate gonadal germ cell markers such as DDX4. Additionally, hPGCLCs can be supported in 3D culture by the amnion-like cells (AMLC) generated during PGCLC differentiation. Compared to rOV, hPGCLCs are less prone to dedifferentiation in PGCLC/AMLC aggregates. Finally, we demonstrated that SCF is crucial for the survival of hPGCLCs but not second trimester fetal germ cells. Together, this work highlights a shift in niche is required in human germ cell development.
In Brief
Chang and colleagues utilized in vitro reconstituted human fetal ovary (rOv) as somatic niche to mature human primordial germ cell-like cells (PGCLCs). hPGCLCs in rOv upregulate gonadal germ cell markers but are prone to dedifferentiation. In contrast, hPGCLCs cultured with amnion-like cells can be maintained without dedifferentiation. In both culture systems, SCF is crucial for the survival of hPGCLCs.
Highlights
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Reconstituted human fetal ovaries (rOvs) support meiosis entry of fetal germ cells
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The rOVs support hPGCLCs to upregulate gonadal germ cell markers
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hPGCLCs show less dedifferentiation in amnion-like cell aggregates compare to rOv
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SCF is not required for survival of fetal germ cells, but crucial for hPGCLCs
