Establishment of the Long‐Term In Vitro Culture System for Chicken Primordial Germ Cells

Contents The objective of this study was to establish the long‐term in vitro culture system for chicken gonadal primordial germ cells (gPGCs). Primitive gonads collected from 5.5‐day‐old chicken embryos were dissociated and explanted onto plates pre‐coated with 0.1% gelatin. Each of the four different conditioned media from proliferating and mitotically inactivated chicken embryonic fibroblast (CEF) cells and murine embryonic fibroblasts (STO cells, CRL‐1053, ATCC, USA), respectively, was supplemented with growth factors and used to support the growth of gPGCs. The result showed that all the conditioned media could promote the growth and colony formation of gPGCs in vitro , in particular the medium conditioned by inactivated CEF cells. The gPGC‐derived colonies maintained in inactivated CEF cells‐conditioned medium up to 281 days were positively stained by periodic acid Schiff reaction and antibodies specific to anti‐SSEA‐1, SSEA‐3, SSEA‐4, integrin α6 and integrin β1. Their capacities of migration via vascular system and taking up residence in the primary gonadal ridge were further demonstrated by transferring to the dorsal aorta of stage 17 recipient embryos. These results suggested that our culture system is able to maintain chicken gPGCs for long‐term in vitro culture without losing their capacity to express pluripotent markers and to integrate into the gonads.