The germ cell lineage in the mouse is not predetermined but is established
during gastrulation, in response to signalling molecules acting on a subset
of epiblast cells that move through the primitive streak together with ext
ra-embryonic mesoderm precursors. After migration to the site of the future
gonads, germ cell sex determination is achieved, with germ cell phenotype
in male and female embryos diverging. Evidence suggests that all germ cells
spontaneously take the female pathway, entering prophase of the first meio
tic division five or six days after the birth of the germ cell lineage, wit
h the exception of those located in the embryonic testis, which exit the ce
ll cycle in response to some inhibitory signal and remain in G(o) until aft
er birth, when spermatogenesis begins. In culture, germ cells respond to ce
rtain growth factors by proliferating indefinitely. These immortalized embr
yonic germ (EG) cell lines are chromosomally stable and pluripotent, closel
y resembling the embryonic stem (ES) cell lines derived from blastocyst-sta
ge embryos. Human EG and ES cell lines have recently been made, raising the
hope that their differentiation could be directed to specific cell types,
of value in the clinical treatment of degenerative diseases.