Primordial germ cells (PGCs) are the founder cell population of the ga
metes which form during the sexually mature stage of the life cycle. I
n the mouse, they arise early in embryogenesis, first becoming visible
in the extraembryonic mesoderm, posterior to the primitive streak, at
7.5 days post coitum (d.p.c.). They subsequently become incorporated
into the epithelium of the hind gut, from which they emigrate (9.5 d.p
.c.) and move first into the dorsal mesentery (10.5 d.p.c.), and then
into the genital ridges that lie on the dorsal body wall (11.5 d.p.c.)
. We have used confocal microscopy to study PGCs stained with an antib
ody that reacts with a carbohydrate antigen (Stage-Specific Embryonic
Antigen-1, SSEA-1) carried on the PGC surface. This allows the study o
f the whole PGC surface, at different stages of their migration. The a
ppearance of PGCs in tissue sections has given rise to the conventiona
l view that they migrate as individuals, each arriving in turn at the
genital ridge. In this paper, we show that PGCs leave the hind gut ind
ependently, but then extend long (up to 40 mu m) processes, with which
they link up to each other to form extensive networks. During the 10.
5-11.5 d.p.c. period, these networks of PGCs aggregate into groups of
tightly apposed cells in the genital ridges. As this occurs, their pro
cesses are lost, and their appearance suggests they are now non-motile
. Furthermore, we find that PGCs taken from the dorsal mesentery at 10
.5 d.p.c. perform the same sequence of movements in culture. At first
they are actively locomotory. They become linked to other PGCs via lon
g processes and form clusters of nonmotile cells. This aggregation tog
ether into closely apposed masses may be an important component of PGC
migration from the gut into the genital ridges and would also allow s
ignalling interactions between PGCs. We show also that the first PGCs
to emigrate from the hind gut, between 9 and 9.5 d.p.c., do so directl
y into the area where the genital ridges will form. This suggests that
an adhesive interaction between these 'pioneer germ cells' and the ta
rget tissue may play a role in the localisation of PGCs into the genit
al ridges as they aggregate.