The present study has used two different approaches for labelling progenito
r cells at the optic vesicle stage in order to examine patterns of clonal e
xpansion and cellular dispersion within the developing retina. X-inactivati
on transgenic mice and chimeric mice expressing the lacZ reporter transgene
were examined during development and in adulthood to study the radial and
tangential dispersion of proliferating neuroepithelial cells and postmitoti
c retinal cells of known identities. Chimeric retinas were used to measure
tangential dispersion distances, while transgenic retinas were used to asse
ss the frequency of tangential dispersion for individual populations of ret
inal neurons. Tangential dispersion is shown to be a universal feature of p
articular retinal cell types, being contrasted with the strictly radial dis
persion of other cells. Tangential dispersion is a relatively short-distanc
e phenomenon, with distinct dispersion distances characteristic for cone, h
orizontal, amacrine and ganglion cells. Embryonic and postnatal retinas sho
w that tangential dispersion occurs at different times for these distinct c
ell types, associated with their times of differentiation rather than their
neurogenetic periods. These developmental results rule out the possibility
that tangential dispersion is due to a passive displacement produced by th
e proliferation of later-born cells, or to the lateral dispersion of a divi
ding sibling; rather, they are consistent with the hypothesis that tangenti
al dispersion plays a role in the establishment of the orderly spatial dist
ribution of retinal mosaics.