Radial glial cells, present in many parts of the embryonic vertebrate
central nervous system (CNS), have been implicated in the guidance of
neuroblasts from the ventricular zone to their laminar destinations. M
oreover, radial glial cells may be progenitors of some CNS neurons and
glia. To gain new insight into the structure and development of these
cells, we have generated and characterized a panel of monoclonal anti
bodies that recognize radial glial cells of the chick optic tectum. Mi
ce were immunized with homogenates of embryonic day (E) 10 tectum, and
antibodies were analyzed by immunofluorescence and immunoblotting. We
describe here three pairs of antibodies. 1) H5 and a previously gener
ated antibody, R5 (Drager et al., J. Neurosci. 4:2025, 1984), stain th
e whole extent of the radial glial cell from E7 to E20. In cultures pr
epared from E10 tecta, both stain a filamentous meshwork in glial cell
s but not in neurons. On immunoblots, both recognize a protein of simi
lar to 52 kD that is closely related (or identical) to vimentin. 2) H2
8 and H29 stain radial glia between E7 and E14, but not later. Moreove
r, H28 and H29 staining is markedly more intense in the ventricular an
d intermediate zones than in the laminae of the tectal plate. Both of
these antibodies recognize an intracellular epitope in cultured glial
cells and a protein of similar to 35 kD on immunoblots. 3) H2 and H27
recognize antigens concentrated in the most superficial processes and
endfeet of radial glia in late (E16-E20) embryos. They stain distinct
structures in cultured glia, suggesting that they recognize distinct a
ntigens. H27 recognizes a protein of similar to 29 kD on immunoblots.
Thus antibodies H5 and R5 are good markers of radial glial cells at al
l stages, whereas the others define antigens that are developmentally
regulated and localized to discrete domains. Together, these antibodie
s can be used to study temporal and spatial specializations of radial
glia.