The aim of this study was to produce monoclonal antibodies specific for neu
rones that are generated earliest in the rat neocortex. One of the establis
hed clones, K1. showed a strong immunoreactivity in the marginal zone at th
e 19th day of gestation (E19). The immunoreactivity of K1 initially appeare
d in the primordial plexiform layer at E15, in the subplate at E16, and in
the marginal zone by E17. It became undetectable in the first postnatal wee
k. The immunoreactivity was not detected in the neocortex of adults or elde
rly. Western blotting analysis revealed reactive bands at positions corresp
onding to proteins of 290 and 280 kDa for the neocortical membrane fraction
s prepared from E16 to E21 embryos In these stages, smears of bands were al
so found at positions corresponding to higher molecular weights. A single b
and of protein of 280 kDa was detected for the soluble fractions prepared f
rom the embryos at E19 and E21. These reactivities were susceptible to prot
ease, but not to enzymatic or chemical destruction of carbohydrate residues
. Electron microscopic analysis showed that the K1 immunoreactivity was det
ected primarily on the cellular membranes of neurites. In the marginal zone
at E19, the K1 immunoreactivity was localised where neurites make contact
with other neurites or somata. A portion of these contact points had typica
l features of synapses. In the cortical plate of the same stage, arrays of
tiny K1-immunoreactive puncta were observed on a subset of radial processes
. These results suggest that monoclonal antibody K1 is a marker recognising
neurites of subplate neurones that extend radially and make neuronal conta
cts in the marginal zone.(C) 2001 Elsevier Science Ireland Ltd and the Japa
n Neuroscience Society. All rights reserved.