K. Uryu et al., Synaptogenesis and ultrastructural localization of the polysialylated neural cell adhesion molecule in the developing striatum, J COMP NEUR, 405(2), 1999, pp. 216-232
The polysialylated neural cell adhesion molecule (PSA-NCAM) plays a role in
axonal development and synaptic plasticity. Its pattern of expression is r
egulated temporally and topographically in the brain during development. Ho
wever, it is unclear whether or not its subcellular location also changes.
We have examined PSA-NCAM expression in relation to synapse formation in th
e developing rat striatum with immunohistochemistry and electron microscopy
. Early in development, PSA-NCAM was present along the cytoplasmic membrane
s of neurons and in growth cones. PSA-NCAM expression became progressively
confined to pre- and postsynaptic elements as neurons matured morphological
ly. Confirming previous results, a marked increase in the density of asymme
tric synapses determined by using the physical dissector method was observe
d in the dorsolateral striatum between postnatal day 14 (P14) and P18. It w
as followed by a reduction between P18 and P25, when asymmetric synapse den
sity reached adult levels. In contrast, the density of symmetric synapses h
ad surpassed adult levels by P14. In the dorsomedial striatum, the density
of asymmetric and symmetric synapses was similar at P18, at P25, and in adu
lts. PSA-NCAM was associated with most asymmetric and symmetric synapses at
P14 and P18 and was expressed in both pre- and postsynaptic elements of a
majority (P14) or approximately half(P18) of the synapses. Most synapses lo
st PSA-NCAM expression between P18 and P25 in the dorsolateral striatum and
between P25 and adult in the dorsomedial striatum. The data indicate that
PSA-NCAM expression becomes restricted topographically during neuronal matu
ration but remains strategically associated with developing synapses during
late postnatal development in the striatum. J. Comp. Neurol. 405:216-232,
1999. (C) 1999 Wiley-Liss, Inc.