To investigate the role of neurotrophins in the initial formation of striat
al patch versus matrix, the spatial and temporal expression of trkB recepto
rs was examined using immunohistochemistry. Polyclonal antibodies, against
the C-terminus or the tyrosine kinase domain, revealed trkB-immunoreactive
cells and fibers localized to patches beginning on embryonic day 19 in the
rat, which co-localized with patchy dopamine fibers, substance P-immunoreac
tive neurons and glutamate receptors. Patchy striatal trkB expression was m
aintained after lesioning the nigrostriatal dopamine system. The patchy trk
B distribution persisted through postnatal day 14, then became more homogen
eous at the same time that nigrostriatal afferents become homogeneous. Late
r in development, trkB immunoreactivity was most intense in a subpopulation
of large striatal cells that were similar in size and frequency to those i
mmunoreactive for choline acetyltransferase.
The spatiotemporal expression of trkB receptor in phenotypically distinct s
triatal patches, as well as evidence that neurotrophins regulate expression
of neuronal phenotypic markers during development, may indicate a converge
nce of neurotrophins and afferent innervation on to future patch cells that
may regulate the establishment of striatal compartmentalization. (C) 1998
IBRO. Published by Elsevier Science Ltd.