A. Ikemoto et al., SYNAPTOPHYSIN EXPRESSION IN THE ANTERIOR HORN OF WERDNIG-HOFFMANN DISEASE, Journal of the neurological sciences, 136(1-2), 1996, pp. 94-100
This report concerns the study of synaptophysin (SP) expression in the
anterior horn in four cases of Werdnig-Hoffmann disease (WHD). All pa
tients had distinct anterior hom cell degeneration, and died before th
e age of one year. Normal spinal cords from five age-matched children
served as controls. Five cases of sporadic amyotrophic lateral scleros
is (S-ALS), three cases of lower motor neuron disease (L-MND), three c
ases of peripheral neuropathy with axonal reaction, and six adult case
s with normal spinal cords were included for comparison. Immunohistoch
emical techniques were used throughout. The results show that normal s
pinal cords of children have similar SP immunoreactivity patterns as t
hose of normal adults. We also found that despite relatively preserved
or slightly increased SP immunoreactivity on the surface of the cell
body and proximal processes of the remaining neurons, there was a diff
use decrease of immunoreaction product deposits in the anterior horn n
europil of the WHD cases. The ballooned neurons in the anterior horns
of patients with WHD, S-ALS, L-MND, and axonal reaction had few SP imm
unoreactive dots or granules around the cell bodies and proximal proce
sses. The perikarya of some ballooned neurons of the children with WHD
was diffusely stained for SP. There was no SP immunoreactive structur
es within the empty cell beds of these patients. The observed decrease
in SP expression around ballooned neurons in these disorders is indic
ative of a disconnection of presynaptic terminals of afferent fibers f
rom the proximal portion of the swollen degenerated anterior horn cell
s.