W. Li et al., C-TERMINALS ON MOTONEURONS - ELECTRON-MICROSCOPE LOCALIZATION OF CHOLINERGIC MARKERS IN ADULT-RATS AND ANTIBODY-INDUCED DEPLETION IN NEONATES, Neuroscience, 65(3), 1995, pp. 879-891
C-terminals on motoneurons are defined as those accompanied by charact
eristic postsynaptic specializations termed subsurface cisterns. We ha
ve previously shown, by light microscope immunolabelling methods, that
subsurface cisterns occur regularly beneath choline acetyltransferase
- and acetylcholinesterase-containing boutons on motoneurons. In the p
resent study, the cholinergic nature of C-terminals suggested by these
results was further investigated by immunohistochemistry and electron
microscopy in adult rats and in neonates treated with a murine monocl
onal acetylcholinesterase antibody which was previously shown to cause
immunological lesions of central cholinergic systems. In both the fac
ial nucleus and lumbar segment of spinal cord of adult rats, C-termina
ls were seen intensely immunostained for the cholinergic markers choli
ne acetyltransferase and acetylcholinesterase. Immunolabelled terminal
s made contact with either neuronal somata or large calibre dendrites,
which were positive for the cholinergic markers, and exhibited club-s
haped or thin elongated morphologies suggestive of terminal or ell pas
sant type synaptic interactions. The close relationship found between
cholinergic markers and immunolabelled subsurface cisterns in adults w
as maintained on motoneurons of eight-day-old rats. While subcutaneous
treatment of newborn rat with acetylcholinesterase antibody appeared
to have no effect on the distribution of immunopositive subsurface cis
terns in motoneurons when examined on postnatal day 8, the density of
labelling for the two cholinergic markers around these neurons was red
uced. Areas of neuropil immediately surrounding motoneurons in treated
animals often showed signs of extensive swelling and deterioration in
dicative of a lesion event, and these motoneurons frequently displayed
subsurface cisterns unapposed to C-terminals. These results support o
ur earlier conclusion, based on light microscope investigation, that t
he majority if not all C-terminals are cholinergic in the areas invest
igated and demonstrate the potential utility of immunolesion methods i
n the study of C-terminal function.