Journal of Neuroscience, Vol 16, 148-158, Copyright © 1996 by Society for Neuroscience
Localization of L-type Ca2+ channels at perisynaptic glial cells of the frog neuromuscular junction
R Robitaille, MJ Bourque and S Vandaele
Departement de Physiologie, Universite de Montreal, Canada.
The presence of L-type Ca2+ channels at the frog neuromuscular junction
(nmj) was studied by monitoring changes in intracellular Ca2+ evoked in
presynaptic terminals and perisynaptic Schwann cells (PSCs) and by studying
the distribution of Ca2+ channels using a monoclonal antibody directed
against the alpha 2/delta subunit of L channels. L-type Ca2+ channel
agonist and antagonist had no effect on resting level of fluorescence and
nerve-evoked Ca2+ responses in presynaptic terminals. However,
depolarization of PSCs induced by KCl (25 mM) produced entry of Ca2+, which
was prevented by L-type Ca2+ channel blockers, in (+)R Bay K 8644 of
nimodipine. Labeling of Ca2+ channels revealed an intracellular epitope
with an irregular and spotty distribution along the endplate. Similar
results were obtained with a fluorescent phenylalkylamine
[(-)DM-BODIPY-PAA], a blocker of L-type Ca2+ channels. Ca2+ channel
labeling remained in absence of nerve terminals but was absent after
mechanical removal of nerve terminals and PSCs. Most Ca2+ channel spots
were distributed in between bands of cholinergic receptors labeled with
alpha-bungarotoxin-TRITC. Cross sections of motor endplates revealed that
labeling of Ca2+ channels was found only at the level of the synaptic cleft
and not all around the PSCs. We conclude that L-type Ca2+ channels are
located in perisynaptic glial cells in an appropriate location to sense
depolarization induced by neurotransmitters and thus may support possible
roles of glial cells on synaptic function.