Journal of Neuroscience, Vol 9, 3753-3759, Copyright © 1989 by Society for Neuroscience
Muscarinic receptor activation stimulates B-50/GAP43 phosphorylation in isolated nerve growth cones
CO Van Hooff, PN De Graan, AB Oestreicher and WH Gispen
Division of Molecular Neurobiology, Rudolf Magnus Institute, University of Utrecht, The Netherlands.
A characteristic feature of neurite formation is high expression of the
phosphoprotein B-50/GAP43. Previous studies with growth cone membranes have
indicated that this neuron-specific protein kinase C substrate may be
involved in transmembrane signal transduction at the growth cone. We
monitored the degree of phosphorylation of B-50 by quantitative B-50
immunoprecipitation from intact nerve growth cones, isolated from 5-day-
old rat brain and prelabeled with 32P-orthophosphate. B-50 phosphorylation
in nerve growth cones is stimulated by 4 beta-phorbol 12,13-dibutyrate
(PDB) and 1,2-dioctanoylglycerol (DOG) in a concentration-dependent manner,
but not by 4 alpha-phorbol 12,13- didecanoate (4 alpha-PDD). These results
confirm that B-50 is a substrate of PKC in intact growth cones.
Depolarization induced by 30 mM K+ produces a transient increase in B-50
phosphorylation, which is maximal after 15 sec and declines to basal level
within 5 min. This rise in B-50 phosphorylation can be partially blocked by
atropine (10(- 3)-10(-4) M), suggesting the involvement of muscarinic
receptors. Indeed, the cholinergic receptor agonist carbachol enhances B-50
phosphorylation in a concentration-dependent manner (50% at 10(-3) M).
Since the effect of carbachol (10(-3) M) can be blocked by atropine (10(-7)
M), we conclude that this increase in B-50 phosphorylation is mediated
through activation of the muscarinic receptors on the growth cones. The
carbachol-induced stimulation is further increased by concurrent
K+-depolarization. The effects of carbachol and depolarization are
additive. To our knowledge, this is the first report showing
receptor-mediated effects on the PKC substrate B-50 in growth cones. Our
data support the hypothesis that phosphorylation of B-50 by PKC is involved
in signal transduction in nerve growth cones.