Ij. Weiler et Wt. Greenough, METABOTROPIC GLUTAMATE RECEPTORS TRIGGER POSTSYNAPTIC PROTEIN-SYNTHESIS, Proceedings of the National Academy of Sciences of the United Statesof America, 90(15), 1993, pp. 7168-7171
K+ depolarization or addition of glutamate to a synaptoneurosome prepa
ration triggers a rapid increase in size of polyribosomal aggregates i
solated by centrifugation of lysate through 1 M sucrose. The profile o
f response to the glutamate analogues quisqualate, ibotenate, and 1-am
inocyclopentane-1,3-dicarboxylate corresponds to that of metabotropic
receptors. Glutamate stimulation is mimicked by the diacylglycerol ana
logue 1-oleoyl-2-acetylglycerol and by the protein kinase C activator
phorbol dibutyrate. The phospholipase blockers 2-nitro-4-carboxyphenyl
-N,N-diphenylcarbamate and quinacrine reduce the late phase of the res
ponse. The protein kinase C inhibitor calphostin C suppresses the resp
onse to 1-aminocyclopentane-1,3-dicarboxylate. These data indicate tha
t glutamatergic synapses upregulate postsynaptic protein synthesis via
metabotropic glutamate receptors coupled to the phosphatidylinositol
second-messenger system. This mechanism could underlie the reported in
volvement of metabotropic glutamate receptors in long-term potentiatio
n and other forms of neural plasticity.