Group I Metabotropic Glutamate Receptor Signaling via G alpha q/G alpha 11 Secures the Induction of Long-Term Potentiation in the Hippocampal Area CA1

• Published in: The Journal of neuroscience Vol. 22; no. 19; pp. 8379 - 8390
• Main Authors: Miura, Masami, Watanabe, Masahiko, Offermanns, S, Simon, MI, Kano, Masanobu
• Format: Journal Article
• Language: English
• Published: 01.10.2002
• ISSN: 0270-6474

Heterotromeric G-proteins of the Gq family are thought to transduce signals from group I metabotropic glutamate receptors (mGluRs) in central neurons. We investigated roles of this cascade in hippocampal long-term potentiation (LTP) by using null-mutant mice lacking the alpha subunit of Gq (G alpha q) or G11 (G alpha 11). We found no obvious abnormalities in the morphology, layer structure, expression of NMDA receptors, and basic parameters of excitatory synaptic transmission in the hippocampus of G alpha q mutant mice. We used theta burst stimulation (TBS) (3-10 burst trains at 5 Hz; each train consisted of five stimuli at 100 Hz) to induce LTP at Schaffer collateral to CA1 pyramidal cell synapses. Conventional TBS with 10 burst trains induced robust LTP in wild-type, G alpha q mutant, and G alpha 11 mutant mice. Weak TBS with three burst trains consistently induced LTP in wild-type mice. In contrast, the same weak TBS was insufficient to induce LTP in G alpha q and G alpha 11 mutant mice. In wild-type mice, the LTP by weak TBS was abolished by inhibiting group I mGluR or protein kinase C (PKC) but not by blocking muscarinic acetylcholine receptors. Prior activation of group I mGluR by an agonist significantly enhanced the LTP by weak TBS in wild-type mice. However, this priming effect was absent in G alpha q mutant mice. These results indicate that the signaling from group I mGluR to PKC involving G alpha q/G alpha 11 does not constitute the main pathway for LTP, but it secures LTP induction by lowering its threshold in the hippocampal area CA1.