Premium
Bidirectional modulation of glutamatergic synaptic transmission by metabotropic glutamate type 7 receptors at Schaffer collateral–CA1 hippocampal synapses
Author(s) -
Martín Ricardo,
Ferrero José Javier,
ColladoAlsina Andrea,
Aguado Carolina,
Luján Rafael,
Torres Magdalena,
SánchezPrieto José
Publication year - 2018
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jp275371
Subject(s) - metabotropic glutamate receptor , long term depression , neurotransmission , metabotropic receptor , metabotropic glutamate receptor 7 , metabotropic glutamate receptor 1 , metabotropic glutamate receptor 6 , biology , glutamate receptor , chemistry , receptor , ampa receptor , biochemistry
Key points Neurotransmitter release is inhibited by metabotropic glutamate type 7 (mGlu 7 ) receptors that reduce Ca 2+ influx, yet synapses lacking this receptor also produce weaker release, suggesting that mGlu 7 receptors may also prime synaptic vesicles for release. Prolonged activation of mGlu 7 receptors with the agonist l ‐AP4 first reduces and then enhances the amplitude of EPSCs through a presynaptic effect. The inhibitory response is blocked by pertussis toxin, while the potentiating response is prevented by a phospholipase C inhibitor (U73122) and an inhibitor of diacylglycerol (DAG) binding (calphostin C), suggesting that this receptor also couples to pathways that generate DAG. Release potentiation is associated with an increase in the number of synaptic vesicles close to the plasma membrane, which was dependent on the Munc13‐2 and RIM1α proteins. The Glu7 receptors activated by the glutamate released following high frequency stimulation provoke a bidirectional modulation of synaptic transmission.Abstract Neurotransmitter release is driven by Ca 2+ influx at synaptic boutons that acts on synaptic vesicles ready to undergo exocytosis. Neurotransmitter release is inhibited when metabotropic glutamate type 7 (mGlu 7 ) receptors provoke a reduction in Ca 2+ influx, although the reduced release from synapses lacking this receptor suggests that they may also prime synaptic vesicles for release. These mGlu 7 receptors activate phospholipase C (PLC) and generate inositol trisphosphate, which in turn releases Ca 2+ from intracellular stores and produces diacylglycerol (DAG), an activator of proteins containing DAG‐binding domains such as Munc13 and protein kinase C (PKC). However, the full effects of mGlu 7 receptor signalling on synaptic transmission are unclear. We found that prolonged activation of mGlu 7 receptors with the agonist l ‐AP4 first reduces and then enhances the amplitude of EPSCs, a presynaptic effect that changes the frequency but not the amplitude of the mEPSCs and the paired pulse ratio. Pertussis toxin blocks the inhibitory response, while the PLC inhibitor U73122, and the inhibitor of DAG binding calphostin C, prevent receptor mediated potentiation. Moreover, this DAG‐dependent potentiation of the release machinery brings more synaptic vesicles closer to the active zone plasma membrane in a Munc13‐2‐ and RIM1α‐dependent manner. Electrically evoked release of glutamate that activates mGlu 7 receptors also bidirectionally modulates synaptic transmission. In these conditions, potentiation now occurs rapidly and it overcomes any inhibition, such that potentiation prevails unless it is suppressed with the PLC inhibitor U73122.