Segregation of Kainate and AMPA Synapses
نویسندگان
چکیده
Kainate receptors have long been the poor stepchildren of the ionotropic glutamate receptor family. First, they were named for an agonist that also activates AMPA receptors. Then, even after molecular cloning established their unique composition, their small conductance and the lack of selective antagonists hampered study. However, their presynaptic and postsynaptic function is now well established in several brain regions, including layer IV of the barrel cortex. There, glutamatergic transmission abruptly switches from kainateto AMPA receptor-mediated transmission during the first postnatal week. This week, Bannister et al. report that this developmental switch is associated with total segregation of these receptors, indicating that individual synapses use either kainate or AMPA receptors, but not both. The authors used strontium to evoke single quantal events. Kainate receptor-mediated events had small quantal amplitude, slow kinetics, and large charge transfer, whereas AMPA-mediated transmission had larger quanta, fast kinetics, and small charge transfer. The slow kainate receptor kinetics could not be attributed to an extrasynaptic localization.
منابع مشابه
Developmental changes in AMPA and kainate receptor-mediated quantal transmission at thalamocortical synapses in the barrel cortex.
During the first week of life, there is a shift from kainate to AMPA receptor-mediated thalamocortical transmission in layer IV barrel cortex. However, the mechanisms underlying this change and the differential properties of AMPA and kainate receptor-mediated transmission remain essentially unexplored. To investigate this, we studied the quantal properties of AMPA and kainate receptor-mediated ...
متن کاملQuantal Release of Glutamate Generates Pure Kainate and Mixed AMPA/Kainate EPSCs in Hippocampal Neurons
The relative contribution of kainate receptors to ongoing glutamatergic activity is at present unknown. We report the presence of spontaneous, miniature, and minimal stimulation-evoked excitatory postsynaptic currents (EPSCs) that are mediated solely by kainate receptors (EPSC(kainate)) or by both AMPA and kainate receptors (EPSC(AMPA/kainate)). EPSC(kainate) and EPSC(AMPA/kainate) are selectiv...
متن کاملAttenuated plasticity of postsynaptic kainate receptors in hippocampal CA3 pyramidal neurons.
Kainate receptor-mediated components of postsynaptic currents at hippocampal mossy fiber synapses have markedly slower kinetics than currents arising from AMPA receptors. Here, we demonstrate that other aspects of kainate and AMPA receptor function at this synapse are distinct; in particular, kainate receptor currents are less sensitive to short- and long-term increases in presynaptic strength....
متن کاملStargazin differentially controls the trafficking of alpha-amino-3-hydroxyl-5-methyl-4-isoxazolepropionate and kainate receptors.
Synaptic plasticity at excitatory synapses in the brain is largely achieved by rapid changes in the number of synaptic alpha-amino-3-hydroxyl-5-methyl-4-isoxazolepropionate (AMPA) receptors. Stargazin, a membrane protein that interacts with AMPA receptors, is believed to play a pivotal role in trafficking AMPA receptors to the plasma membrane and targeting them to the synapse. However, it is un...
متن کاملKainate receptors depress excitatory synaptic transmission at CA3-->CA1 synapses in the hippocampus via a direct presynaptic action.
Kainate receptor activation depresses synaptic release of neurotransmitter at a number of synapses in the CNS. The mechanism underlying this depression is controversial, and both ionotropic and metabotropic mechanisms have been suggested. We report here that the AMPA/kainate receptor agonists domoate (DA) and kainate (KA) cause a presynaptic depression of glutamatergic transmission at CA3-->CA1...
متن کامل