4.7 Article

Activation of Extrasynaptic Kainate Receptors Drives Hilar Mossy Cell Activity

期刊

JOURNAL OF NEUROSCIENCE
卷 42, 期 14, 页码 2872-2884

出版社

SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.0922-21.2022

关键词

CA3; dentate gyrus; epilepsy; GluK2; kainic acid; mossy fiber

资金

  1. National Institutes of Health [R01-NS-113600, R01-MH-116673, R01-MH-125772]
  2. Japan Society for the Promotion of Science (JSPS) [20H05628, 21H02589]
  3. JSPS KAKENHI [17H0631310, 20H03410]
  4. Grants-in-Aid for Scientific Research [21H02589, 20H03410, 20H05628] Funding Source: KAKEN

向作者/读者索取更多资源

This study provides the first direct evidence of functional extrasynaptic kainate receptors (KARs) on mossy cells (MCs) in the hippocampus. These KARs are mainly located extrasynaptically and play a critical role in the activity of MCs. Increases in ambient glutamate can activate the KARs on MCs.
Mossy cells (MCs) of the dentate gyrus are key components of an excitatory associative circuit established by reciprocal connections with dentate granule cells (GCs). MCs are implicated in place field encoding, pattern separation, and novelty detection, as well as in brain disorders such as temporal lobe epilepsy and depression. Despite their functional relevance, little is known about the determinants that control MC activity. Here, we examined whether MCs express functional kainate receptors (KARs), a subtype of glutamate receptors involved in neuronal development, synaptic transmission, and epilepsy. Using mouse hippocampal slices, we found that bath application of submicromolar and micromolar concentrations of the KAR agonist kainic acid induced inward currents and robust MC firing. These effects were abolished in GluK2 KO mice, indicating the presence of functional GluK2-containing KARs in MCs. In contrast to CA3 pyramidal cells, which are structurally and functionally similar to MCs and express synaptic KARs at mossy fiber (MF) inputs (i.e., GC axons), we found no evidence for KAR-mediated transmission at MF-MC synapses, indicating that most KARs at MCs are extrasynaptic. Immunofluorescence and immunoelectron microscopy analyses confirmed the extrasynaptic localization of GluK2-containing KARs in MCs. Finally, blocking glutamate transporters, a manipulation that increases extracellular levels of endogenous glutamate, was sufficient to induce KAR-mediated inward currents in MCs, suggesting that MC-KARs can be activated by increases in ambient glutamate. Our findings provide the first direct evidence of functional extrasynaptic KARs at a critical excitatory neuron of the hippocampus.

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