4.6 Article

Group I mGluR-Mediated Activation of Martinotti Cells Inhibits Local Cortical Circuitry in Human Cortex

Journal

FRONTIERS IN CELLULAR NEUROSCIENCE
Volume 13, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fncel.2019.00315

Keywords

mGluR; human cortex; Martinotti; fast-spiking interneuron; LTD; single-cell RNA-sequencing

Categories

Funding

  1. Netherlands Organization for Scientific Research (NWO
  2. VICI grant ) [016.140.610]
  3. ERC starting grant BrainSignals
  4. European Union's Horizon 2020 Framework Programme for Research and Innovation [785907]
  5. Netherlands Organization for Scientific Research (NWO VIDI grant) [917.10.372]
  6. Fondation Jerome LeJeune
  7. Hersenstichting NL [2013(1)-229]

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Group I metabotropic glutamate receptors (mGluRs) mediate a range of signaling and plasticity processes in the brain and are of growing importance as potential therapeutic targets in clinical trials for neuropsychiatric and neurodevelopmental disorders (NDDs). Fundamental knowledge regarding the functional effects of mGluRs upon pyramidal neurons and interneurons is derived largely from rodent brain, and their effects upon human neurons are predominantly untested. We therefore addressed how group I mGluRs affect microcircuits in human neocortex. We show that activation of group I mGluRs elicits action potential firing in Martinotti cells, which leads to increased synaptic inhibition onto neighboring neurons. Some other interneurons, including fast-spiking interneurons, are depolarized but do not fire action potentials in response to group I mGluR activation. Furthermore, we confirm the existence of group I mGluR-mediated depression of excitatory synapses in human pyramidal neurons. We propose that the strong increase in inhibition and depression of excitatory synapses onto layer 2/3 pyramidal neurons upon group I mGluR activation likely results in a shift in the balance between excitation and inhibition in the human cortical network.

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