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Potier, B.

Publications and source records attributed to Potier, B..

2 recordsLinked to original sources

Principles of NMDA receptor co-agonism at cortical fast-spiking GABAergic interneurons in the adolescent prefrontal cortex

N-methyl-D-aspartate receptors (NMDARs) populate fast-spiking (FS)-parvalbumin-positive (PV+) GABAergic interneurons (INs), where they play a critical role in shaping circuit motifs and memory. However, it is largely unknown whether and how NMDARs at FS-PV+-INs are gated by their co-agonists and the functional relevance of such modulations for their synaptic coupling with excitatory neurons. Here, we report that FS-PV+-INs in the adolescent mouse prefrontal cortex, an area central to complex cognitive operation exhibit functional GluN2B/D containing NMDARs. These receptors contribute to the excitatory drive of FS-PV+-INs and to the feedforward inhibition, controlling short-term and long-term synaptic plasticity. While the identity of the co-agonist controlling GABAergic tone is tuned by the synaptic activity regime from D-serine to glycine, we reveal that it remains largely unchanged at the excitatory synapse with D-serine being the sole co-agonist gating NMDARs. Lastly, we show that D-serine-deficient mice, a model of NMDAR hypofunction show selective attenuation of PV+-INs excitation together with selective loss of temporal summation and long-term plasticity at the excitatory synapse. Our study reveals the segregation of pools of NMDARs at the soma and dendrites that are differently sensitive to D-serine or glycine, the existence of distinct modes of activity-dependent regulation of these NMDARs by their co-agonists at this major type of GABAergic INs, and hence the rules governing cortical inhibition by FS-PV+-INs during a critical period of late postnatal development.

neuroscience↗

BIN1 genetic risk factor for Alzheimer is sufficient to induce early structural tract alterations in entorhinal cortex-dentate gyrus pathway and related hippocampal multi-scale impairments

Genetic factors are known to contribute to Late Onset Alzheimers disease (LOAD) but their contribution to pathophysiology, specially to prodomic phases accessible to therapeutic approaches are far to be understood. To translate genetic risk of Alzheimers disease (AD) into mechanistic insight, we generated transgenic mouse lines that express a [~]195 kbp human BAC that includes only BIN1, a gene associated to LOAD. This model gives a modest BIN1 overexpression, dependent of the number of BAC copies. At 6 months of age, we detected impaired entorhinal cortex (EC)-hippocampal pathways with specific impairments in EC-dentate gyrus synaptic long-term potentiation, dendritic spines of granular cells and recognition episodic memory. Structural changes were quantified using MRI. Their whole-brain functional impact were analyzed using resting state fMRI with a hypoconnectivity centered on entorhinal cortex. These early phenotype defects independent of any changes in A-beta can be instrumental in the search for new AD drug targets.

neuroscience↗