Embryonic cortical layer 5 pyramidal neurons form an active, transient circuit motif perturbed by autism-associated mutations
Martin MunziD, Arjun BhariokeiD, Georg KoscheiD, Verónica Moreno‐JuaniD, Alexandra C. Brignall, Tiago Martins RodriguesiD, Alexandra Graff-MeyeriD, Talia UlmeriD, Stephanie Haeuselmann, Dinko PavlinićiD, Nicole Ledergerber, Brigitte Gross Scherf, Balázs József RózsaiD, Jacek KróliD, Simone PicelliiD, Cameron S. CowaniD, Botond RoskaiD
Abstract
Cortical circuits are composed predominantly of pyramidal-to-pyramidal neuron connections, yet their assembly during embryonic development is not well understood. We show that embryonic layer 5 pyramidal neurons, identified through single cell transcriptomics, display two phases of circuit assembly in vivo. At E14.5, a multi-layered circuit motif, composed of a single layer 5 cell type, forms. This motif is transient, switching to a second circuit motif, involving all three types, by E17.5. In vivo targeted single cell recordings and two-photon calcium imaging of embryonic layer 5 neurons reveal that, in both phases, neurons have active somas and neurites, tetrodotoxin-sensitive voltage-gated conductances, and functional glutamatergic synapses. Embryonic layer 5 neurons strongly express autism-associated genes, and perturbing these genes disrupts the switch between the two motifs. Hence, layer 5 pyramidal neurons form transient active pyramidal-to-pyramidal circuits, at the inception of neocortex, and studying these circuits could yield insights into the etiology of autism.
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