Literature DB >> 30679375

Distinct molecular programs regulate synapse specificity in cortical inhibitory circuits.

Emilia Favuzzi1,2,3, Rubén Deogracias1,2,3, André Marques-Smith1,2, Patricia Maeso1,2,3, Julie Jezequel1,2, David Exposito-Alonso1,2, Maddalena Balia1,2, Tim Kroon1,2, Antonio J Hinojosa1,2,3, Elisa F Maraver1,2, Beatriz Rico4,2,3.   

Abstract

How neuronal connections are established and organized into functional networks determines brain function. In the mammalian cerebral cortex, different classes of GABAergic interneurons exhibit specific connectivity patterns that underlie their ability to shape temporal dynamics and information processing. Much progress has been made toward parsing interneuron diversity, yet the molecular mechanisms by which interneuron-specific connectivity motifs emerge remain unclear. In this study, we investigated transcriptional dynamics in different classes of interneurons during the formation of cortical inhibitory circuits in mouse. We found that whether interneurons form synapses on the dendrites, soma, or axon initial segment of pyramidal cells is determined by synaptic molecules that are expressed in a subtype-specific manner. Thus, cell-specific molecular programs that unfold during early postnatal development underlie the connectivity patterns of cortical interneurons.
Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works.

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Year:  2019        PMID: 30679375     DOI: 10.1126/science.aau8977

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  39 in total

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9.  Loss of Clustered Protocadherin Diversity Alters the Spatial Distribution of Cortical Interneurons in Mice.

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10.  A Composite Sketch of Fast-Spiking Parvalbumin-Positive Neurons.

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