| Literature DB >> 31027966 |
Jason C Wester1, Vivek Mahadevan1, Christopher T Rhodes2, Daniela Calvigioni3, Sanan Venkatesh2, Dragan Maric4, Steven Hunt1, Xiaoqing Yuan1, Yajun Zhang2, Timothy J Petros2, Chris J McBain5.
Abstract
Neocortical circuits consist of stereotypical motifs that must self-assemble during development. Recent evidence suggests that the subtype identity of both excitatory projection neurons (PNs) and inhibitory interneurons (INs) is important for this process. We knocked out the transcription factor Satb2 in PNs to induce those of the intratelencephalic (IT) type to adopt a pyramidal tract (PT)-type identity. Loss of IT-type PNs selectively disrupted the lamination and circuit integration of INs derived from the caudal ganglionic eminence (CGE). Strikingly, reprogrammed PNs demonstrated reduced synaptic targeting of CGE-derived INs relative to controls. In control mice, IT-type PNs targeted neighboring CGE INs, while PT-type PNs did not in deep layers, confirming this lineage-dependent motif. Finally, single-cell RNA sequencing revealed that major CGE IN subtypes were conserved after loss of IT PNs, but with differential transcription of synaptic proteins and signaling molecules. Thus, IT-type PNs influence CGE-derived INs in a non-cell-autonomous manner during cortical development. Published by Elsevier Inc.Entities:
Keywords: circuits; cortex; development; embryonic lineage; interneuron; projection neuron; radial migration; single-cell RNA-sequencing; synaptic physiology
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Year: 2019 PMID: 31027966 PMCID: PMC8965597 DOI: 10.1016/j.neuron.2019.03.036
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173