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Higher-order thalamocortical circuits are specified by embryonic cortical progenitor types in the mouse brain

Abstract:
The sensory cortex receives synaptic inputs from both first-order and higher-order thalamic nuclei. First-order inputs relay simple stimulus properties from the periphery, whereas higher-order inputs relay more complex response properties, provide contextual feedback, and modulate plasticity. Here, we reveal that a cortical neuron’s higher-order input is determined by the type of progenitor from which it is derived during embryonic development. Within layer 4 (L4) of the mouse primary somatosensory cortex, neurons derived from intermediate progenitors receive stronger higher-order thalamic input and exhibit greater higher-order sensory responses. These effects result from differences in dendritic morphology and levels of the transcription factor Lhx2, which are specified by the L4 neuron’s progenitor type. When this mechanism is disrupted, cortical circuits exhibit altered higher-order responses and sensory-evoked plasticity. Therefore, by following distinct trajectories, progenitor types generate diversity in thalamocortical circuitry and may provide a general mechanism for differentially routing information through the cortex.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1016/j.celrep.2024.114157

Authors


More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Pharmacology
Role:
Author
ORCID:
0000-0002-6378-5015
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Pharmacology
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Pharmacology
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Pharmacology
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Pharmacology
Role:
Author


More from this funder
Funder identifier:
https://ror.org/0472cxd90
Grant:
617670
More from this funder
Funder identifier:
https://ror.org/00cwqg982
Grant:
BB/S007938/1


Publisher:
Cell Press
Journal:
Cell Reports More from this journal
Volume:
43
Issue:
5
Article number:
114157
Place of publication:
United States
Publication date:
2024-04-26
Acceptance date:
2024-04-10
DOI:
EISSN:
2211-1247
ISSN:
2639-1856
Pmid:
38678557


Language:
English
Keywords:
Pubs id:
1994091
Local pid:
pubs:1994091
Deposit date:
2024-09-18

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