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Granularity of thalamic head direction cells

Abstract:
Head direction signaling is fundamental for spatial orientation and navigation. The anterodorsal nucleus of the thalamus (ADn) contains a high density of head direction (HD) cells that process sensorimotor inputs for subsequent synaptic integration in postsynaptic cortical areas. We tested the hypothesis that individual HD cells show differences in their firing patterns and connectivity by recording and juxtacellularly labeling single HD cells in subregions of the ADn in awake mice during passive rotation. We identified HD cells that exhibited different response profiles to light, sound, and movement. We also identified a mediolateral gradient of calretinin-expressing (CR+) ADn cells, with CR+ HD cells having narrower tuning widths, lower maximal firing rates, and different intrinsic properties compared to CR-cells. Axons of labeled HD cells could be followed to the retrosplenial cortex, with collaterals innervating the thalamic reticular nucleus (type I cells); others additionally innervated the dorsomedial striatum (type II cells). Most medial CR+ cells preferentially projected to ventral retrohippocampal regions. Surprisingly, we also identified a subpopulation of medial CR+ cells with twisted dendrites and descending axons that avoided the thalamic reticular nucleus, termed tortuosa HD cells (type III cells). We conclude that HD cells of the mouse ADn comprise distinct cell types, providing parallel head-direction-modulated sensorimotor messages to synaptic target neurons within the head direction network.
Publication status:
Published
Peer review status:
Not peer reviewed

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Preprint server copy:
10.1101/2025.09.08.674912

Authors

More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Pharmacology
Oxford college:
Linacre College
Role:
Author
ORCID:
0000-0002-1754-283X
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Pharmacology
Role:
Author
ORCID:
0000-0003-1265-4776
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Pharmacology
Role:
Author
ORCID:
0009-0007-5160-6810
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Pharmacology
Role:
Author


More from this funder
Funder identifier:
https://ror.org/03x94j517
Grant:
MR/R011567/1
MR/Z504518/1
More from this funder
Funder identifier:
https://ror.org/001aqnf71
Grant:
EP/Z001358/1
More from this funder
Funder identifier:
https://ror.org/00rk2pe57


Preprint server:
bioRxiv
Publication date:
2025-09-14
DOI:


Language:
English
Pubs id:
2293159
Local pid:
pubs:2293159
Deposit date:
2025-10-20
ARK identifier:

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