Evidence map›Paper›PMID 40782799›Full record

ArticleNeuron2025

Direction-selective laterodorsal thalamic nucleus encodes optic flow and turning in spatial navigation.

Zhong Li, Junxiang J Huang, Yuan E Zhang, Kaixin K Su, Bo Peng, Boyoon M Seo, Li I Zhang, Huizhong Whit Tao

Abstract read
In one paragraph

Article in Neuron, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Zhong LiCenter for Neural Circuits and Sensory Processing Disorders, Zilkha Neurogenetic Institute, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA. Electronic address: zli@usc.edu.
Junxiang J HuangCenter for Neural Circuits and Sensory Processing Disorders, Zilkha Neurogenetic Institute, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA; Graduate Program in Biomedical and Biological Sciences, University of Southern California, Los Angeles, CA 90033, USA.
Yuan E ZhangCenter for Neural Circuits and Sensory Processing Disorders, Zilkha Neurogenetic Institute, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA.
Kaixin K SuCenter for Neural Circuits and Sensory Processing Disorders, Zilkha Neurogenetic Institute, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA; Graduate Program in Biomedical and Biological Sciences, University of Southern California, Los Angeles, CA 90033, USA.
Bo PengCenter for Neural Circuits and Sensory Processing Disorders, Zilkha Neurogenetic Institute, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA; Graduate Program in Neuroscience, University of Southern California, Los Angeles, CA 90033, USA.
Boyoon M SeoCenter for Neural Circuits and Sensory Processing Disorders, Zilkha Neurogenetic Institute, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA; Graduate Program in Neuroscience, University of Southern California, Los Angeles, CA 90033, USA.
Li I ZhangCenter for Neural Circuits and Sensory Processing Disorders, Zilkha Neurogenetic Institute, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA; Department of Physiology & Neuroscience, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA. Electronic address: liizhang@usc.edu.
Huizhong Whit TaoCenter for Neural Circuits and Sensory Processing Disorders, Zilkha Neurogenetic Institute, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA; Department of Physiology & Neuroscience, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA. Electronic address: htao@usc.edu.

Funding

Cell atlas of mouse brain-spinal cord connectomeU01MH116990 · NIMH · UNIVERSITY OF SOUTHERN CALIFORNIA · PI DONG, HONG-WEI, TAO, HUIZHONG WHIT · 2018 to 2022
$12.0M
Processing and transformation of visual signals in the superior colliculusR01EY019049 · NEI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI TAO, HUIZHONG WHIT · 2008 to 2025
$9.2M
Thalamic Modulation of Auditory Cortical Processing via LPR01DC008983 · NIDCD · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Li I Zhang · 2007 to 2026
$8.7M
Understanding Neural Bases for Neuropsychiatric Impairments in Alzheimer's Disease ModelsR01AG089756 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Huizhong Whit Tao, Zhen Zhao · 2024 to 2026
$3.6M
Neural circuits for social modulation of a persistent negative emotional stateRF1NS132912 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI HONG, WEIZHE, ZHANG, LI I · 2023 to 2023
$3.2M
Cell-type basis for auditory processing in the inferior colliculusR01DC020887 · NIDCD · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Li I Zhang · 2023 to 2026
$2.2M
NEI NIH HHS R01 EY019049NIA NIH HHS R01 AG089756NIDCD NIH HHS R01 DC008983NIDCD NIH HHS R01 DC020887NIMH NIH HHS U01 MH116990NINDS NIH HHS RF1 NS132912
6 · The paper itself

Abstract

Vision is crucial for efficient navigation, but how the brain transforms visual signals into navigational cues remains unclear. The laterodorsal thalamic nucleus (LD), with strong connections to visual and navigation circuits, is well positioned for this function, yet its role has been largely unexplored. In mice, we found that LD neurons exhibit strong direction selectivity, with a dominant directional preference for contralateral-to-ipsilateral visual motion, mirroring horizontal optic flow during contraversive turning. In freely moving animals, LD ensembles were preferentially activated during contraversive rather than ipsiversive turns in a vision-dependent manner, enabling the encoding of turning direction. Optogenetic activation or suppression of LD during learned navigational tasks selectively biased turning decisions in accordance with its directional preference. These findings suggest that by converting visual motion into egocentric turning cues, LD may serve as a critical hub linking vision to navigation and contribute to spatial cognition and memory.

Indexed as

NeuronsOptic FlowSpatial NavigationThalamic NucleiAnimalsCuesMaleMiceMice, Inbred C57BLMotion PerceptionOptogeneticsdirection selectivityegocentric navigationhigher-order thalamuslateral dorsal nucleusoptic flowspatial learningspatial memorysubiculumvisual cortexvisual motion

Identifiers

PMID40782799
PMCPMC13186451

What OpenQuestion holds

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Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.