Evidence map›Paper›PMID 39558452›Full record

ArticleThe Journal of physiology2024

Purkinje cell ablation and Purkinje cell-specific deletion of Tsc1 in the developing cerebellum strengthen cerebellothalamic synapses.

Hiroshi Nishiyama, Naoko Nishiyama, Boris V Zemelman

Abstract read
In one paragraph

Article in The Journal of physiology, 2024. 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

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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

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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. Brain-wide mapping of developmental trajectories of cerebellar efferent projections.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Hiroshi NishiyamaCenter for Learning and Memory, Department of Neuroscience, The University of Texas at Austin, Austin, TX, USA.ORCID 0000-0001-5034-5777
Naoko NishiyamaCenter for Learning and Memory, Department of Neuroscience, The University of Texas at Austin, Austin, TX, USA.
Boris V ZemelmanCenter for Learning and Memory, Department of Neuroscience, The University of Texas at Austin, Austin, TX, USA.

Funding

Neural ensembles underlying natural tracking behaviorU01NS094330 · NINDS · UNIVERSITY OF TEXAS AT AUSTIN · PI FIETE, ILA R., HUK, ALEXANDER C · 2015 to 2018
$3.2M
An optical-genetic toolbox for reading and writing neural population codes in functional mapsU01NS099720 · NINDS · UNIVERSITY OF TEXAS AT AUSTIN · PI GEISLER, WILSON S, SEIDEMANN, EYAL J · 2016 to 2018
$1.8M
Cerebellar contribution to thalamic developmentR21NS108252 · NINDS · UNIVERSITY OF TEXAS AT AUSTIN · PI NISHIYAMA, HIROSHI · 2019 to 2019
$420k
HHS | NIH | National Institute of Neurological Disorders and Stroke (NINDS) 1U01NS094330HHS | NIH | National Institute of Neurological Disorders and Stroke (NINDS) 1U01NS099720HHS | NIH | National Institute of Neurological Disorders and Stroke (NINDS) R21NS108252NINDS NIH HHS R21 NS108252NINDS NIH HHS U01 NS094330NINDS NIH HHS U01 NS099720
6 · The paper itself

Abstract

Cerebellar damage early in life often causes long-lasting motor, social and cognitive impairments, suggesting the roles of the cerebellum in developing a broad spectrum of behaviours. This recent finding has promoted research on how cerebellar damage affects the development of the cerebral cortex, the brain region responsible for higher-order control of all behaviours. However, the cerebral cortex is not directly connected to the cerebellum. The thalamus is a major direct target of the cerebellar nuclei, conveying cerebellar signals to the cerebral cortex. Despite its crucial position in cerebello-cerebral interaction, thalamic susceptibility to cerebellar damage remains largely unclear. Here, we studied the consequences of early cerebellar perturbation on thalamic development. Whole-cell patch-clamp recordings showed that the synaptic organization of the cerebellothlamic circuit is similar to that of the primary sensory thalamus, in which aberrant sensory activity alters synaptic circuit formation. The ablation of Purkinje cells in the developing cerebellum strengthened cerebellothalamic synapses and enhanced thalamic suprathreshold activities. Purkinje-cell specific deletion of tuberous sclerosis complex subunit 1 (Tsc1), an autism-associated gene for which the protein product negatively regulates the mammalian target of rapamycin, also strengthened cerebellothalamic synapses. However, this strengthening occurred only in homozygous deletion, whereas both homozygous and hemizygous deletion are known to cause autism-like behaviours. These results suggest that, although the cerebellothalamic projection is vulnerable to disturbances in the developing cerebellar cortex, other changes may also drive the behavioural consequences of early cerebellar perturbation. KEY POINTS: Cerebellar damage early in life often causes motor, social and cognitive impairments, suggesting the roles of the cerebellum in developing a broad spectrum of behaviours. Recent studies focus on how the developing cerebellum affects the formation and function of the cerebral cortex, the higher-order centre for all behaviours. However, the cerebellum does not directly connect to the cerebral cortex. Here, we studied the consequences of early cerebellar perturbation on the thalamus because it is a direct postsynaptic target of the cerebellum, sending cerebellar signals to the cerebral cortex. Loss of cerebellar Purkinje cells, which are commonly associated with various neurological disorders, strengthened cerebellothalamic synapses, suggesting the vulnerability of the thalamus to substantial disturbance in the developing cerebellum. Purkinje cell-specific loss of tuberous sclerosis complex-1, a negative regulator of mammalian target of rapamycin, is an established mouse model of autism. This mouse model also showed strengthened cerebellothalamic synapses.

Indexed as

CerebellumPurkinje CellsSynapsesThalamusTuberous Sclerosis Complex 1 ProteinAnimalsMaleMiceMice, Inbred C57BLMice, KnockoutTsc1 protein, mouseTuberous Sclerosis Complex 1 Proteincerebellumdevelopmentoptogeneticspurkinje cellsthalamuswhole‐cell recording

Identifiers

PMID39558452
PMCPMC11649526

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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.