Evidence map›Paper›PMID 40753314›Full record

ArticleMolecular neurobiology2025

Knock-out of Tpm4.2/Actin Filaments Alters Neuronal Signaling, Neurite Outgrowth, and Behavioral Phenotypes in Mice.

Sian Genoud, Chanchanok Chaichim, Rossana Rosa Porto, Tamara Tomanic, Holly Stefen, Esmeralda Paric, Soumalya Sarkar, Dasol Yoo, Wendi Gao, Edna C Hardeman and 4 more

Abstract read
In one paragraph

Article in Molecular neurobiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

14 authors.

Sian Genoud *Faculty of Medicine, Macquarie Medical School, Dementia Research Centre, Macquarie University, Health & Human Sciences, Sydney, NSW, 2109, Australia.
Chanchanok Chaichim *School of Medical Sciences, University of New South Wales, Sydney, NSW, 2052, Australia.
Rossana Rosa Porto *School of Medicine, Western Sydney University, Campbelltown, NSW, 2560, Australia.
Tamara TomanicFaculty of Medicine, Macquarie Medical School, Dementia Research Centre, Macquarie University, Health & Human Sciences, Sydney, NSW, 2109, Australia.
Holly StefenFaculty of Medicine, Macquarie Medical School, Dementia Research Centre, Macquarie University, Health & Human Sciences, Sydney, NSW, 2109, Australia.
Esmeralda ParicFaculty of Medicine, Macquarie Medical School, Dementia Research Centre, Macquarie University, Health & Human Sciences, Sydney, NSW, 2109, Australia.
Soumalya SarkarFaculty of Medicine, Macquarie Medical School, Dementia Research Centre, Macquarie University, Health & Human Sciences, Sydney, NSW, 2109, Australia.
Dasol YooFaculty of Medicine, Macquarie Medical School, Dementia Research Centre, Macquarie University, Health & Human Sciences, Sydney, NSW, 2109, Australia.
Wendi GaoSchool of Medical Sciences, University of New South Wales, Sydney, NSW, 2052, Australia.
Edna C HardemanSchool of Medical Sciences, University of New South Wales, Sydney, NSW, 2052, Australia.
Peter W GunningSchool of Medical Sciences, University of New South Wales, Sydney, NSW, 2052, Australia.
Tim KarlSchool of Medicine, Western Sydney University, Campbelltown, NSW, 2560, Australia.
John Power *School of Medical Sciences, University of New South Wales, Sydney, NSW, 2052, Australia.
Thomas Fath *Faculty of Medicine, Macquarie Medical School, Dementia Research Centre, Macquarie University, Health & Human Sciences, Sydney, NSW, 2109, Australia. Thomas.fath@mq.edu.au.

Funding

Australian Research Council DP180101473National Health and Medical Research Council APP1083209
6 · The paper itself

Abstract

Tropomyosins (Tpm) are master regulators of actin dynamics through forming co-polymers with filamentous actin. Despite the well-understood function of muscle Tpms in the contractile apparatus of muscle cells, much less is known about the diverse physiological function of cytoplasmic Tpms in eukaryotic cells. Here, we investigated the role of the Tpm4.2 isoform in neuronal processes including signaling, neurite outgrowth, and receptor recycling using primary neurons from Tpm4.2 knock-out mice. Live imaging of calcium and electrophysiology data demonstrated increased frequency, yet reduced strength of single neuron spikes. Calcium imaging further showed an increase in neuronal networks. In vitro assays of Tpm4.2 knock-out neurons displayed impaired recycling of the AMPA neurotransmitter receptor subunit GluA1. Morphometric analysis of neurite growth showed increased dendritic complexity and altered dendritic spine morphology in Tpm4.2 knock-out primary neurons. Behavioral analysis of Tpm4.2 knock-out mice displayed heightened anxiety in the open field test, while the elevated plus maze displayed heightened anxiety only in females. Our study depicts the multi-faceted role of the Tpm4.2 isoform and its co-polymer F-actin population in neurons, with potential implications for better understanding diseases of the nervous system which involve actin cytoskeleton dysfunction.

Indexed as

Actin CytoskeletonBehavior, AnimalNeuritesNeuronal OutgrowthNeuronsSignal TransductionTropomyosinAnimalsAnxietyCells, CulturedDendritic SpinesFemaleMaleMiceMice, Inbred C57BLMice, KnockoutProtein IsoformsReceptors, AMPATropomyosinActin cytoskeletonNeuronal signalingNeuronsTyopomyosin

Identifiers

PMID40753314
PMCPMC12559059

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.