Evidence map›Paper›PMID 41872887›Full record

ArticleSkeletal muscle2026

CtBP1 sustains activity-dependent muscle properties and dampens synaptic, contractile and metabolic changes triggered by denervation.

Olivia Cattaneo, Gaetan Lopez, Jayasimman Rajendran, Florent Chabry, Nicolas Liaudet, Sergei Startchik, Alexandre Prola, Perrine Castets

Abstract read
In one paragraph

Article in Skeletal muscle, 2026. 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

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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

2 citing papers in PubMed.

  1. Review
  2. Delineating theInternational journal of molecular sciences · 2026
    Review
4 · The record

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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.

Olivia CattaneoDepartment of Cell Physiology and Metabolism, Faculty of Medicine, University of Geneva, Geneva, CH-1211, Switzerland.
Gaetan Lopez *Department of Cell Physiology and Metabolism, Faculty of Medicine, University of Geneva, Geneva, CH-1211, Switzerland.
Jayasimman Rajendran *Department of Cell Physiology and Metabolism, Faculty of Medicine, University of Geneva, Geneva, CH-1211, Switzerland.
Florent ChabryDepartment of Cell Physiology and Metabolism, Faculty of Medicine, University of Geneva, Geneva, CH-1211, Switzerland.
Nicolas LiaudetBioimaging Core Facility, Faculty of Medicine, University of Geneva, Geneva, 1211, Switzerland.
Sergei StartchikBioimaging Core Facility, Faculty of Medicine, University of Geneva, Geneva, 1211, Switzerland.
Alexandre ProlaDepartment of Cell Physiology and Metabolism, Faculty of Medicine, University of Geneva, Geneva, CH-1211, Switzerland.
Perrine CastetsDepartment of Cell Physiology and Metabolism, Faculty of Medicine, University of Geneva, Geneva, CH-1211, Switzerland. perrine.castets@unige.ch.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDenervation triggers dramatic atrophy of skeletal muscle, accompanied by synaptic, contractile and metabolic changes. Several factors were shown to contribute to genetic reprogramming and proteostasis changes after denervation. However, the mechanisms underlying the coordinated regulation of denervation-induced muscle fiber remodeling remain misunderstood.

methodsWe investigated the role of the transcriptional co-repressor CtBP1 in the regulation of denervation-induced responses in muscle fibers. To this end, we analyzed its expression and localization in innervated and denervated muscles and assessed the consequences of its knockdown induced in vivo with AAV9, on synaptic, contractile and metabolic properties of muscle fibers.

resultsCtBP1 was present both in sub- and non-synaptic myonuclei in innervated muscle. Although CtBP1 levels remained unchanged in denervated muscle, CtBP1 accumulated transiently in myonuclei after 2 days of denervation in TA/EDL muscles. Ctbp1 knockdown perturbed the expression of a large set of activity-independent and -dependent genes in innervated and denervated skeletal muscles. Reducing CtBP1 levels had limited effect on the expression of most synaptic genes, but increased transcript levels of Chrne, encoding the adult ε sub-unit of acetylcholine receptors (AChR). However, it did not affect AChR turnover or maintenance of the post-synaptic compartment upon denervation. Importantly, we uncovered that Ctbp1 knockdown exacerbates denervation-induced changes in metabolic gene expression, including most genes encoding proteins of the respiratory chain complexes. Consistently, it induced a contractile shift towards slower fibers in innervated fast muscle, mimicking denervation, and enhanced the denervation-induced metabolic transition towards oxidative slow-twitch fibers. Moreover, Ctbp1 knockdown precipitated the profound ultrastructural remodeling of mitochondria network induced after denervation.

conclusionsOur study unveils that CtBP1 sustains the innervated muscle pattern and antagonizes the effect of denervation on synaptic, contractile and metabolic muscle properties, with important implications for CtBP1-related muscle diseases.

Indexed as

Alcohol OxidoreductasesDNA-Binding ProteinsMuscle ContractionMuscle DenervationMuscle, SkeletalSynapsesAnimalsMaleMiceMice, Inbred C57BLAlcohol OxidoreductasesC-terminal binding proteinDNA-Binding ProteinsCtBP1DenervationFiber typeMetabolismMitochondriaSkeletal muscle

Identifiers

PMID41872887
PMCPMC13130457

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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 Socratic graph.