Evidence map›Paper›PMID 39945052›Full record

ArticleCardiovascular research2025

Stretch regulation of β2-Adrenoceptor signalling in cardiomyocytes requires caveolae.

Jiarong Fu, Catherine Mansfield, Ivan Diakonov, Aleksandra Judina, Matthew Delahaye, Navneet Bhogal, Jose L Sanchez-Alonso, Timothy Kamp, Julia Gorelik

Abstract read
In one paragraph

Article in Cardiovascular research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Caveolae: Metabolic Platforms at the Crossroads of Health and Disease.International journal of molecular sciences · 2025
    Review
  6. Review
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

9 authors.

Jiarong FuNational Heart and Lung Institute, Imperial College London, Du Cane Road, London W12 0NN, UK.ORCID 0000-0003-4130-6746
Catherine MansfieldNational Heart and Lung Institute, Imperial College London, Du Cane Road, London W12 0NN, UK.
Ivan DiakonovNational Heart and Lung Institute, Imperial College London, Du Cane Road, London W12 0NN, UK.
Aleksandra JudinaNational Heart and Lung Institute, Imperial College London, Du Cane Road, London W12 0NN, UK.
Matthew DelahayeNational Heart and Lung Institute, Imperial College London, Du Cane Road, London W12 0NN, UK.
Navneet BhogalNational Heart and Lung Institute, Imperial College London, Du Cane Road, London W12 0NN, UK.
Jose L Sanchez-AlonsoNational Heart and Lung Institute, Imperial College London, Du Cane Road, London W12 0NN, UK.ORCID 0000-0003-2942-0079
Timothy KampCellular and Molecular Arrhythmia Research Program, Department of Medicine, University of Wisconsin, 1111 Highland Avenue, Madison, WI 53792, USA.
Julia GorelikNational Heart and Lung Institute, Imperial College London, Du Cane Road, London W12 0NN, UK.

Funding

British Heart Foundation BHF- RG/F/22/110081
6 · The paper itself

Abstract

aimsCaveolin-3 is essential for the formation of caveolae in cardiomyocytes. Caveolar microdomains have been shown to regulate the distribution of signalling proteins such as beta-adrenoceptors (βAR) and may act as membrane reserves to protect the cell from damage during the mechanical stretch. Myocardial stretch occurs during haemodynamic overload and may be normal (e.g. exercise) or pathological (e.g. heart failure); therefore, it is important to understand the effect of stretch on signalling pathways associated with mechanosensitive structures, such as caveolae. In this study, we investigate the role of caveolae in regulating the effect of stretch on βAR-signalling. METHODS AND

resultsWe used osmotic swelling of isolated rat ventricular cardiomyocytes as a method to stretch the cell membrane and investigate the effect of βAR stimulation on cyclic adenosine monophosphate (cAMP) activity and contractility. βAR response was measured using a Förster Resonance Energy Transfer reporter for the second messenger cAMP and using CytoCypher for the measurement of cell contractility. β1AR and β2AR blockers were used to selectively allow stimulation of β2AR and β1AR, respectively. We also investigated the effect of stretch on βAR response to isoprenaline stimulation in left ventricular trabeculae dissected from control and cardiac-specific caveolin-3 knock-out mice (Cav3KO). Stretching trabeculae produces increased baseline adenylyl cyclase activity and a higher level of cAMP and a greater β2AR-induced positive inotropy after stimulation of the β2AR but not β1AR, by isoprenaline. Similar findings were confirmed for isolated myocytes subjected to hypoosmotic conditions. In isolated cardiomyocytes, caveolae depletion using methyl-beta-cyclodextrin or Cav3KO abolished the increase in β2AR response induced by stretch.

conclusionOur study reveals a stretch-regulation of the β2AR signalling pathway, which requires functional caveolae. This indicates caveolae are mechanosensitive membrane domains that undergo structural and functional changes in response to stretch, thus leading to mechanical regulation of caveolae-associated signalling pathways.

Indexed as

CaveolaeMechanotransduction, CellularMyocardial ContractionMyocytes, CardiacReceptors, Adrenergic, beta-2Adrenergic beta-2 Receptor AgonistsAnimalsCaveolin 3Cells, CulturedCyclic AMPIsolated Heart PreparationIsoproterenolMaleMiceMice, Inbred C57BLMice, KnockoutAdrb1 protein, ratAdrb2 protein, ratAdrenergic beta-2 Receptor AgonistsCav3 protein, mouseCav3 protein, ratCaveolin 3Cyclic AMPIsoproterenolReceptors, Adrenergic, beta-1Receptors, Adrenergic, beta-2Beta-2-AdrenoceptorCardiacCaveolaeCaveolin-3Stretch

Identifiers

PMID39945052
PMCPMC12038227

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LicenceCC BY-NC
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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.