Evidence map›Paper›PMID 41474071›Full record

ArticleSmall (Weinheim an der Bergstrasse, Germany)2026

Heart-On-a-Chip with Integrated Ultrasoft Mechanosensors for Continuous Measurement of Cell- and Tissue-Scale Contractile Stresses.

Ali Mousavi, Christina-Marie Boghdady, Shihao Cui, Sabra Rostami, Amid Shakeri, Naimeh Rafatian, Mark Aurousseau, Gregor Andelfinger, Milica Radisic, Christopher Moraes and 1 more

Abstract read
In one paragraph

Article in Small (Weinheim an der Bergstrasse, Germany), 2026. 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. Review
  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

11 authors.

Ali MousaviInstitute of Biomedical Engineering, Department of Pharmacology and Physiology, Faculty of Medicine, Université de Montréal, Montréal, QC, Canada.
Christina-Marie BoghdadyDepartment of Chemical Engineering, McGill University, Montréal, QC, Canada.
Shihao CuiCHU Sainte-Justine Research Center, Montréal, QC, Canada.
Sabra RostamiDepartment of Chemical Engineering, McGill University, Montréal, QC, Canada.
Amid ShakeriInstitute of Biomedical Engineering, University of Toronto, Toronto, ON, Canada.
Naimeh RafatianCHU Sainte-Justine Research Center, Montréal, QC, Canada.
Mark AurousseaueNUVIO Inc., Montréal, QC, Canada.
Gregor AndelfingerCHU Sainte-Justine Research Center, Montréal, QC, Canada.
Milica RadisicInstitute of Biomedical Engineering, University of Toronto, Toronto, ON, Canada.
Christopher MoraesDepartment of Chemical Engineering, McGill University, Montréal, QC, Canada.
Houman SavojiInstitute of Biomedical Engineering, Department of Pharmacology and Physiology, Faculty of Medicine, Université de Montréal, Montréal, QC, Canada.ORCID 0000-0002-5596-673X

Funding

Fonds de Recherche du Québec Santé (FRQS) ResearchScholarJ1(313837)Montréal TransMedTech Institute (iTMT)Natural Sciences and Engineering Research Council of Canada DGECR-2021-00337Natural Sciences and Engineering Research Council of Canada RGPIN-2021-03960Natural Sciences and Engineering Research Council of Canada RGPIN-2022-05165Wellcome Trust 324277
6 · The paper itself

Abstract

Heart-on-a-chip platforms aim to recapitulate cardiac tissue structure and function in vitro. Traditionally, microfabricated pillars are used to estimate contractile forces based on pillar deflection. However, this approach measures only global forces at the pillar interface and lacks the spatial resolution needed to capture local mechanical stresses. In this study, we present a non-destructive optical method for continuous, multi-scale stress mapping using ultrasoft edge-labeled micro-spherical stress gauges (eMSGs). These embedded mechanosensors visibly deform in response to cellular and extracellular matrix (ECM)-generated stresses, enabling real-time measurements at cell and tissue scales. Our platform features dual cell-seeding chambers with flexible polydimethylsiloxane pillars, into which neonatal rat cardiomyocytes are seeded within a fibrin/Geltrex hydrogel containing eMSGs. Over time, tissues compacted, aligned, and exhibited spontaneous contractions and calcium transients. By modulating ECM composition, we found that reduced fibrin concentration enhanced contractile frequency, regularity, and force generation. Analysis of eMSG deformation enabled calculation of lateral and longitudinal stresses, revealing the impact of compaction and contraction on local mechanics. Finally, drug testing was performed using norepinephrine, which enhanced contractile force, and blebbistatin, which inhibited contraction, demonstrating robust pharmacological responsiveness. This platform provides a powerful tool for real-time biomechanical analysis and drug testing in engineered cardiac tissues.

Indexed as

Lab-On-A-Chip DevicesMyocardial ContractionStress, MechanicalAnimalsDimethylpolysiloxanesExtracellular MatrixMyocytes, CardiacRatsDimethylpolysiloxanescell‐generated stressescontractilitydrug screeningheart‐on‐a‐chipultrasoft mechanosensors

Identifiers

PMID41474071
PMCPMC12895230

What OpenQuestion holds

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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.