Evidence map›Paper›PMID 35139328›Full record

ReviewJournal of molecular and cellular cardiology2022

The harder the climb the better the view: The impact of substrate stiffness on cardiomyocyte fate.

Silvia Querceto, Rosaria Santoro, Aoife Gowran, Bruno Grandinetti, Giulio Pompilio, Michael Regnier, Chiara Tesi, Corrado Poggesi, Cecilia Ferrantini, Josè Manuel Pioner

Open access · bronzeAbstract readReview
In one paragraph

Review in Journal of molecular and cellular cardiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
5.2field-weighted citation impact, top 4% of its field
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

21 citing papers in PubMed, 27 citations in OpenAlex.

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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

10 authors at 5 institutions in 2 countries.

Silvia QuercetoDivision of Physiology, Department of Experimental and Clinical Medicine, Università degli Studi di Firenze, Florence, Italy.
Rosaria SantoroUnità di Biologia Vascolare e Medicina Rigenerativa, Centro Cardiologico Monzino IRCCS, via Carlo Parea 4, Milan, Italy; Department of Electronics, Information and Biomedical Engineering, Politecnico di Milano, Milan, Italy.
Aoife GowranUnità di Biologia Vascolare e Medicina Rigenerativa, Centro Cardiologico Monzino IRCCS, via Carlo Parea 4, Milan, Italy.
Bruno GrandinettiEuropean Laboratory for Non-Linear Spectroscopy (LENS), Sesto Fiorentino, FI, Italy.
Giulio PompilioUnità di Biologia Vascolare e Medicina Rigenerativa, Centro Cardiologico Monzino IRCCS, via Carlo Parea 4, Milan, Italy; Department of Biomedical, Surgical and Dental Sciences, University of Milan, Italy.
Michael RegnierDepartment of Bioengineering, University of Washington, Seattle, WA, USA.
Chiara TesiDivision of Physiology, Department of Experimental and Clinical Medicine, Università degli Studi di Firenze, Florence, Italy.
Corrado PoggesiDivision of Physiology, Department of Experimental and Clinical Medicine, Università degli Studi di Firenze, Florence, Italy.
Cecilia FerrantiniDivision of Physiology, Department of Experimental and Clinical Medicine, Università degli Studi di Firenze, Florence, Italy.
Josè Manuel PionerDepartment of Biology, Università degli Studi di Firenze, Florence, Italy. Electronic address: josemanuel.pioner@unifi.it.
University of Florence · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITPolitecnico di Milano · ITUniversity of Milan · ITUniversity of Washington · US

Funding

From proteins to cells to tissues: A multi-scale assessment of biomechanical regulation by the myosin molecular motorRM1GM131981 · NIGMS · STANFORD UNIVERSITY · PI BERNSTEIN, DANIEL, MACK, DAVID LEE · 2019 to 2023
$10.3M
UW Center for Translational Muscle Research (Overall Application)P30AR074990 · NIAMS · UNIVERSITY OF WASHINGTON · PI Jennifer Michelle Davis, DANIEL RAFTERY · 2019 to 2026
$7.5M
Engineered Stem Cells for Cardiac RepairR01HL128368 · NHLBI · UNIVERSITY OF WASHINGTON · PI REGNIER, MICHAEL · 2018 to 2025
$6.1M
NHLBI NIH HHS R01 HL128368NIAMS NIH HHS P30 AR074990NIGMS NIH HHS RM1 GM131981
6 · The paper itself

Abstract

The quest for novel methods to mature human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) for cardiac regeneration, modelling and drug testing has emphasized a need to create microenvironments with physiological features. Many studies have reported on how cardiomyocytes sense substrate stiffness and adapt their morphological and functional properties. However, these observations have raised new biological questions and a shared vision to translate it into a tissue or organ context is still elusive. In this review, we will focus on the relevance of substrates mimicking cardiac extracellular matrix (cECM) rigidity for the understanding of the biomechanical crosstalk between the extracellular and intracellular environment. The ability to opportunely modulate these pathways could be a key to regulate in vitro hiPSC-CM maturation. Therefore, both hiPSC-CM models and substrate stiffness appear as intriguing tools for the investigation of cECM-cell interactions. More understanding of these mechanisms may provide novel insights on how cECM affects cardiac cell function in the context of genetic cardiomyopathies.

Indexed as

Induced Pluripotent Stem CellsMyocytes, CardiacCell CommunicationCell DifferentiationExtracellular MatrixHumansCardiac extracellular matrixCardiomyocytesGenetic cardiomyopathyhiPSCSubstrate stiffnessTissue engineering

Identifiers

PMID35139328
PMCPMC11270945
OpenAlexW4210760020

What OpenQuestion holds

Textmetadata
LicenceTDM
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.