Evidence map›Paper›PMID 34019719›Full record

ArticleBiotechnology and bioengineering2021

Assessing the influence of perfusion on cardiac microtissue maturation: A heart-on-chip platform embedding peristaltic pump capabilities.

Daniela Cruz-Moreira, Roberta Visone, Francisco Vasques-Nóvoa, António S Barros, Adelino Leite-Moreira, Alberto Redaelli, Matteo Moretti, Marco Rasponi

Open access · hybridAbstract read
In one paragraph

Article in Biotechnology and bioengineering, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

22 citing papers in PubMed, 29 citations in OpenAlex.

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  7. Engineering in vitro vascular microsystems.Microsystems & nanoengineering · 2025
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  8. Article
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  13. Advances in the Model Structure of In Vitro Vascularized Organ-on-a-Chip.Cyborg and bionic systems (Washington, D.C.) · 2024
    Article
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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

8 authors at 3 institutions in 3 countries.

Daniela Cruz-MoreiraDepartment of Electronics, Information and Bioengineering, Politecnico di Milano, Milano, Italy.ORCID 0000-0003-0868-7372
Roberta VisoneDepartment of Electronics, Information and Bioengineering, Politecnico di Milano, Milano, Italy.ORCID 0000-0001-9077-1922
Francisco Vasques-NóvoaCardiovascular Research and Development Center, Faculty of Medicine, University of Porto, Porto, Portugal.ORCID 0000-0003-0509-2146
António S BarrosCardiovascular Research and Development Center, Faculty of Medicine, University of Porto, Porto, Portugal.ORCID 0000-0002-9103-5852
Adelino Leite-MoreiraCardiovascular Research and Development Center, Faculty of Medicine, University of Porto, Porto, Portugal.ORCID 0000-0001-7808-3596
Alberto RedaelliDepartment of Electronics, Information and Bioengineering, Politecnico di Milano, Milano, Italy.ORCID 0000-0002-9020-2188
Matteo MorettiCell and Tissue Engineering Laboratory, IRCCS Istituto Ortopedico Galeazzi, Milan, Italy.ORCID 0000-0002-7301-1208
Marco RasponiDepartment of Electronics, Information and Bioengineering, Politecnico di Milano, Milano, Italy.ORCID 0000-0002-2904-8652
Politecnico di Milano · ITUniversidade do Porto · PTEnte Ospedaliero Cantonale · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Heart-on-chip is an unprecedented technology for recapitulating key biochemical and biophysical cues in cardiac pathophysiology. Several designs have been proposed to improve its ability to mimic the native tissue and establish it as a reliable research platform. However, despite mimicking one of most vascularized organs, reliable strategies to deliver oxygen and substrates to densely packed constructs of metabolically demanding cells remain unsettled. Herein, we describe a new heart-on-chip platform with precise fluid control, integrating an on-chip peristaltic pump, allowing automated and fine control over flow on channels flanking a 3D cardiac culture. The application of distinct flow rates impacted on temporal dynamics of microtissue structural and transcriptional maturation, improving functional performance. Moreover, a widespread transcriptional response was observed, suggesting flow-mediated activation of critical pathways of cardiomyocyte structural and functional maturation and inhibition of cardiomyocyte hypoxic injury. In conclusion, the present design represents an important advance in bringing engineered cardiac microtissues closer to the native heart, overcoming traditional bulky off-chip fluid handling systems, improving microtissue performance, and matching oxygen and energy substrate requirements of metabolically active constructs, avoiding cellular hypoxia. Distinct flow patterns differently impact on microtissue performance and gene expression program.

Indexed as

Infusion PumpsLab-On-A-Chip DevicesPerfusionAnimalsCell HypoxiaMyocardiumMyocytes, CardiacRatsRats, Sprague-DawleyTissue Culture Techniquesheartheart-on-chipmaturationmechanotransductionperfusion

Identifiers

PMID34019719
PMCPMC8362142
OpenAlexW3162726641

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.