Evidence map›Paper›PMID 41550615›Full record

ArticleAdvanced functional materials2025

Crossbow Bioreactors for Studying the Effects of Time-Varying Mechanical Preload and Afterload on Engineered Cardiac Tissues.

Abbigail Helfer, Nicholas Strash, Marisa Patsy, Nenad Bursac

Abstract read
In one paragraph

Article in Advanced functional materials, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Abbigail HelferDepartment of Biomedical Engineering, Duke University, NC 27708.
Nicholas StrashDepartment of Biomedical Engineering, Duke University, NC 27708.
Marisa PatsyDepartment of Biomedical Engineering, Duke University, NC 27708.
Nenad BursacDepartment of Biomedical Engineering, Duke University, NC 27708.

Funding

Project 3 - Role of Proline Metabolism in Regulation of Mammalian Cardiomyocyte ProliferationP01HL160476 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Hesham Sadek · 2022 to 2026
$13.1M
Integrated Cellular and Tissue Engineering for Ischemic Heart DiseaseU01HL134764 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BURSAC, NENAD, KAMP, TIMOTHY J. · 2016 to 2022
$7.7M
Exploring the role of ATP1A3 mutations in sudden unexplained death in epilepsyR01HL160654 · NHLBI · DUKE UNIVERSITY · PI Andrew P. Landstrom · 2022 to 2026
$3.4M
Engineering Human Heart Tissues with Polyploid CardiomyocytesR01HL164013 · NHLBI · DUKE UNIVERSITY · PI BURSAC, NENAD · 2022 to 2025
$2.2M
Engineered BacNav and BacCav for Improved Excitability and ContractionR01EB032726 · NIBIB · DUKE UNIVERSITY · PI BURSAC, NENAD · 2022 to 2025
$1.9M
NHLBI NIH HHS P01 HL160476NHLBI NIH HHS R01 HL160654NHLBI NIH HHS R01 HL164013NHLBI NIH HHS U01 HL134764NIBIB NIH HHS R01 EB032726
6 · The paper itself

Abstract

Mechanical loading plays a critical role in heart development and function, with cardiac preload (tissue stretch during chamber filling) and afterload (resistance against which the heart works to eject blood) potentially playing distinct roles in postnatal cardiomyocyte maturation. To dissect the effects of various types of mechanical loading on postnatal cardiomyocytes, we developed a novel "crossbow" bioreactor system capable of independently and dynamically modulating preload and afterload under auxotonic conditions in 3D engineered cardiac tissues. The system employs tunable, curved polydimethylsiloxane (PDMS) cantilever arms that increase resistance to cardiac contractions as they are deflected and a ratcheted center beam to allow for control of preload via change in cardiac tissue length. Culture of cardiobundles made from neonatal rat cardiomyocytes embedded in a fibrin-based hydrogel on the crossbow system reveals physiological, rather than pathological, responses to loading. Progressively increased afterload over two weeks of culture enhances cardiomyocyte contractile force, while progressively increased preload promotes cardiomyocyte elongation and cycling. The crossbow system holds potential for refining our understanding of mechanosensing in cardiac developmental and pathological remodeling, making it a promising tool for

Indexed as

bioreactorheart tissue engineeringmechanobiologyNRVM

Identifiers

PMID41550615
PMCPMC12811015

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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.