Evidence map›Paper›PMID 40506498›Full record

ArticleNature materials2025

Hybrid hydrogel-extracellular matrix scaffolds identify biochemical and mechanical signatures of cardiac ageing.

Avery Rui Sun, Md Faris H Ramli, Xingyu Shen, Karthikbabu Kannivadi Ramakanth, Dixiao Chen, Yang Hu, Prasanna Vidyasekar, Roger S Foo, Yuchen Long, Jin Zhu and 2 more

Abstract read
In one paragraph

Article in Nature materials, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing 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

29 citing papers in PubMed.

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  20. Cardio-Vascular Extracellular Matrix: The Unmet Enigma.International journal of molecular sciences · 2026
    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

12 authors.

Avery Rui SunMechanobiology Institute (MBI), National University of Singapore, Singapore, Singapore.ORCID 0000-0002-5991-4435
Md Faris H RamliMechanobiology Institute (MBI), National University of Singapore, Singapore, Singapore.ORCID 0009-0008-9643-2487
Xingyu ShenMechanobiology Institute (MBI), National University of Singapore, Singapore, Singapore.ORCID 0009-0002-5961-7884
Karthikbabu Kannivadi RamakanthDepartment of Biological Sciences, National University of Singapore, Singapore, Singapore.ORCID 0000-0002-5598-9763
Dixiao ChenMechanobiology Institute (MBI), National University of Singapore, Singapore, Singapore.ORCID 0009-0004-0402-2183
Yang HuCardiovascular-Metabolic Disease Translational Research Programme, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Prasanna VidyasekarCardiovascular-Metabolic Disease Translational Research Programme, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Roger S FooCardiovascular-Metabolic Disease Translational Research Programme, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.ORCID 0000-0002-8079-4618
Yuchen LongMechanobiology Institute (MBI), National University of Singapore, Singapore, Singapore.ORCID 0000-0001-5071-4632
Jin ZhuMechanobiology Institute (MBI), National University of Singapore, Singapore, Singapore.
Matthew Ackers-JohnsonCardiovascular-Metabolic Disease Translational Research Programme, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.ORCID 0000-0002-1308-6785
Jennifer L YoungMechanobiology Institute (MBI), National University of Singapore, Singapore, Singapore. biejly@nus.edu.sg.ORCID 0000-0002-5229-5168

Funding

Ministry of Education - Singapore (MOE) MOET32021-0003
6 · The paper itself

Abstract

Extracellular matrix remodelling of cardiac tissue is a key contributor to age-related cardiovascular disease and dysfunction. Such remodelling is multifaceted including changes to the biochemical composition, architecture and mechanics, clouding our understanding of how and which extracellular matrix properties contribute to a dysfunctional state. Here we describe a decellularized extracellular matrix-synthetic hydrogel hybrid scaffold that independently confers two distinct matrix properties-ligand presentation and stiffness-to cultured cells in vitro, allowing for the identification of their specific roles in cardiac ageing. The hybrid scaffold maintains native matrix composition and organization of young or aged murine cardiac tissue, whereas its mechanical properties can be independently tuned to mimic young or aged tissue stiffness. Seeding these scaffolds with murine primary cardiac fibroblasts, we identify distinct age- and matrix-dependent mechanisms of cardiac fibroblast activation, matrix remodelling and senescence. Importantly, we show that the ligand presentation of a young extracellular matrix can outweigh the profibrotic stiffness cues typically present in an aged extracellular matrix in maintaining or driving cardiac fibroblast quiescence. Ultimately, these tunable scaffolds can enable the discovery of specific extracellular targets to prevent ageing dysfunction and promote rejuvenation.

Indexed as

AgingExtracellular MatrixHeartHydrogelsMyocardiumTissue ScaffoldsAnimalsCells, CulturedFibroblastsMiceMice, Inbred C57BLHydrogels

Identifiers

PMID40506498
PMCPMC12404999

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LicenceCC BY-NC-ND
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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.