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Strengths and opportunities in research into extracellular matrix ageing: A consultation with the ECMage research community

Lookup NU author(s): Dr Daryl Shanley

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This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0).


Abstract

© 2024 The Authors. BioEssays published by Wiley Periodicals LLC.Ageing causes progressive decline in metabolic, behavioural, and physiological functions, leading to a reduced health span. The extracellular matrix (ECM) is the three-dimensional network of macromolecules that provides our tissues with structure and biomechanical resilience. Imbalance between damage and repair/regeneration causes the ECM to undergo structural deterioration with age, contributing to age-associated pathology. The ECM ‘Ageing Across the Life Course’ interdisciplinary research network (ECMage) was established to bring together researchers in the United Kingdom, and internationally, working on the emerging field of ECM ageing. Here we report on a consultation at a joint meeting of ECMage and the Medical Research Council / Versus Arthritis Centre for Integrated Research into Musculoskeletal Ageing, held in January 2023, in which delegates analysed the key questions and research opportunities in the field of ECM ageing. We examine fundamental biological questions, enabling technologies, systems of study and emerging in vitro and in silico models, alongside consideration of the broader challenges facing the field.


Publication metadata

Author(s): Dalby MJ, Pekovic-Vaughan V, Shanley DP, Swift J, White LJ, Canty-Laird EG

Publication type: Article

Publication status: Published

Journal: BioEssays

Year: 2024

Pages: epub ahead of print

Online publication date: 24/03/2024

Acceptance date: 07/03/2024

Date deposited: 17/04/2024

ISSN (print): 0265-9247

ISSN (electronic): 1521-1878

Publisher: John Wiley and Sons Inc

URL: https://doi.org/10.1002/bies.202300223

DOI: 10.1002/bies.202300223

Data Access Statement: The data that support the findings of this study are available from the upon reasonable request

PubMed id: 38522027


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Funding

Funder referenceFunder name
BB/W018314/1
MR/P020941/1

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