Evidence map›Paper›PMID 42733195›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

Unravelling the Distinct Phenotype and Mechanosensitive Properties of Different Tendon Cell Populations.

S E Grossemy, D E Zamboulis, N S Khatib, M R Fazal, C C Gains, A Giannopoulos, T Hopkins, C Bevan, Y Aggarwal, M M Knight and 1 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

11 authors.

S E GrossemyCentre for Predictive In Vitro Models, Queen Mary University of London, London, UK.ORCID https://orcid.org/0009-0001-1491-268X
D E ZamboulisCentre for Predictive In Vitro Models, Queen Mary University of London, London, UK.ORCID https://orcid.org/0000-0003-2839-7620
N S KhatibCentre for Predictive In Vitro Models, Queen Mary University of London, London, UK.
M R FazalCentre for Predictive In Vitro Models, Queen Mary University of London, London, UK.
C C GainsCentre for Predictive In Vitro Models, Queen Mary University of London, London, UK.
A GiannopoulosCentre for Predictive In Vitro Models, Queen Mary University of London, London, UK.
T HopkinsCentre for Predictive In Vitro Models, Queen Mary University of London, London, UK.ORCID https://orcid.org/0000-0002-0300-8230
C BevanCentre for Predictive In Vitro Models, Queen Mary University of London, London, UK.ORCID https://orcid.org/0009-0005-5102-8542
Y AggarwalCentre for Predictive In Vitro Models, Queen Mary University of London, London, UK.
M M KnightCentre for Predictive In Vitro Models, Queen Mary University of London, London, UK.ORCID https://orcid.org/0000-0003-3755-1597
H R C ScreenCentre for Predictive In Vitro Models, Queen Mary University of London, London, UK.ORCID https://orcid.org/0000-0002-9077-0732

Funding

Dunhill Medical Charity RPGF1802∖23UK RMP - MRC MR/T015462/1
6 · The paper itself

Abstract

Tendinopathy arises from maladaptive cellular responses, though the drivers remain unclear. Here we isolate and characterise an overlooked tendon cell population residing within interfascicular matrix (IFM), demonstrating its importance as a highly mechanosensitive cell in tendon. We describe the first successful isolation and long-term culture of enriched populations of primary IFM and fascicular matrix (FM) cells, enabling direct comparison of their phenotypes and mechanosensitivity. IFM cells exhibited a potent response to stiff substrates, displaying cytoskeletal remodelling, rapid drifting of tenogenic and ECM gene expression, and proliferative decline, while FM cells remained largely unaltered. Crucially, transferring IFM cells to compliant, IFM-like substrates recovered their proliferative capacity, morphology, and partially restored their gene expression. This work defines IFM cells as a highly mechanosensitive tendon cell population. Importantly, it also enables the establishment of a defined culture framework that supports the maintenance of key IFM phenotypic characteristics in vitro and provides a new perspective on tendon cell heterogeneity by identifying distinct compartment-specific responses to the mechanical microenvironment.

Indexed as

ECMfascicular matrix (FM)interfascicular matrix (IFM)mechanoresponsephenotypic driftstiffnesstendon cell populationstenocytes

Identifiers

PMID42733195
PMCPMC13572792

What OpenQuestion holds

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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.