Evidence map›Paper›PMID 42477090›Full record

ArticleMolecular systems biology2026

Extracellular matrix phenotyping by imaging mass cytometry defines distinct cellular matrix environments associated with allergic airway inflammation.

James E Parkinson, Morgan Bryant, Mohamed Ghafoor, Rebecca J Dodd, Hannah E Tompkins, Martin Fergie, Matthew O Burgess, Magnus Rattray, Tara E Sutherland

Abstract read
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In one paragraph

Article in Molecular systems biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

9 authors.

James E ParkinsonLydia Becker Institute of Immunology and Inflammation, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, M139PT, UK.ORCID http://orcid.org/0000-0003-4881-5121
Morgan BryantInstitute of Medical Sciences, School of Medicine, Medical Sciences and Nutrition, University of Aberdeen, Aberdeen, AB252ZD, UK.ORCID http://orcid.org/0009-0005-3261-0940
Mohamed GhafoorLydia Becker Institute of Immunology and Inflammation, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, M139PT, UK.ORCID http://orcid.org/0000-0002-7757-3224
Rebecca J DoddLydia Becker Institute of Immunology and Inflammation, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, M139PT, UK.ORCID http://orcid.org/0000-0002-4733-138X
Hannah E TompkinsLydia Becker Institute of Immunology and Inflammation, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, M139PT, UK.ORCID http://orcid.org/0000-0001-8361-3627
Martin FergieDivision of Informatics, Imaging & Data Sciences, Faculty of Biology Medicine and Health, University of Manchester, Manchester, M139PT, UK.
Matthew O BurgessInstitute of Medical Sciences, School of Medicine, Medical Sciences and Nutrition, University of Aberdeen, Aberdeen, AB252ZD, UK.ORCID http://orcid.org/0000-0001-9666-6787
Magnus RattrayDivision of Informatics, Imaging & Data Sciences, Faculty of Biology Medicine and Health, University of Manchester, Manchester, M139PT, UK.ORCID http://orcid.org/0000-0001-8196-5565
Tara E SutherlandInstitute of Medical Sciences, School of Medicine, Medical Sciences and Nutrition, University of Aberdeen, Aberdeen, AB252ZD, UK. tara.sutherland@abdn.ac.uk.ORCID http://orcid.org/0000-0001-9334-8206

Funding

Asthma and Lung UK (Asthma UK) MRFAUK-2015-302Medical Research Foundation (MRF) MRFAUK-2015-302UKRI | Medical Research Council (MRC) MR/V011235/1UKRI | Medical Research Council (MRC) MRY0036831Wellcome Trust (WT) 203128/Z/16/ZWellcome Trust (WT) 218491/Z/19/ZWellcome Trust (WT) 220926/Z/20/ZWellcome Trust (WT) 304200/Z/23/Z
6 · The paper itself

Abstract

The extracellular matrix (ECM) forms the scaffold in which cells reside and interact. The composition of this scaffold guides the development of local immune responses and tissue function. With the advent of multiplexed spatial imaging methodologies, investigating the intricacies of cellular spatial organisation is more accessible than ever. However, the relationship between cellular organisation and ECM composition has been broadly overlooked. Using imaging mass cytometry, we investigated the association between cellular niches and their surrounding matrix environment during allergic airway inflammation in two commonly used in-bred mouse strains. We have integrated both intracellular and extracellular analysis by first classifying cells according to their canonical marker expression and then utilising a novel pipeline to independently characterise their ECM environment. Applying this methodology across three distinct lung tissue regions we reveal region-specific and spatially constrained allergic inflammatory responses. In our model of allergic airway inflammation, recruited neutrophils were dispersed within the alveolar parenchyma, alongside a loss of alveolar type-I cells and an expansion of alveolar type-II cells. This activated parenchyma was associated with increased proximity to hyaluronan and chondroitin sulphate. In contrast, infiltrating CD11b

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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.