Evidence map›Paper›PMID 42364739›Full record

ArticleMatrix biology : journal of the International Society for Matrix Biology2026

Airway macrophage specific glycocalyx expression and remodeling following viral infection.

Ziyun Zhang, Iashia Z Nabi, Samie Dalgarno, H Davies-Strickleton, Ilayda Akbulut, Tracy Hussell, Douglas P Dyer

Abstract read
In one paragraph

Article in Matrix biology : journal of the International Society for Matrix Biology, 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

7 authors.

Ziyun ZhangLydia Becker Institute of Immunology and Inflammation, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, University of Manchester, United Kingdom.
Iashia Z NabiLydia Becker Institute of Immunology and Inflammation, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, University of Manchester, United Kingdom; Manchester Cell-Matrix Centre, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, University of Manchester, United Kingdom.
Samie DalgarnoLydia Becker Institute of Immunology and Inflammation, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, University of Manchester, United Kingdom; Manchester Cell-Matrix Centre, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, University of Manchester, United Kingdom.
H Davies-StrickletonManchester Cell-Matrix Centre, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, University of Manchester, United Kingdom.
Ilayda AkbulutLydia Becker Institute of Immunology and Inflammation, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, University of Manchester, United Kingdom.
Tracy HussellLydia Becker Institute of Immunology and Inflammation, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, University of Manchester, United Kingdom. Electronic address: tracy.hussell@manchester.ac.uk.
Douglas P DyerLydia Becker Institute of Immunology and Inflammation, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, University of Manchester, United Kingdom; Manchester Cell-Matrix Centre, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, University of Manchester, United Kingdom; Geoffrey Jefferson Brain Research Centre, Manchester Academic Health Science Centre, Northern Care Alliance NHS Group, University of Manchester, Manchester, United Kingdom. Electronic address: Douglas.dyer@manchester.ac.uk.

Funding

Wellcome Trust
6 · The paper itself

Abstract

The cell surface glycocalyx is a pericellular matrix that surrounds all cells, including macrophages, and regulates their function and interaction with the environment. The glycocalyx is composed of a range of glycans and glyco-proteins and its shedding into the blood is observed in, and is used as a marker of, a variety of inflammatory conditions such as viral infections. However, little is known about the signals and locations that regulate glycocalyx formation and heterogeneity across macrophage subsets. We now report that mouse lung macrophages express a glycocalyx that is dependent on their anatomical location and the mediators driving their differentiation from monocytes. Furthermore, during inflammatory conditions, caused by viral infection, the macrophage glycocalyx is remodelled in complex ways. Overall, our study provides a novel pathway involved in macrophage glycocalyx formation at rest and during inflammatory responses at mucosal tissue sties. This impacts our emerging understanding of the glycocalyx on immune cells beyond the classical paradigm of glycocalyx regulation of endothelial and vascular function.

Indexed as

GlycocalyxMacrophagesMacrophages, AlveolarVirus DiseasesAnimalsCell DifferentiationHumansLungMiceMonocytesGlycocalyxInfectionMacrophageVirus

Identifiers

PMID42364739
PMCPMC7619357

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 Socratic graph.