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Salmonella-driven intestinal edema in mice is characterized by tensed fibronectin fibers

Abstract:
Intestinal edema is a common manifestation of numerous gastrointestinal diseases and is characterized by the accumulation of fluid in the interstitial space of the intestinal wall. Technical advances in laser capture microdissection and low-biomass proteomics now allow us to specifically characterize the intestinal edema proteome. Using advanced proteomics, we identify peptides derived from antimicrobial factors with high signal intensity, but also highlight major contributions from the blood clotting system, extracellular matrix (ECM) and protease–protease inhibitor networks. The ECM is a complex fibrillar network of macromolecules that provides structural and mechanical support to the intestinal tissue. One abundant component of the ECM observed in Salmonella-driven intestinal edema is the glycoprotein fibronectin, recognized for its structure–function interplay regulated by mechanical forces. Using mechanosensitive staining of fibronectin fibers reveals that they are tensed in the edema, despite the high abundance of proteases able to cleave fibronectin. In contrast, fibronectin fibers increasingly relax in other cecal tissue areas as the infection progresses. Co-staining for fibrin(ogen) indicates the formation of a provisional matrix in the edema, similar to what is observed in response to skin injury, while collagen staining reveals a sparse and disrupted collagen fiber network. These observations plus the absence of low tensional fibronectin fibers and the additional finding of a high number of protease inhibitors in the edema proteome could indicate a critical role of stretched fibronectin fibers in maintaining tissue integrity in the severely inflamed cecum. Understanding these processes may also provide valuable functional diagnostic markers of intestinal disease progression in the future.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1111/febs.17120

Authors

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Role:
Author
ORCID:
0000-0001-5698-1977
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Role:
Author
ORCID:
0000-0003-3907-9281
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Role:
Author
ORCID:
0000-0002-3431-7415
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Role:
Author
ORCID:
0000-0003-2898-7671
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Institution:
University of Oxford
Division:
MSD
Department:
Pathology Dunn School
Oxford college:
Queen's College
Role:
Author
ORCID:
0000-0002-2473-1145


Publisher:
Wiley
Journal:
FEBS Journal More from this journal
Volume:
291
Issue:
14
Pages:
3104-3127
Publication date:
2024-03-15
Acceptance date:
2025-03-05
DOI:
EISSN:
1742-4658
ISSN:
1742-464X
Pmid:
38487972


Language:
English
Keywords:
Pubs id:
2120843
Local pid:
pubs:2120843
Deposit date:
2025-04-30
ARK identifier:

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