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Immler, R.* ; Nussbaumer, K.* ; Doerner, A.* ; El Bounkari, O.* ; Huber, S.* ; Abisch, J.* ; Napoli, M.* ; Schmidt, S.* ; Margraf, A.* ; Pruenster, M.* ; Rohwedder, I.* ; Lange-Sperandio, B.* ; Mall, M.A.* ; de Jong, R.J. ; Ohnmacht, C. ; Bernhagen, J.* ; Voehringer, D.* ; Marth, J.D.* ; Frommhold, D.* ; Sperandio, M.*

CCR3-dependent eosinophil recruitment is regulated by sialyltransferase ST3Gal-IV.

Proc. Natl. Acad. Sci. U.S.A. 121:e2319057121 (2024)
Verlagsversion DOI PMC
Open Access Hybrid
Creative Commons Lizenzvertrag
Eosinophil recruitment is a pathological hallmark of many allergic and helminthic diseases. Here, we investigated chemokine receptor CCR3-induced eosinophil recruitment in sialyltransferase St3gal4-/- mice. We found a marked decrease in eosinophil extravasation into CCL11-stimulated cremaster muscles and into the inflamed peritoneal cavity of St3gal4-/- mice. Ex vivo flow chamber assays uncovered reduced adhesion of St3gal4-/- compared to wild type eosinophils. Using flow cytometry, we show reduced binding of CCL11 to St3gal4-/- eosinophils. Further, we noted reduced binding of CCL11 to its chemokine receptor CCR3 isolated from St3gal4-/- eosinophils. This was accompanied by almost absent CCR3 internalization of CCL11-stimulated St3gal4-/- eosinophils. Applying an ovalbumin-induced allergic airway disease model, we found a dramatic reduction in eosinophil numbers in bronchoalveolar lavage fluid following intratracheal challenge with ovalbumin in St3gal4-deficient mice. Finally, we also investigated tissue-resident eosinophils under homeostatic conditions and found reduced resident eosinophil numbers in the thymus and adipose tissue in the absence of ST3Gal-IV. Taken together, our results demonstrate an important role of ST3Gal-IV in CCR3-induced eosinophil recruitment in vivo rendering this enzyme an attractive target in reducing unwanted eosinophil infiltration in various disorders including allergic diseases.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Asthma ; Chemokines ; Eosinophil ; Inflammation ; Sialylation; P-selectin; Siglec-f; Leukocyte Recruitment; Endothelial-cells; Inflammation; Eotaxin; Trafficking; Roles; Vivo; Accumulation
Sprache englisch
Veröffentlichungsjahr 2024
HGF-Berichtsjahr 2024
ISSN (print) / ISBN 0027-8424
e-ISSN 1091-6490
Zeitschrift Proceedings of the National Academy of Sciences of the United States of America
Quellenangaben Band: 121, Heft: 19, Seiten: , Artikelnummer: e2319057121 Supplement: ,
Verlag National Academy of Sciences
Verlagsort 2101 Constitution Ave Nw, Washington, Dc 20418 Usa
Begutachtungsstatus Peer reviewed
Institut(e) Institute for Allergy Research (IAF)
POF Topic(s) 30202 - Environmental Health
Forschungsfeld(er) Allergy
PSP-Element(e) G-505491-001
G-505400-001
Förderungen NIH HHS
Wellcome Trust
DOI 10.1073/pnas.2319057121
WOS ID 001250555300005
Scopus ID 85191924003
PubMed ID 38687790
Erfassungsdatum 2024-05-22
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