Potent CCR3 receptor antagonist, SB328437, suppresses colonic eosinophil chemotaxis and inflammation in the Winnie Murine Model of spontaneous chronic colitis

Filippone, Rhiannon, Dargahi, Narges ORCID: 0000-0001-8090-025X, Eri, Rajaraman ORCID: 0000-0003-1688-8043, Uranga, Jose A ORCID: 0000-0003-4656-8569, Bornstein, Joel C ORCID: 0000-0002-7518-7717, Apostolopoulos, Vasso ORCID: 0000-0001-6788-2771 and Nurgali, Kulmira ORCID: 0000-0002-2597-6929 (2022) Potent CCR3 receptor antagonist, SB328437, suppresses colonic eosinophil chemotaxis and inflammation in the Winnie Murine Model of spontaneous chronic colitis. International Journal of Molecular Sciences, 23 (14). ISSN 1661-6596

Abstract

Eosinophils and their regulatory molecules have been associated with chronic intestinal inflammation and gastrointestinal dysfunctions; eosinophil accumulation in the gut is prominent in inflammatory bowel disease (IBD). The chemokine receptor CCR3 plays a pivotal role in local and systemic recruitment and activation of eosinophils. In this study, we targeted CCR3-ligand interactions with a potent CCR3 receptor antagonist, SB328437, to alleviate eosinophil-associated immunological responses in the Winnie model of spontaneous chronic colitis. Winnie and C57BL/6 mice were treated with SB328437 or vehicle. Clinical and histopathological parameters of chronic colitis were assessed. Flow cytometry was performed to discern changes in colonic, splenic, circulatory, and bone marrow-derived leukocytes. Changes to the serum levels of eosinophil-associated chemokines and cytokines were measured using BioPlex. Inhibition of CCR3 receptors with SB328437 attenuated disease activity and gross morphological damage to the inflamed intestines and reduced eosinophils and their regulatory molecules in the inflamed colon and circulation. SB328437 had no effect on eosinophils and their progenitor cells in the spleen and bone marrow. This study demonstrates that targeting eosinophils via the CCR3 axis has anti-inflammatory effects in the inflamed intestine, and also contributes to understanding the role of eosinophils as potential end-point targets for IBD treatment.

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Item type Article
URI https://vuir.vu.edu.au/id/eprint/46557
DOI 10.3390/ijms23147780
Official URL https://www.mdpi.com/1422-0067/23/14/7780
Subjects Current > FOR (2020) Classification > 3404 Medicinal and biomolecular chemistry
Current > Division/Research > Institute for Health and Sport
Keywords chronic intestinal inflammation, spontaneous chronic colitis, Winnie model, laboratory mice
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