Akkermansia muciniphila exerts immunomodulatory and anti-inflammatory effects on gliadin-stimulated THP-1 derived macrophages

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作者
Sara Molaaghaee-Rouzbahani
Nastaran Asri
Anna Sapone
Kaveh Baghaei
Abbas Yadegar
Davar Amani
Mohammad Rostami-Nejad
机构
[1] Shahid Beheshti University of Medical Sciences,Department of Immunology, School of Medicine
[2] Shahid Beheshti University of Medical Sciences,Gastroenterology and Liver Diseases Research Center, Research Institute for Gastroenterology and Liver Diseases
[3] Massachusetts General Hospital,Center for Celiac Research and Treatment
[4] Shahid Beheshti University of Medical Sciences,Foodborne and Waterborne Diseases Research Center, Research Institute for Gastroenterology and Liver Diseases
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Macrophages (MQs) pro-inflammatory phenotype is triggered by gliadin peptides. Akkermansia muciniphila (A. muciniphila) showed to enhance the anti-inflammatory phenotype of MQs. This study aimed to investigate the anti-inflammatory effects of A. muciniphila, on gliadin stimulated THP-1 derived macrophages. THP-1 cell line monocytes were differentiated into MQs by phorbol 12-myristate 13-acetate (PMA). MQs were treated with A. muciniphila before and after stimulation with gliadin (pre- and post-treat). CD11b, as a marker of macrophage differentiation, and CD206 and CD80, as M1 and M2 markers, were evaluated by flow cytometry technique. The mRNA expression of TGF-β, IL-6, and IL-10 and protein levels of IL-10 and TNF-α were measured by RT-PCR and ELISA techniques, respectively. Results show an increased percentage of M1 phenotype and release of proinflammatory cytokines (like TNF-α and IL-6) by macrophages upon incubation with gliadin. Pre- and post-treatment of gliadin-stimulated macrophages with A. muciniphila induced M2 phenotype associated with decreased proinflammatory (IL-6, TNF-α) and increased anti-inflammatory (IL-10, TGF-β) cytokines expression relative to the group that was treated with gliadin alone. This study suggests the potential beneficial effect of A. muciniphila on gliadin-stimulated MQs and the importance of future studies focusing on their exact mechanism of action on these cells.
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