Genetic and Pharmacological Dissection of the Role of Spleen Tyrosine Kinase (Syk) in Intestinal Inflammation and Immune Dysfunction in Inflammatory Bowel Diseases. Issue 1 (19th December 2017)

• Record Type: Journal Article
• Authors: Biagioli, Michele; Mencarelli, Andrea; Carino, Adriana; Cipriani, Sabrina; Marchianò, Silvia; Fiorucci, Chiara; Donini, Annibale; Graziosi, Luigina; Baldelli, Franco; Distrutti, Eleonora; Costantino, Gabriele; Fiorucci, Stefano
• Is Part Of: Inflammatory bowel diseases. Volume 24:Issue 1(2018)
• Page Start: 123
• Page End: 135
• Publication Date: 2017-12-19
• Subjects: inflammatory bowel diseases -- DNAX adaptor protein 12 -- spleen tyrosine kinase -- immunity; Inflammatory bowel diseases -- Periodicals; Colitis, Ulcerative -- Periodicals; Crohn Disease -- Periodicals; Inflammatory Bowel Diseases -- Periodicals; 616.344
• DOI: 10.1093/ibd/izx031
• Languages: English
• ISSNs: 1078-0998

Abstract

Abstract: Background: The DNAX adaptor protein 12 (DAP12) is a transmembrane adaptor molecule that signals through the activation of Syk (Spleen Tyrosine Kinase) in myeloid cells. The purpose of this study is to investigate the role of DAP12 and Syk pathways in inflammatory bowel diseases (IBDs). Methods: DAP12 deficient and DAP12 transgenic, overexpressing an increased amount of DAP12, mice and Syk deficient mice in the C57/BL6 background were used for these studies. Colitis was induced by administering mice with dextran sulfate sodium (DSS), in drinking water, or 2, 4, 6-trinitrobenzene sulfonic acid (TNBS), by intrarectal enema. Results: Abundant expression of DAP12 and Syk was detected in colon samples obtained from Crohn's disease patients with expression restricted to immune cells infiltrating the colonic wall. In rodents development of DSS colitis as measured by assessing severity of wasting diseases, global colitis score, and macroscopic and histology scores was robustly attenuated in DAP12 -/- and Syk -/- mice. In contrast, DAP12 overexpression resulted in a striking exacerbation of colon damage caused by DSS. Induction of colon expression of proinflammatory cytokines and chemokines in response to DSS administration was attenuated in DAP12 -/- and Syk -/- mice, whereas opposite results were observed in DAP12 transgenic mice. Treating wild-type mice with a DAP-12 inhibitor or a Syk inhibitor caused a robust attenuation of colitis induced by DSS and TNBS. Conclusions: DAP12 and Syk are essential mediators in inflammation-driven immune dysfunction in murine colitides. Because DAP12 and Syk expression is upregulated in patients with active disease, present findings suggest a beneficial role for DAP12 and Syk inhibitors in IBD.