P2Y2 receptor antagonism resolves sialadenitis and improves salivary flow in a Sjögren’s syndrome mouse model

• Published in: Archives of oral biology 2021-04, Vol.124, p.105067-105067, Article 105067
• Main Authors: Jasmer, Kimberly J., Woods, Lucas T., Forti, Kevin Muñoz, Martin, Adam L., Camden, Jean M., Colonna, Marco, Weisman, Gary A.
• Format: Article
• Language: English
• Subjects: Alarmins; Autoimmune disease; B lymphocytes; Nucleotide; Purinergic receptor; Sjögren’s syndrome
• ISSN: 0003-9969; 1879-1506
• DOI: 10.1016/j.archoralbio.2021.105067

•Systemic or localized delivery of the selective P2Y2R antagonist, AR-C118925, were evaluated in the NOD.H-2h4,IFNγ−/−,CD28−/− SS mouse model.•Systemic administration of AR-C118925 resolves salivary gland inflammation and improves saliva flow in NOD.H-2h4,IFNγ−/−,CD28−/− mice.•Single-dose localized administration of AR-C118925 did not resolve inflammation or affect saliva flow in NOD.H-2h4,IFNγ−/−,CD28−/− mice.•Functional P2Y2Rs are expressed in isolated salivary gland B lymphocytes.•P2Y2Rs expressed in salivary gland B lymphocytes promote migration and IgM secretion. Sjögren’s syndrome (SS) is a chronic autoimmune exocrinopathy characterized by lymphocytic infiltration of the salivary and lacrimal glands and decreased saliva and tear production. Previous studies indicate that the G protein-coupled P2Y2 nucleotide receptor (P2Y2R) is upregulated in numerous models of salivary gland inflammation (i.e., sialadenitis), where it has been implicated as a key mediator of chronic inflammation. Here, we evaluate both systemic and localized P2Y2R antagonism as a means to resolve sialadenitis in the NOD.H-2h4,IFNγ−/−,CD28−/− (NOD.H-2h4 DKO) mouse model of SS. Female 4.5 month old NOD.H-2h4 DKO mice received daily intraperitoneal injections for 10 days of the selective P2Y2R antagonist, AR-C118925, or vehicle-only control. Single-dose localized intraglandular antagonist delivery into the Wharton’s duct was also evaluated. Carbachol-induced saliva was measured and then submandibular glands (SMGs) were isolated and either fixed and paraffin-embedded for H&E staining, homogenized for RNA isolation or dissociated for flow cytometry analysis. Intraperitoneal injection, but not localized intraglandular administration, of AR-C118925 significantly enhanced carbachol-induced salivation and reduced lymphocytic foci and immune cell markers in SMGs of 5 month old NOD.H-2h4 DKO mice, compared to vehicle-injected control mice. We found that B cells represent the primary immune cell population in inflamed SMGs of NOD.H-2h4 DKO mice that express elevated levels of P2Y2R compared to C57BL/6 control mice. We further demonstrate a role for P2Y2Rs in mediating B cell migration and the release of IgM. Our findings suggest that the P2Y2R represents a novel therapeutic target for the treatment of Sjögren’s syndrome.