The calcium-sensing receptor modulates the prostaglandin E2 pathway in intestinal inflammation

• Published in: Frontiers in pharmacology Vol. 14; p. 1151144
• Main Authors: Gushchina, Valeriya, Kupper, Nadja, Schwarzkopf, Michael, Frisch, Gitta, Piatek, Karina, Aigner, Cornelia, Michel, Alexandra, Schueffl, Hemma, Iamartino, Luca, Elajnaf, Taha, Manhardt, Teresa, Vlasaty, Andrea, Heffeter, Petra, Bassetto, Marcella, Kállay, Enikö, Schepelmann, Martin
• Format: Journal Article
• Language: English
• Published: Frontiers Media S.A 20.04.2023
• Subjects: calcilytic; calcimimetic; calcium-sensing receptor (CaSR); colitis; inflammation; Pharmacology; prostaglandins
• ISSN: 1663-9812; 1663-9812
• DOI: 10.3389/fphar.2023.1151144

Introduction: The prostaglandin E 2 (PGE 2 ) pathway is one of the main mediators of intestinal inflammation. As activation of the calcium-sensing receptor (CaSR) induces expression of inflammatory markers in the colon, we assessed the impact of the CaSR on the PGE 2 pathway regulation in colon cancer cells and the colon in vitro and in vivo . Methods and Results: We treated CaSR-transfected HT29 and Caco-2 colon cancer cell lines with different orthosteric ligands or modulators of the CaSR and measured gene expression and PGE 2 levels. In CaSR-transfected HT29 CaSR-GFP and Caco-2 CaSR-GFP cells, the orthosteric CaSR ligand spermine and the positive allosteric CaSR modulator NPS R -568 both induced an inflammatory state as measured by IL-8 gene expression and significantly increased the expression of the PGE 2 pathway key enzymes cyclooxygenase (COX)-2 and/or prostaglandin E 2 synthase 1 (PGES-1). Inhibition of the CaSR with the calcilytic NPS 2143 abolished the spermine- and NPS R -568-induced pro-inflammatory response. Interestingly, we observed cell-line specific responses as e.g . PGES-1 expression was affected only in HT29 CaSR-GFP but not in Caco-2 CaSR-GFP cells. Other genes involved in the PGE 2 pathway (COX-1, or the PGE 2 receptors) were not responsive to the treatment. None of the studied genes were affected by any CaSR agonist in GFP-only transfected HT29 GFP and Caco-2 GFP cells, indicating that the observed gene-inducing effects of spermine and R -568 were indeed mediated by the CaSR. In vivo , we had previously determined that treatment with the clinically approved calcimimetic cinacalcet worsened symptoms in a dextran sulfate sodium (DSS)-induced colitis mouse model. In the colons of these mice, cinacalcet significantly induced gene expression of PGES-2 and the EP3 receptor, but not COX-2; while NPS 2143 increased the expression of the PGE 2 -degrading enzyme 15-hydroxyprostaglandin dehydrogenase (15-PGDH). Importantly, neither treatment had any effect on the colons of non-DSS treated mice. Discussion: Overall, we show that activation of the CaSR induces the PGE 2 pathway, albeit with differing effects in vitro and in vivo . This may be due to the different microenvironment in vivo compared to in vitro , specifically the presence of a CaSR-responsive immune system. Since calcilytics inhibit ligand-mediated CaSR signaling, they may be considered for novel therapies against inflammatory bowel disease.