Journal Article

Calcium-Sensing Receptor as a Novel Target for the Treatment of Idiopathic Pulmonary Fibrosis

Huang, Ping, Jurkowska, Renata Z., Simpson, A. John, Hope-Gill, Benjamin D., de Araújo, Rachel Paes, Haddadi, Bahareh Sadat, Riccardi, Daniela, Ward, Jeremy P. T., Karmouty-Quintana, Harry, Mansfield, Bethan, Li, Renjiao, Pass, Daniel A., Ecker, Rupert, Lewis, Keir E., Bruce, Richard T., Dally, Jordanna, Corrigan, Christopher J., Moseley, Ryan, Mur, Luis A. J., Yarova, Polina L., Wolffs, Kasope

2025

Overview

Idiopathic pulmonary fibrosis (IPF) is a disease with a poor prognosis and no curative therapies. Fibroblast activation by transforming growth factor β1 (TGFβ1) and disrupted metabolic pathways, including the arginine–polyamine pathway, play crucial roles in IPF development. Polyamines are agonists of the calcium/cation-sensing receptor (CaSR), activation of which is detrimental for asthma and pulmonary hypertension, but its role in IPF is unknown. To address this question, we evaluated polyamine abundance using metabolomic analysis of IPF patient saliva. Furthermore, we examined CaSR functional expression in human lung fibroblasts (HLFs), assessed the anti-fibrotic effects of a CaSR antagonist, NPS2143, in TGFβ1-activated normal and IPF HLFs by RNA sequencing and immunofluorescence imaging, respectively; and NPS2143 effects on polyamine synthesis in HLFs by immunoassays. Our results demonstrate that polyamine metabolites are increased in IPF patient saliva. Polyamines activate fibroblast CaSR in vitro, elevating intracellular calcium concentration. CaSR inhibition reduced TGFβ1-induced polyamine and pro-fibrotic factor expression in normal and IPF HLFs. TGFβ1 directly stimulated polyamine release by HLFs, an effect that was blocked by NPS2143. This suggests that TGFβ1 promotes CaSR activation through increased polyamine expression, driving a pro-fibrotic response. By halting some polyamine-induced pro-fibrotic changes, CaSR antagonists exhibit disease-modifying potential in IPF onset and development.

• Publisher: MDPI AG,MDPI
• Subject: Amino acids / Arginine / arginine–polyamine pathway / Asthma / Benzamides / Calcium (intracellular) / Calcium-sensing receptors / calcium/cation-sensing receptor / Chronic obstructive pulmonary disease / Cyclohexylamines / Enzymes / Female / Fibroblasts / Fibroblasts - drug effects / Fibroblasts - metabolism / Fibrosis / Growth factors / Humans / Hypertension / idiopathic pulmonary fibrosis / Idiopathic Pulmonary Fibrosis - drug therapy / Idiopathic Pulmonary Fibrosis - metabolism / Idiopathic Pulmonary Fibrosis - pathology / Immunofluorescence / Kinases / Lung - metabolism / Lung - pathology / Lung diseases / Lung transplants / Male / Metabolic pathways / Metabolism / Metabolites / Metabolomics / Microscopy / Monoclonal antibodies / Naphthalenes - pharmacology / negative allosteric modulator / Pathogenesis / Pollutants / Polyamines / Polyamines - metabolism / Prognosis / Proteins / Pulmonary fibrosis / Pulmonary hypertension / Receptors, Calcium-Sensing - antagonists & inhibitors / Receptors, Calcium-Sensing - genetics / Receptors, Calcium-Sensing - metabolism / RNA / RNA sequencing / Saliva / TGFβ1 / Transforming Growth Factor beta1 - metabolism / Transforming Growth Factor beta1 - pharmacology / Transforming growth factor-b1 / Transforming growth factors