| Abstract | In human articular joints, synovial fibroblasts (HSFs) have essential physiological functions that include synthesis and secretion of components of the extracellular matrix and essential articular joint lubricants, as well as release of paracrine substances such as ATP. Although the molecular and cellular processes that lead to a rheumatoid arthritis (RA) phenotype are not fully understood, HSF cells exhibit significant changes during this disease progression. The effects of ATP on HSFs were studied by monitoring changes in intracellular Ca2+ ([Ca2+]i), and measuring electrophysiological properties. ATP application to HSF cell populations that had been enzymatically released from 2‐D cell culture revealed that ATP (10–100 μm), or its analogues UTP or ADP, consistently produced a large transient increase in [Ca2+]i. These changes (i) were initiated by activation of the P2Y purinergic receptor family, (ii) required Gq‐mediated signal transduction, (iii) did not involve a transmembrane Ca2+ influx, but instead (iv) arose almost entirely from activation of endoplasmic reticulum (ER)‐localized inositol 1,4,5‐trisphosphate (IP3) receptors that triggered Ca2+ release from the ER. Corresponding single cell electrophysiological studies revealed that these ATP effects (i) were insensitive to [Ca2+]o removal, (ii) involved an IP3‐mediated intracellular Ca2+ release process, and (iii) strongly turned on Ca2+‐activated K+ current(s) that significantly hyperpolarized these cells. Application of histamine produced very similar effects in these HSF cells. Since ATP is a known paracrine agonist and histamine is released early in the inflammatory response, these findings may contribute to identification of early steps/defects in the initiation and progression of RA. |
|---|
