Expression and activation of the oxytocin receptor in airway smooth muscle cells: Regulation by TNF[alpha] and IL-13

• Published in: Respiratory research 2010-07, Vol.11 (1), p.104
• Main Authors: Amrani, Yassine, Syed, Farhat, Huang, Chris, Li, Katherine, Liu, Veronica, Jain, Deepika, Keslacy, Stefan, Sims, Michael W, Baidouri, Hasna, Cooper, Philip R, Zhao, Hengjiang, Siddiqui, Salman, Brightling, Christopher E, Griswold, Don, Li, Lily, Panettieri, Reynold A., Jr
• Format: Article
• Language: English
• Subjects: Analysis; Asthma; Cell receptors; Enzyme-linked immunosorbent assay; Health aspects; Interleukin-13; Interleukins; Physiological aspects; Pregnancy; Risk factors; Smooth muscle; Tumor necrosis factor
• ISSN: 1465-9921
• DOI: 10.1186/1465-9921-11-104

Background During pregnancy asthma may remain stable, improve or worsen. The factors underlying the deleterious effect of pregnancy on asthma remain unknown. Oxytocin is a neurohypophyseal protein that regulates a number of central and peripheral responses such as uterine contractions and milk ejection. Additional evidence suggests that oxytocin regulates inflammatory processes in other tissues given the ubiquitous expression of the oxytocin receptor. The purpose of this study was to define the role of oxytocin in modulating human airway smooth muscle (HASMCs) function in the presence and absence of IL-13 and TNF[alpha], cytokines known to be important in asthma. Method Expression of oxytocin receptor in cultured HASMCs was performed by real time PCR and flow cytomery assays. Responses to oxytocin was assessed by fluorimetry to detect calcium signals while isolated tracheal rings and precision cut lung slices (PCLS) were used to measure contractile responses. Finally, ELISA was used to compare oxytocin levels in the bronchoalveloar lavage (BAL) samples from healthy subjects and those with asthma. Results PCR analysis demonstrates that OXTR is expressed in HASMCs under basal conditions and that both interleukin (IL)-13 and tumor necrosis factor (TNF[alpha]) stimulate a time-dependent increase in OXTR expression at 6 and 18 hr. Additionally, oxytocin increases cytosolic calcium levels in fura-2-loaded HASMCs that were enhanced in cells treated for 24 hr with IL-13. Interestingly, TNF[alpha] had little effect on oxytocin-induced calcium response despite increasing receptor expression. Using isolated murine tracheal rings and PCLS, oxytocin also promoted force generation and airway narrowing. Further, oxytocin levels are detectable in bronchoalveolar lavage (BAL) fluid derived from healthy subjects as well as from those with asthma. Conclusion Taken together, we show that cytokines modulate the expression of functional oxytocin receptors in HASMCs suggesting a potential role for inflammation-induced changes in oxytocin receptor signaling in the regulation of airway hyper-responsiveness in asthma.