Caveolin-1 in cytokine-induced enhancement of intracellular Ca(2+) in human airway smooth muscle.

Sathish V, Abcejo AJ, VanOosten SK, Thompson MA, Prakash YS, Pabelick CM. Caveolin-1 in cytokine-induced enhancement of intracellular Ca2+ in human airway smooth muscle. Am J Physiol Lung Cell Mol Physiol 301: L607-L614, 2011. First published July 29, 2011; doi: 10.1152/ajplung.00019.2011.-Diseases such as asthma are characterized by airway hyperresponsiveness. Enhanced airway smooth muscle (ASM) intracellular Ca2+ ([Ca2+](i)) response to agonist stimulation leading to increased airway constriction has been suggested to contribute to airway hyperresponsiveness. Caveolae are flask-shaped plasma membrane invaginations that express the scaffolding protein caveolin and contain multiple proteins important in [Ca2+](i) signaling (e.g., agonist receptors, ion channels). We recently demonstrated that caveolae and caveolin-1 are important in [Ca2+](i) regulation in human ASM. Proinflammatory cytokines such as tumor necrosis factor (TNF)-alpha and interleukin (IL)-13 modulate [Ca2+](i) in ASM. We hypothesized that cytokine upregulation of caveolar signaling in ASM contributes to enhanced agonist-induced [Ca2+](i) in inflammation. Enzymatically dissociated human ASM cells were exposed to medium (control), 20 ng/ml TNF-alpha, or 50 ng/ml IL-13 for 24 h. Caveolae-enriched membrane fractions displayed substantial increase in caveolin-1 and -2 expressions by TNF-alpha and IL-13. Transfection with caveolin-1-mRed DNA substantially accelerated and increased plasma membrane caveolin-1 expression by TNF-alpha and to a lesser extent by IL-13. Caveolin-1 enhancement was inhibited by nuclear factor-kappa B and mitogen-activated protein kinase inhibitors. In fura 2-loaded ASM cells, [Ca2+](i) responses to 1 mu M ACh, 10 mu M histamine, or 10 nM bradykinin were all exaggerated by TNF-alpha as well as IL-13 exposure. However, disruption of caveolae using caveolin-1 suppression via small-interfering RNA resulted in significant blunting of agonist-induced [Ca2+](i) responses of vehicle and TNF-alpha-exposed cells. These functional data were correlated to the presence of TNFR1 receptor (but not the IL-4/IL-13 receptor) within caveolae. Overall, these results indicate that caveolin-1 plays an important role in airway inflammation by modulating the effect of specific cytokines on [Ca2+](i).