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Published ahead of print on February 5, 2004, doi:10.1165/rcmb.2003-0313OC
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American Journal of Respiratory Cell and Molecular Biology. Vol. 31, pp. 36-42, 2004
© 2004 American Thoracic Society
DOI: 10.1165/rcmb.2003-0313OC


Original Article

Modulation of Calcium Signaling by Interleukin-13 in Human Airway Smooth Muscle

Role of CD38/Cyclic Adenosine Diphosphate Ribose Pathway

Deepak A. Deshpande, Soner Dogan, Timothy F. Walseth, Steven M. Miller, Yassine Amrani, Reynold A. Panettieri and Mathur S. Kannan

Departments of Veterinary PathoBiology and Pharmacology, University of Minnesota, St. Paul; Department of Physiology, Mayo Clinic, Rochester, Minnesota; and Department of Medicine, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania

Address correspondence to: Mathur S. Kannan, Professor of Pharmacology, Department of Veterinary PathoBiology, College of Veterinary Medicine, 205 Veterinary Science, 1971 Commonwealth Avenue, St. Paul, MN 55108. E-mail: kanna001{at}umn.edu

CD38/cyclic adenosine diphosphate ribose (cADPR) signaling plays an important role in the regulation of intracellular calcium responses to agonists in a variety of cells, including airway smooth muscle (ASM) cells. The present study was aimed at determining the effect of interleukin (IL)-13, a cytokine implicated in the pathogenesis of asthma, on CD38/cADPR signaling and to ascertain the contribution of CD38/cADPR signaling to IL-13–induced airway hyperresponsiveness. Human ASM cells maintained in culture were exposed to 50 ng/ml IL-13 for 22 h and levels of CD38 expression and intracellular calcium responses to agonists were measured. Treatment of human ASM cells with IL-13 resulted in increased CD38 expression as determined by real-time polymerase chain reaction, Western blot analysis, and indirect immunofluorescence. Increased CD38 expression was reflected as increased ADP-ribosyl cyclase activity in the ASM cell membranes. The net intracellular calcium responses to bradykinin, thrombin, and histamine were significantly (P <= 0.05) higher in cells treated with IL-13 compared with controls. Furthermore, 8-bromo-cADPR, a cADPR antagonist, attenuated IL-13–induced augmented intracellular calcium responses to agonists in human ASM cells. These findings indicate that the CD38/cADPR–dependent pathway has a major role in IL-13–induced modulation of calcium signaling in human ASM.

Abbreviations: 8-bromo-cyclic adenosine diphosphate ribose, 8br-cADPR • airway hyperresponsiveness, AHR • airway smooth muscle, ASM • bovine serum albumin, BSA • cyclic adenosine diphosphate ribose, cADPR • number of cycles required to achieve threshold fluorescence, Ct • cyclic guanosine diphosphoribose, cGDPR • human airway smooth muscle, HASM • Hanks' balanced salt solution, HBSS • interleukin, IL • nicotinamide adenine dinucleotide, NAD • reverse transcriptase–polymerase chain reaction, RT-PCR • T helper, Th




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