Published ahead of print on February 5, 2004, doi:10.1165/rcmb.2003-0313OC
American Journal of Respiratory Cell and Molecular Biology. Vol. 31, pp. 36-42, 2004
© 2004 American Thoracic Society DOI: 10.1165/rcmb.2003-0313OC
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-13induced 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-13induced augmented intracellular calcium responses to agonists in human ASM cells. These findings indicate that the CD38/cADPRdependent pathway has a major role in IL-13induced 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 transcriptasepolymerase chain reaction, RT-PCR T helper, Th
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Copyright © 2004 American Thoracic Society.
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