Promoting effects of IL-13 on Ca2+ release and store-operated Ca2+ entry in airway smooth muscle cells

被引:44
|
作者
Gao, Ya-dong [1 ]
Zou, Jin-jing [1 ]
Zheng, Jun-wen [1 ]
Shang, Min [1 ]
Chen, Xia [1 ]
Geng, Shuang [1 ]
Yang, Jiong [1 ]
机构
[1] Wuhan Univ, Dept Resp Med, Zhongnan Hosp, Wuhan 430071, Peoples R China
基金
中国博士后科学基金;
关键词
Airway smooth muscle; IL-13; Ca2+ channels; Store-operated; Glucocorticoids; beta(2) adrenoceptor; Proliferation; CALCIUM-CHANNEL; CD38; EXPRESSION; ALLERGIC-ASTHMA; INTERLEUKIN-13; PROLIFERATION; GLUCOCORTICOIDS; DEXAMETHASONE; INFLUX; INHIBITION; CYTOKINES;
D O I
10.1016/j.pupt.2009.12.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Th2 cytokine interleukin (IL)-13 plays a central role in the pathogenesis of allergic asthma. IL-13 exhibits a direct effect on airway smooth muscle cells (ASMCs) to cause airway hyperresponsiveness. IL-13 has been demonstrated to regulate Ca2+ signaling in ASMCs, but the underlying mechanisms are not fully understood. Store-operated Ca2+ entry (SOCE) plays an important role in regulating Ca2+ signaling and cellular responses of ASMCs, whether IL-13 affects SOCE in ASMCs has not been reported. In this study, by using confocal Ca2+ fluorescence imaging, we found that IL-13 (10 ng/ml) treatment increased basal intracellular Ca2+ ([Ca2+]1) level, Ca2+ release and SOCE induced by SERCA inhibitor thapsigargin in rat bronchial smooth muscle cells. The glucocorticoid dexamethasone and the short-acting beta 2 adrenergic agonist (beta 2 agonist) salbutamol suppressed IL-13-augumented basal [Ca2+](i), Ca2+ release and SOCE, whereas the long-acting 32 agonist salmeterol had no effect on altered Ca2+ signaling in IL-13-treated ASMCs. Membrane-permeable cAMP analog dibutyryl-cAMP (db-cAMP) similarly decreased Ca2+ release and SOCE induced by thapsigargin in IL-13-treated ASMCs, confirmed a role of cAMP/PKA signaling pathway in the regulation of SOCE. IL-13 promoted the proliferation of ASMCs stimulated by serum; this effect was inhibited by nonspecific Ca2+ channel blockers SKF-96365 and NiCl2, by salmeterol, but not by salbutamol and dexamethasone. IL-13 treatment did not change the expression of SOC channel-associated molecules STIM1, Orai1 and TRPC1 at mRNA level. Our findings identified a promoting effect of IL-13 on Ca2+ release and SOCE in ASMCs, which partially contributes to its effect on the proliferation of ASMCs; the differences of glucocorticoids and beta 2 agonists in inhibiting Ca2+ signal and proliferation potentiated by IL-13 suggest that these therapies of asthma may have distinct effect on the relief of airway contraction and remodeling in bronchial asthma. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:182 / 189
页数:8
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