Glycogen synthase kinase-3 regulates cigarette smoke extract- and IL-1beta-induced cytokine secretion by airway smooth muscle.

摘要

Glycogen synthase kinase-3 (GSK-3) is a constitutively active kinase that regulates multiple signaling proteins and transcription factors involved in inflammation. Its role in inflammatory lung diseases, including chronic obstructive pulmonary disease (COPD), is largely unknown. We investigated the role of GSK-3 in the secretion of chemokines and growth factors by human airway smooth muscle cells after exposure to cigarette smoke extract (CSE) or interleukin-1beta (IL-1beta), important factors involved in the development of COPD. Cultured human airway smooth muscle cells were exposed to increasing concentrations of CSE (1-15%) and IL-1beta (0.01-1.0 ng/ml), which induced the secretion of VEGF-A and IL-8, whereas eotaxin secretion was induced by IL-1beta only. Inhibition of GSK-3 by the selective inhibitor SB216763 or CHIR/CT99021 attenuated the cytokine and growth factor release induced by CSE and/or IL-1beta, without affecting the basal release. Secretion of the cytokines by airway smooth muscle partially depends on NF-kappaB signaling, and GSK-3 has been implicated in regulating multiple steps in activating the NF-kappaB signaling pathway. IL-1beta treatment induced degradation of the NF-kappaB inhibitory protein Ikappa-Balpha followed by nuclear translocation and DNA binding of p65 NF-kappaB, which were unaffected by inhibition of GSK-3. However, induction of NF-kappaB-dependent transcriptional activity by IL-1beta and CSE was largely reduced upon GSK-3 inhibition by SB216763. Collectively, we demonstrate that CSE and IL-1beta activate airway smooth muscle cells to secrete the proinflammatory cytokines IL-8, eotaxin, and VEGF-A. Furthermore, we show that GSK-3 regulates the release of these cytokines induced by CSE and IL-1beta by promoting NF-kappaB-dependent gene transcription.