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Interleukin-6 family cytokines: signaling and effects in human airway smooth muscle cells
被引:37
作者:
Lahiri, T
Laporte, JD
Moore, PE
Panettieri, RA
Shore, SA
机构:
[1] Harvard Univ, Sch Publ Hlth, Physiol Program, Boston, MA 02115 USA
[2] Univ Penn, Sch Med, Dept Med, Div Pulm & Crit Care, Philadelphia, PA 19104 USA
关键词:
oncostatin;
cyclooxygenase;
prostaglandin;
signal transducer and activator of transcription;
D O I:
10.1152/ajplung.2001.280.6.L1225
中图分类号:
Q4 [生理学];
学科分类号:
071003 ;
摘要:
Interleukin (IL)-1 beta induces cyclooxygenase (COX)-2 expression and prostanoid formation in cultured human airway smooth muscle (HASM) cells. In other cell types, IL-6 family cytokines induce COX-2 or augment IL-1 beta -induced COX-2 expression. The purpose of this study was to determine whether IL-6 family cytokines were involved in COX-2 expression in HASM cells. RT-PCR was used to demonstrate that the necessary receptor components for IL-6-type cytokine binding are expressed in HASM cells. IL-6 and oncostatin M (OSM) each caused a dose-dependent phosphorylation of signal transducer and activator of transcription-3, whereas IL-11 did not. IL-6, IL-11, and OSM alone had no effect on COX-2 expression. However, OSM caused dose-dependent augmentation of COX-2 expression and prostaglandin (PG) E-2 release induced by IL-1 beta. In contrast, IL-6 and IL-11 did not alter IL-1 beta -induced COX-2 expression. IL-6 did increase IL-1 beta -induced PGE(2) formation in unstimulated cells but not in cells stimulated with arachidonic acid (AA; 10(-5) M), suggesting that IL-6 effects were mediated at the level of AA release. Our results indicate that IL-6 and OSM are capable of inducing signaling in HASM cells. In addition, OSM and IL-1 beta synergistically cause COX-2 expression and PGE(2) release.
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页码:L1225 / L1232
页数:8
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