کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1931299 | 1050548 | 2010 | 5 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: ERK1/2 is involved in cyclic compressive force-induced IL-6 secretion in MLO-Y4 cells ERK1/2 is involved in cyclic compressive force-induced IL-6 secretion in MLO-Y4 cells](/preview/png/1931299.png)
We previously reported that cyclic compressive force (CCF) induced interleukin-6 mRNA expression in osteocyte-like MLO-Y4 cells. But little is known about how the stimuli are converted into the biochemical signals in MLO-Y4 cells. The aim of this research was to study the effect of CCF on the IL-6 secretion and the role of extracellular signal-regulated kinases 1/2 (ERK1/2) in this process. The cells were exposed to CCF with different magnitudes (1000, 2000 and 4000 μstrain), frequencies (0.5, 1.0 and 2.0 Hz) and durations (10 min, 30 min, 1 h, 3 h and 6 h) by a four-point bending system. The IL-6 secretion and ERK1/2 phosphorylation of the cells were determined by ELISA and Western blotting, respectively. The results showed that IL-6 protein secretion was significantly up-regulated in response to CCF in a magnitude-, frequency- and duration-dependent fashion. The phosphorylation of ERK1/2 also increased in all cases but not depended on the magnitude, frequency or duration of CCF. Furthermore, the inhibition of the ERK1/2 pathway by its specific inhibitor PD098059 decreased but not completely abrogated the IL-6 secretion from stressed MLO-Y4 cells. These findings demonstrate that CCF-induced IL-6 secretion occurs via a mechanism that involves ERK1/2 signaling pathway and suggest that modulation of this event contributes to the pathogenesis of osteoporosis and stress-induced pathological bone resorption as well.
Research highlights
► Cyclic compressive force (CCF) could induce IL-6 secretion in osteocyte-like cells.
► The IL-6 secretion depended on the magnitude, frequency and duration of CCF.
► ERK1/2 was involved in the CCF-induced IL-6 secretion in the cells.
Journal: Biochemical and Biophysical Research Communications - Volume 401, Issue 3, 22 October 2010, Pages 339–343