The p38 MAPK and NF-κB Pathways are Involved in Cyclic Compressive Force-induced IL-6 Secretion in MLO-Y4 Cells
ABSTRACT We previously revealed the involvement of extracellular regulated protein kinases 1/2 (ERK1/2) in interleukin-6 (IL-6) secretion induced by cyclic compressive force (CCF) in MLO-Y4 cells. In this study, we investigated the contributions of the p38 mitogen-activated protein kinase (MAPK) and...
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Instituto de Tecnologia do Paraná (Tecpar)
2018-11-01
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Series: | Brazilian Archives of Biology and Technology |
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Online Access: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132018000100437&lng=en&tlng=en |
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author | Xiwen Chen Wenchuan Chen Yun He Yixin Zhang Chenfeng Chen Zhimin Zhu Hang Wang |
author_facet | Xiwen Chen Wenchuan Chen Yun He Yixin Zhang Chenfeng Chen Zhimin Zhu Hang Wang |
author_sort | Xiwen Chen |
collection | DOAJ |
description | ABSTRACT We previously revealed the involvement of extracellular regulated protein kinases 1/2 (ERK1/2) in interleukin-6 (IL-6) secretion induced by cyclic compressive force (CCF) in MLO-Y4 cells. In this study, we investigated the contributions of the p38 mitogen-activated protein kinase (MAPK) and nuclear factor-κB (NF-κB) pathways to IL-6 secretion by stimulating MLO-Y4 cells with CCF. At 80% confluence, different magnitudes (1000μstrain, 2000 μstrain and 4000 μstrain), frequencies (0.5 Hz, 1.0 Hz and 2.0 Hz) and durations (10 min, 30 min, 1 h, 3 h and 6 h) of CCF were loaded onto cells using a four-point bending system. Flow Cytometry (FCM) analysis was used to analyze cell mortality rates after CCF loading. p38 and p65 phosphorylation as well as IκBα degradation in MLO-Y4 cells were detected by Western blotting (WB). Changes in IL-6 secretion after inhibitor treatment were assessed by enzyme-linked immunosorbent assays (ELISAs). Cellular viability was over 90 percent after CCF. p38 and p65 phosphorylation increased under all conditions, whereas IκBα protein levels decreased. However, phosphorylation and degradation were not completely dependent on the loading magnitude, frequency or duration. Furthermore, p38 inhibition using the specific inhibitor SB203580 reduced both p38 phosphorylation and IL-6 secretion. Similarly, NF-κB inhibition using BAY 11-7082 decreased p65 phosphorylation and IL-6 secretion but increased the concentration of IκBα. These findings reveal significant roles for the p38 and NF-κB signaling pathways in IL-6 secretion induced by CCF in MLO-Y4 cells. |
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format | Article |
id | doaj.art-80af0cf2a6f94c318db4218e771afa00 |
institution | Directory Open Access Journal |
issn | 1678-4324 |
language | English |
last_indexed | 2024-04-13T12:39:04Z |
publishDate | 2018-11-01 |
publisher | Instituto de Tecnologia do Paraná (Tecpar) |
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series | Brazilian Archives of Biology and Technology |
spelling | doaj.art-80af0cf2a6f94c318db4218e771afa002022-12-22T02:46:34ZengInstituto de Tecnologia do Paraná (Tecpar)Brazilian Archives of Biology and Technology1678-43242018-11-0161010.1590/1678-4324-2018170777S1516-89132018000100437The p38 MAPK and NF-κB Pathways are Involved in Cyclic Compressive Force-induced IL-6 Secretion in MLO-Y4 CellsXiwen ChenWenchuan ChenYun HeYixin ZhangChenfeng ChenZhimin ZhuHang WangABSTRACT We previously revealed the involvement of extracellular regulated protein kinases 1/2 (ERK1/2) in interleukin-6 (IL-6) secretion induced by cyclic compressive force (CCF) in MLO-Y4 cells. In this study, we investigated the contributions of the p38 mitogen-activated protein kinase (MAPK) and nuclear factor-κB (NF-κB) pathways to IL-6 secretion by stimulating MLO-Y4 cells with CCF. At 80% confluence, different magnitudes (1000μstrain, 2000 μstrain and 4000 μstrain), frequencies (0.5 Hz, 1.0 Hz and 2.0 Hz) and durations (10 min, 30 min, 1 h, 3 h and 6 h) of CCF were loaded onto cells using a four-point bending system. Flow Cytometry (FCM) analysis was used to analyze cell mortality rates after CCF loading. p38 and p65 phosphorylation as well as IκBα degradation in MLO-Y4 cells were detected by Western blotting (WB). Changes in IL-6 secretion after inhibitor treatment were assessed by enzyme-linked immunosorbent assays (ELISAs). Cellular viability was over 90 percent after CCF. p38 and p65 phosphorylation increased under all conditions, whereas IκBα protein levels decreased. However, phosphorylation and degradation were not completely dependent on the loading magnitude, frequency or duration. Furthermore, p38 inhibition using the specific inhibitor SB203580 reduced both p38 phosphorylation and IL-6 secretion. Similarly, NF-κB inhibition using BAY 11-7082 decreased p65 phosphorylation and IL-6 secretion but increased the concentration of IκBα. These findings reveal significant roles for the p38 and NF-κB signaling pathways in IL-6 secretion induced by CCF in MLO-Y4 cells.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132018000100437&lng=en&tlng=eninterleukin-6cyclic compressive forcep38 mitogen-activated protein kinasesnuclear factor-κBosteocyte |
spellingShingle | Xiwen Chen Wenchuan Chen Yun He Yixin Zhang Chenfeng Chen Zhimin Zhu Hang Wang The p38 MAPK and NF-κB Pathways are Involved in Cyclic Compressive Force-induced IL-6 Secretion in MLO-Y4 Cells Brazilian Archives of Biology and Technology interleukin-6 cyclic compressive force p38 mitogen-activated protein kinases nuclear factor-κB osteocyte |
title | The p38 MAPK and NF-κB Pathways are Involved in Cyclic Compressive Force-induced IL-6 Secretion in MLO-Y4 Cells |
title_full | The p38 MAPK and NF-κB Pathways are Involved in Cyclic Compressive Force-induced IL-6 Secretion in MLO-Y4 Cells |
title_fullStr | The p38 MAPK and NF-κB Pathways are Involved in Cyclic Compressive Force-induced IL-6 Secretion in MLO-Y4 Cells |
title_full_unstemmed | The p38 MAPK and NF-κB Pathways are Involved in Cyclic Compressive Force-induced IL-6 Secretion in MLO-Y4 Cells |
title_short | The p38 MAPK and NF-κB Pathways are Involved in Cyclic Compressive Force-induced IL-6 Secretion in MLO-Y4 Cells |
title_sort | p38 mapk and nf κb pathways are involved in cyclic compressive force induced il 6 secretion in mlo y4 cells |
topic | interleukin-6 cyclic compressive force p38 mitogen-activated protein kinases nuclear factor-κB osteocyte |
url | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132018000100437&lng=en&tlng=en |
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