Roles of MAP kinases in the regulation of bone matrix gene expressions in human osteoblasts by oscillatory fluid flow
We investigated the effects of oscillatory flow in regulating the gene expressions of type I collagen (COL1, the main component of human bone tissues) and osteopontin (OPN, the key gene for calcium deposition) in human osteoblast‐like (MG‐63) cells, and the roles of mitogen‐activated protein kinases...
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Published in: | Journal of cellular biochemistry Vol. 98; no. 3; pp. 632 - 641 |
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Main Authors: | , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Hoboken
Wiley Subscription Services, Inc., A Wiley Company
01-06-2006
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Subjects: | |
Online Access: | Get full text |
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Summary: | We investigated the effects of oscillatory flow in regulating the gene expressions of type I collagen (COL1, the main component of human bone tissues) and osteopontin (OPN, the key gene for calcium deposition) in human osteoblast‐like (MG‐63) cells, and the roles of mitogen‐activated protein kinases (MAPKs) in this regulation. The cells were subjected to oscillatory flow (0.5 ± 4 dyn/cm2) or kept under static condition for various time periods (15 min, 30 min, 1 h, 2 h, 4 h, 8 h, and 16 h). Oscillatory flow caused significant up‐regulations of both COL1 and OPN gene expressions over the 16 h of study, and a transient activation of MAPKs was starting at 15 min and declining to basal level in 2 h. The flow‐induction of COL1 was blocked by an ERK inhibitor (PD98059) and reduced by a JNK inhibitor (SP600125), whereas that of OPN was abolished by PD98059. Analysis of the cis‐elements in the COL1 and OPN promoters suggests the involvement of transacting factors Elk‐1 and AP‐1 in the transcription regulation. The ERK inhibitor (PD98059) blocked Elk‐1 phosphorylation, as well as COL1 and OPN gene expression. The JNK inhibitor (SP600125) abolished c‐jun phosphorylation and COL1 expression. These results suggest that the flow‐induction of OPN was mediated through the ERK‐Elk1‐OPN pathway, and that COL1 was regulated by both the ERK‐Elk1‐COL1 and JNK‐c‐JUN‐COL1 pathway. J. Cell. Biochem. 98: 632–641, 2006. © 2006 Wiley‐Liss, Inc. |
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Bibliography: | istex:AF9E7B97BF330E51BDE567354BBB8CD7E469E18C ArticleID:JCB20697 ark:/67375/WNG-S2DC4FTV-C NIH (SC) (to Fong-Chin Su) - No. HL19454; No. HL43026; No. HL080518; No. HL64382 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0730-2312 1097-4644 |
DOI: | 10.1002/jcb.20697 |