MISC

2004年3月

Statins inhibit osteoblast migration by inhibiting Rac-Akt signaling

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
  • R Fukuyama
  • ,
  • T Fujita
  • ,
  • Y Azuma
  • ,
  • A Hirano
  • ,
  • H Nakamuta
  • ,
  • M Koida
  • ,
  • T Komori

315
3
開始ページ
636
終了ページ
642
記述言語
英語
掲載種別
DOI
10.1016/j.bbrc.2004.01.104
出版者・発行元
ACADEMIC PRESS INC ELSEVIER SCIENCE

Cell migration is a key event in repair and remodeling of skeletal tissues, but the mechanism of osteoblast migration has not been resolved. Statins, which are inhibitors of 3-hydroxy-3-methylglutaryl CoA reductase, increase bone. However, the effect of statins on osteoblast migration remains to be clarified. We investigated the effect of fluvastatin and mevastatin on platelet-derived growth factor (PDGF)-induced migration of osteoblastic MC3T3-E1 cells. PDGF promoted osteoblast migration, while the statins inhibited PDGF-induced migration, and mevalonate and geranylgeranylpyrophosphate but not farnesylpyrophosphate abolished the effect of statins. Dominant-negative Rac severely inhibited PDGF-induced osteoblast migration and reduced Akt phosphorylation. Further, fluvastatin reduced Akt phosphorylation and dominant-negative Akt inhibited PDGF-induced osteoblast migration. These results demonstrate that statins inhibit PDGF-induced ostcoblast migration and Rac-Akt signaling plays an important role in the ostcoblast migration, and suggest that statins restrain Rac function by inhibiting geranylgeranylation of Rac, which leads to the reduction in Akt activation and osteoblast migration. (C) 2004 Elsevier Inc. All rights reserved.

リンク情報
DOI
https://doi.org/10.1016/j.bbrc.2004.01.104
CiNii Articles
http://ci.nii.ac.jp/naid/80016515778
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/14975748
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000189291900017&DestApp=WOS_CPL
ID情報
  • DOI : 10.1016/j.bbrc.2004.01.104
  • ISSN : 0006-291X
  • CiNii Articles ID : 80016515778
  • PubMed ID : 14975748
  • Web of Science ID : WOS:000189291900017

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