Statins inhibit osteoblast migration by inhibiting Rac-Akt signaling

被引:45
作者
Fukuyama, R
Fujita, T
Azuma, Y
Hirano, A
Nakamuta, H
Koida, M
Komori, T
机构
[1] Osaka Univ, Dept Mol Med, Grad Sch Med, Suita, Osaka 5650871, Japan
[2] Osaka Dent Univ, Dept Pharmacol, Hirakata, Osaka 5731121, Japan
[3] Setsunan Univ, Fac Pharmaceut Sci, Dept Pharmacol, Hirakata, Osaka 5730101, Japan
关键词
chemotaxis; osteoblast migration; statin; Rae; Akt; PDGF; HMG-CoA reductase; Rho family; geranylgeranylation;
D O I
10.1016/j.bbrc.2004.01.104
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:636 / 642
页数:7
相关论文
共 40 条
  • [1] DISCOVERY, BIOCHEMISTRY AND BIOLOGY OF LOVASTATIN
    ALBERTS, AW
    [J]. AMERICAN JOURNAL OF CARDIOLOGY, 1988, 62 (15) : J10 - J15
  • [2] A role for Cdc42 in macrophage chemotaxis
    Allen, WE
    Zicha, D
    Ridley, AJ
    Jones, GE
    [J]. JOURNAL OF CELL BIOLOGY, 1998, 141 (05) : 1147 - 1157
  • [3] Endomorphin-2 modulates productions of TNF-α, IL-1β, IL-10, and IL-12, and alters functions related to innate immune of macrophages
    Azuma, Y
    Ohura, K
    [J]. INFLAMMATION, 2002, 26 (05) : 223 - 232
  • [4] Motility and invasion are differentially modulated by Rho family GTPases
    Banyard, J
    Anand-Apte, B
    Symons, M
    Zetter, BR
    [J]. ONCOGENE, 2000, 19 (04) : 580 - 591
  • [5] Ras and Rho GTPases: A family reunion
    Bar-Sagi, D
    Hall, A
    [J]. CELL, 2000, 103 (02) : 227 - 238
  • [6] CANALIS E, 1991, ANNU REV MED, V42, P17, DOI 10.1146/annurev.med.42.1.17
  • [7] HMG-CoA reductase inhibitors (statins) increase endothelial progenitor cells via the PI 3-kinase/Akt pathway
    Dimmeler, S
    Aicher, A
    Vasa, M
    Mildner-Rihm, C
    Adler, K
    Tiemann, M
    Rütten, H
    Fichtlscherer, S
    Martin, H
    Zeiher, AM
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2001, 108 (03) : 391 - 397
  • [8] Induction of osteoclast differentiation by Runx2 through receptor activator of nuclear factor-κB ligand (RANKL) and osteoprotegerin regulation and partial rescue of osteoclastogenesis in Runx2-/- mice by RANKL transgene
    Enomoto, H
    Shiojiri, S
    Hoshi, K
    Furuichi, T
    Fukuyama, R
    Yoshida, CA
    Kanatani, N
    Nakamura, R
    Mizuno, A
    Zanma, A
    Yano, K
    Yasuda, H
    Higashio, K
    Takada, K
    Komori, T
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (26) : 23971 - 23977
  • [9] Akt mediates cytoprotection of endothelial cells by vascular endothelial growth factor in an anchorage-dependent manner
    Fujio, Y
    Walsh, K
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (23) : 16349 - 16354
  • [10] New signaling pathway for parathyroid hormone and cyclic AMP action on extracellular-regulated kinase and cell proliferation in bone cells - Checkpoint of modulation by cyclic AMP
    Fujita, T
    Meguro, T
    Fukuyama, R
    Nakamuta, H
    Koida, M
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (25) : 22191 - 22200