共 24 条
FGF2 stimulates the proliferation of human mesenchymal stem cells through the transient activation of JNK signaling
被引:84
作者:

Ahn, Hee-Jin
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机构:
CHA Univ, Grad Sch, Dept Biomed Sci, Gyeonggi Do 487010, South Korea CHA Univ, Grad Sch, Dept Biomed Sci, Gyeonggi Do 487010, South Korea

Lee, Woo-Jung
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CHA Univ, Grad Sch, Dept Biomed Sci, Gyeonggi Do 487010, South Korea CHA Univ, Grad Sch, Dept Biomed Sci, Gyeonggi Do 487010, South Korea

Kwack, KyuBum
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CHA Univ, Grad Sch, Dept Biomed Sci, Gyeonggi Do 487010, South Korea CHA Univ, Grad Sch, Dept Biomed Sci, Gyeonggi Do 487010, South Korea

Do Kwon, Young
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机构:
CHA Univ, Grad Sch, Dept Biomed Sci, Gyeonggi Do 487010, South Korea CHA Univ, Grad Sch, Dept Biomed Sci, Gyeonggi Do 487010, South Korea
机构:
[1] CHA Univ, Grad Sch, Dept Biomed Sci, Gyeonggi Do 487010, South Korea
关键词:
Mesenchymal stem cell;
FGF2;
c-Jun N-terminal kinase;
Proliferation;
Differentiation potential;
N-TERMINAL KINASE;
MARROW STROMAL CELLS;
FIBROBLAST-GROWTH-FACTOR-2;
MECHANISMS;
APOPTOSIS;
D O I:
10.1016/j.febslet.2009.07.056
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:
FGF2 has been shown to enhance proliferation and maintain differentiation potential in hMSCs during in vitro propagation. In this study, we investigated the role of mitogen-activated protein kinase in the functions of FGF2 in hMSCs. We demonstrated that FGF2 induces the transient activation of c-Jun N-terminal kinase (JNK), but not extracellular signal-regulated protein kinase or p38 protein kinase. SP600125 and a dominant negative JNK1 significantly reduced the FGF2-enhanced proliferation of hMSCs. Treatment with SP600125 also diminished the activity of FGF2 in the maintenance of adipogenic and osteogenic differentiation potential. These results suggest that JNK signaling is involved in the FGF2-induced stimulation of the proliferation and the maintenance of differentiation potential in hMSCs. (C) 2009 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
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页码:2922 / 2926
页数:5
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