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Resveratrol enhances proliferation and osteoblastic differentiation in human mesenchymal stem cells via ER-dependent ERK1/2 activation
被引:235
作者:
Dai, Z.
Li, Y.
Quarles, L. D.
Song, T.
Pan, W.
Zhou, H.
Xiao, Z.
机构:
[1] Univ Kansas, Med Ctr, Kidney Inst, Kansas City, KS 66160 USA
[2] Cent S Univ, Inst Clin Pharmacol, Changsha 410078, Peoples R China
[3] Cent S Univ, Inst Reprod & Stem Cell Engn, Changsha 410078, Peoples R China
关键词:
resveratrol;
mesenchymal stem cell;
estrogen receptor;
ERK1/2;
p38;
MAPK;
D O I:
10.1016/j.phymed.2007.04.003
中图分类号:
Q94 [植物学];
学科分类号:
071001 ;
摘要:
In the present study, we investigated the in vitro effect of resveratrol (RSVL), a polyphenolic phytoestrogen, on cell proliferation and osteoblastic maturation in human bone marrow-derived mesenchymal stem cell (HBMSC) cultures. RSVL (10(-8)-10(-5)M) increased cell growth dose-dependently, as measured by [H-3]-thymidine incorporation, and stimulated osteoblastic maturation as assessed by alkaline phosphatase (ALP) activity, calcium deposition into the extracellular matrix, and the expression of osteoblastic markers such as RUNA2/CBFA1, Osterix and Osteocalcin in HBMSCs cell cultures. Further studies found that RSVL (10(-6) M) resulted in a rapid activation of both extracellular signal-regulated kinase 1/2 (ERK1/2) and p38 mitogen-activated protein kinase (MAPK) signaling in HBMSCs cultures. The effects of RSVL were mimicked by 17 beta-estrodial (10(-8) M) and were abolished by estrogen receptor (ER) antagonist ICI182780. An ERK1/2 pathway inhibitor, PD98059, significantly attenuated RSVL-induced ERK1/2 phosphorylation, consistent with the reduction of cell proliferation and osteoblastic differentiation as well as expression of osteoblastic markers. In contrast, SB203580, a p38 MAPK pathway blocker, blocked RSVL-induced p38 phosphorylation, but resulted in an increase of cell proliferation and a more osteoblastic maturation. These data suggest that RSVL stimulates HBMSCs proliferation and osteoblastic differentiation through an ER-dependent mechanism and coupling to ERK1/2 activation. (c) 2007 Elsevier GmbH. All rights reserved.
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页码:806 / 814
页数:9
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