Activation of the FGF signaling pathway and subsequent induction of mesenchymal stem cell differentiation by inorganic polyphosphate

被引:64
作者
Kawazoe, Yumi [1 ,2 ]
Katoh, Shinichi [1 ]
Onodera, Yuichiro [2 ]
Kohgo, Takao [2 ]
Shindoh, Masanobu [2 ]
Shiba, Toshikazu [1 ]
机构
[1] Regenetiss Inc, Tokyo 1910065, Japan
[2] Hokkaido Univ, Grad Sch Dent Med, Sapporo, Hokkaido 0608586, Japan
来源
INTERNATIONAL JOURNAL OF BIOLOGICAL SCIENCES | 2008年 / 4卷 / 01期
关键词
inorganic polyphosphate; FGF; osteogenic differentiation; cell calcification; mesenchymal stem cell; dental pulp cell;
D O I
10.7150/ijbs.4.37
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
Inorganic polyphosphate [poly( P)] is a biopolymer existing in almost all cells and tissues, although its biological functions in higher eukaryotes have not been completely elucidated. We previously demonstrated that poly( P) enhances the function of fibroblast growth factors (FGFs) by stabilizing them and strengthening the affinity between FGFs and their cell surface receptors. Since FGFs play crucial roles in bone regeneration, we further investigated the effect of poly( P) on the cell differentiation of human stem cells via FGF signaling systems. Human dental pulp cells (HDPCs) isolated from human dental pulp show the characteristics of multipotent mesenchymal stem cells (MSCs). HDPCs secreted FGFs and the proliferation of HDPCs was shown to be enhanced by treatment with poly( P). Cell surface receptor-bound FGF-2 was stably maintained for more than 40 hours in the presence of poly( P). The phosphorylation of ERK1/2 was also enhanced by poly( P). The effect of poly( P) on the osteogenic differentiation of HDPCs and human MSCs (hMSCs) were also investigated. After 5 days of treatment with poly( P), type-I collagen expression of both cell types was enhanced. The C-terminal peptide of type-I collagen was also released at higher levels in poly(P)- treated HDPCs. Microarray analysis showed that expression of matrix metalloproteinase-1 (MMP1),osteopontin (OPN), osteocalcin (OC) and osteoprotegerin was induced in both cell types by poly(P). Furthermore, induced expression of MMP1, OPN and OC genes in both cells was confirmed by real-time PCR. Calcification of both cell types was clearly observed by alizarin red staining following treatment with poly( P). The results suggest that the activation of the FGF signaling pathway by poly( P) induces both proliferation and mineralization of stem cells.
引用
收藏
页码:37 / 47
页数:11
相关论文
共 37 条
[31]  
Tang KT, 1996, J CELL BIOCHEM, V61, P152, DOI 10.1002/(SICI)1097-4644(19960401)61:1<152::AID-JCB16>3.0.CO
[32]  
2-Q
[33]   Retention of multilineage differentiation potential of mesenchymal cells during proliferation in response to FGF [J].
Tsutsumi, S ;
Shimazu, A ;
Miyazaki, K ;
Pan, H ;
Koike, C ;
Yoshida, E ;
Takagishi, K ;
Kato, Y .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 288 (02) :413-419
[34]   BASIC FIBROBLAST GROWTH-FACTOR STIMULATES EXPRESSION OF INTERSTITIAL COLLAGENASE AND INHIBITORS OF METALLOPROTEINASES IN RAT BONE-CELLS [J].
VARGHESE, S ;
RAMSBY, ML ;
JEFFREY, JJ ;
CANALIS, E .
ENDOCRINOLOGY, 1995, 136 (05) :2156-2162
[35]   BIOLOGICAL ASPECTS OF INORGANIC POLYPHOSPHATES [J].
WOOD, HG ;
CLARK, JE .
ANNUAL REVIEW OF BIOCHEMISTRY, 1988, 57 :235-260
[36]   Fibroblast growth factor 2 induction of the osteocalcin gene requires MAPK activity and phosphorylation of the osteoblast transcription factor, Cbfa1/Runx2 [J].
Xiao, GZ ;
Jiang, D ;
Gopalakrishnan, R ;
Franceschi, RT .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (39) :36181-36187
[37]   Effects of recombinant human fibroblast growth factor-2 on osteogenic cell populations during orthopic osteogenesis in vivo [J].
Zellin, G ;
Linde, A .
BONE, 2000, 26 (02) :161-168