Induction of calcification in MC3T3-E1 cells by inorganic polyphosphate

被引:80
作者
Kawazoe, Y
Shiba, T
Nakamura, R
Mizuno, A
Tsutsumi, K
Uematsu, T
Yamaoka, M
Shindoh, M
Kohgo, T
机构
[1] Regenetiss Co Ltd, Nagano 3940002, Japan
[2] Fujirebio Inc, Frontier Res Div, Tokyo, Japan
[3] Hokkaido Univ, Grad Sch Dent Med, Sapporo, Hokkaido, Japan
[4] Hokkaido Univ, Grad Sch Engn, Sapporo, Hokkaido, Japan
[5] Matsumoto Dent Univ, Nagano, Japan
关键词
calcification; osteoblasts; osteopontin; osteocalcin; polyphosphate;
D O I
10.1177/154405910408300806
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Relatively large amounts of inorganic polyphosphate [poly(P)] (400 muM) have been found in normal osteoblasts. The effect of poly( P) with an average chain length of 65 phosphate residues on cell calcification was therefore investigated with the use of MC3T3-E1 cells. Expression of both osteopontin and osteocalcin was induced by poly(P) (0.1 similar to 1 mM), and cells treated with poly(P) were strongly stained by alizarin red. In addition, the level of alkaline phosphatase activity induced in poly(P)-treated cells was two-fold higher than that in either orthophosphate-treated or control cells but not higher than that in cells treated with beta-glycerophosphate and ascorbic acid. In contrast, however, polyphosphatase activities were activated by poly(P) treatment to levels up to sixfold greater than that in controls. MC3T3-E1 cells may utilize poly(P) as a phosphate source for calcification rather than phosphate sources that are mainly produced by ALPase. Poly(P)-dependent induction of polyphosphatase activities may therefore promote calcification in MC3T3-E1 cells.
引用
收藏
页码:613 / 618
页数:6
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