Extracellular matrix regulates induction of alkaline phosphatase expression by ascorbic acid in human fibroblasts

被引:43
作者
Abe, T
Abe, Y
Aida, Y
Hara, Y
Maeda, K
机构
[1] Kyushu Univ, Fac Dent Sci, Div Oral Rehabil, Sect Periodontol,Higashi Ku, Fukuoka 8128582, Japan
[2] Kyushu Univ, Fac Dent Sci, Div Oral Rehabil, Sect Clin Oral Med Biol, Fukuoka 8128582, Japan
[3] Nagasaki Univ, Sch Dent, Dept Periodontol, Nagasaki 852, Japan
关键词
D O I
10.1002/jcp.10011
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
During wound healing and inflammation, fibroblasts express elevated alkaline phosphatase (ALP), but are not in contact with collagen fibrils in the fibronectin (FN)-rich granulation tissue. We hypothesized that the extracellular matrix (ECM) environment might influence the induction of ALP in fibroblasts, Here we tested this hypothesis by studying the ALP-inductive response of normal human gingival, p fibroblasts to ascorbic acid (AsA). AsA induced ALP activity and protein in cells in conventional monolayer culture. This induction was inhibited by blocking-antibodies to the FN receptor alpha5 beta1 integrin and by the proline analog 3,4-dehydroproline (DHP). DHP prevented cells from arranging FN fibrils into a pericellular network and reduced the activity of cell spreading on FN. Plating of cells on FN facilitated the up-regulation by AsA of ALP expression, but did not substitute for AsA. In contrast, AsA did not cause ALP induction in cells cultured on and in polymerized type I collagen gets. Collagen fibrils inhibited the upregulation by AsA of ALP expression in cells plated on FN. These results indicate that the ECM regulates the induction of ALP expression by AsA in fibroblasts: FN enables them to express ALP in response to AsA through interaction with integrin alpha5 beta1, whereas type I collagen fibrils cause the suppression of ALP expression and overcome FN. (C) 2001 Wiley-Liss, Inc.
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页码:144 / 151
页数:8
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