Characterization of osteoblastic differentiation of stromal cell line ST2 that is induced by ascorbic acid

被引:127
作者
Otsuka, E
Yamaguchi, A
Hirose, S
Hagiwara, H
机构
[1] Tokyo Inst Technol, Res Ctr Expt Biol, Midori Ku, Yokohama, Kanagawa 2268501, Japan
[2] Tokyo Inst Technol, Dept Biol Sci, Yokohama, Kanagawa 2268501, Japan
[3] Nagasaki Univ, Sch Dent, Dept Oral Pathol, Nagasaki 8528588, Japan
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 1999年 / 277卷 / 01期
关键词
ST2; cell; osteoblast; type I collagen; alkaline phosphatase; bone morphogenetic protein;
D O I
10.1152/ajpcell.1999.277.1.C132
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The stromal cell line ST2, derived from mouse bone marrow differentiated into osteoblast-like cells in response to ascorbic acid. Ascorbic acid induced alkaline phosphatase (ALPase) activity, the expression of mRNAs for proteins that are markers of osteoblastic differentiation, the deposition of calcium, and the formation of mineralized nodules by ST2 cells. We investigated the mechanism whereby ascorbic acid induced the differentiation of ST2 cells. Inhibitors of the formation of collagen triple helices completely blocked the effects of ascorbic acid on ST2 cells, an indication that matrix formation by type I collagen is essential for the induction of osteoblastic differentiation of ST2 cells by ascorbic acid. We furthermore examined the effects of bone morphogenetic proteins (BMPs) on the differentiation of ST2 cells induced by ascorbic acid. Ascorbic acid had no effect on the expression of mRNAs for BMP-4 and the BMP receptors. However, a soluble form of BMP receptor IA inhibited the induction of ALPase activity by ascorbic acid. These results suggest that ascorbic acid might promote the differentiation of ST2 cells into osteoblast-like cells by inducing the formation of a matrix of type I collagen, with subsequent activation of the signaling pathways that involve BMPs.
引用
收藏
页码:C132 / C138
页数:7
相关论文
共 25 条
[1]   FACTORS THAT PROMOTE PROGRESSIVE DEVELOPMENT OF THE OSTEOBLAST PHENOTYPE IN CULTURED FETAL-RAT CALVARIA CELLS [J].
ARONOW, MA ;
GERSTENFELD, LC ;
OWEN, TA ;
TASSINARI, MS ;
STEIN, GS ;
LIAN, JB .
JOURNAL OF CELLULAR PHYSIOLOGY, 1990, 143 (02) :213-221
[2]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[3]   INTEGRINS AND SIGNAL-TRANSDUCTION PATHWAYS - THE ROAD TAKEN [J].
CLARK, EA ;
BRUGGE, JS .
SCIENCE, 1995, 268 (5208) :233-239
[4]  
FRANCESCHI RT, 1992, NUTR REV, V50, P65
[5]  
FRANCESCHI RT, 1992, J BONE MINER RES, V7, P235
[6]  
FRANCESCHI RT, 1994, J BONE MINER RES, V9, P843
[7]   EXPRESSION OF DIFFERENTIATED FUNCTION BY MINERALIZING CULTURES OF CHICKEN OSTEOBLASTS [J].
GERSTENFELD, LC ;
CHIPMAN, SD ;
GLOWACKI, J ;
LIAN, JB .
DEVELOPMENTAL BIOLOGY, 1987, 122 (01) :49-60
[8]   cGMP produced in response to ANP and CNP regulates proliferation and differentiation of osteoblastic cells [J].
Hagiwara, H ;
Inoue, A ;
Yamaguchi, A ;
Yokose, S ;
Furuya, M ;
Tanaka, S ;
Hirose, S .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1996, 270 (05) :C1311-C1318
[9]   Bone morphogenetic proteins in development [J].
Hogan, BLM .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1996, 6 (04) :432-438
[10]   BONE MORPHOGENETIC PROTEIN-2 CONVERTS THE DIFFERENTIATION PATHWAY OF C2C12 MYOBLASTS INTO THE OSTEOBLAST LINEAGE [J].
KATAGIRI, T ;
YAMAGUCHI, A ;
KOMAKI, M ;
ABE, E ;
TAKAHASHI, N ;
IKEDA, T ;
ROSEN, V ;
WOZNEY, JM ;
FUJISAWASEHARA, A ;
SUDA, T .
JOURNAL OF CELL BIOLOGY, 1994, 127 (06) :1755-1766