BONE MORPHOGENETIC PROTEIN-2 CAUSES COMMITMENT AND DIFFERENTIATION IN C3H10T1/2 AND 3T3 CELLS

被引:426
作者
WANG, EA
ISRAEL, DI
KELLY, S
LUXENBERG, DP
机构
[1] Developmental Biology, Genetics Institute, Cambridge, MA 02140
[2] Molecular and Cellular Genetics, Genetics Institute, Cambridge, MA 02140
关键词
BONE MORPHOGENETIC PROTEIN; DIFFERENTIATION; C3H10T1/2; ADIPOGENESIS; CHONDROGENESIS; OSTEOGENESIS;
D O I
10.3109/08977199308991582
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
C3H10T1/2 cells are an established mesenchymal stem cell line which can differentiate into muscle, fat and cartilage cells when treated with azacytidine. Bone morphogenetic protein-2 (BMP-2) caused a dose dependent differentiation of these cells into fat, cartilage and bone cells-low concentrations favoring adipocytes and high concentrations chondrocytes and osteoblasts. The differentiated phenotypes were stable in the absence of BMP-2. Furthermore, the addition of other growth factors during the differentiation process altered the frequency of the differentiated colony formation. Transfection of the C3H10T1/2 cells with a BMP-2 cDNA also induced a phenotypic change from the parental fibroblast to adipocytes and osteoblasts. Our results in this model system indicate that a single protein factor can cause differentiation of a stem cell line to multiple phenotypes, that phenotypes induced can be regulated by factor concentration, and that other factors can also influence BMP-2 induced differentiation.
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页码:57 / &
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