Abstract
The tissue inhibitor of the metalloproteinase-3 (TIMP-3) gene was isolated as a gene involved in the process of ascorbate-induced differentiation of mouse MC3T3-E1 cells by the differential display method. The functional roles of TIMP-3 were characterized by establishing stable cell lines, which constitutively expressed the TIMP-3 gene. The TIMP-3 transfectants produced type I collagen at the same level as that of normal cells in response to ascorbic acid 2-phosphate (AscP). However, the expression of the other osteoblastic marker proteins such as alkaline phosphatase (ALPase), osteopontin (OP), osteocalcin (OC), osteonectin (ON) and matrix metalloproteinases (MMPs) remained at a low level even in the presence of AscP. Furthermore, no mineralization of the extracellular matrix (ECM) occurred with the transfectants. Remodeling ECM through TIMPs and MMPs is concluded to be required for osteoblastic differentiation.
MeSH terms
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3T3 Cells
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Alkaline Phosphatase / biosynthesis
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Animals
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Ascorbic Acid / analogs & derivatives
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Ascorbic Acid / pharmacology*
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Biomarkers / analysis
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Cell Differentiation / drug effects
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Collagen / biosynthesis
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Extracellular Matrix / metabolism
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Gelatinases / metabolism
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Gene Expression / drug effects
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Matrix Metalloproteinases / biosynthesis
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Mice
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Osteoblasts / cytology
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Osteoblasts / drug effects*
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Osteoblasts / enzymology*
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Osteoblasts / metabolism
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Osteocalcin / biosynthesis
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Osteonectin / biosynthesis
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Osteopontin
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RNA, Messenger / biosynthesis
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Sialoglycoproteins / biosynthesis
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Tissue Inhibitor of Metalloproteinase-3 / genetics
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Tissue Inhibitor of Metalloproteinase-3 / metabolism
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Tissue Inhibitor of Metalloproteinase-3 / physiology*
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Transfection
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Up-Regulation
Substances
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Biomarkers
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Osteonectin
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RNA, Messenger
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Sialoglycoproteins
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Spp1 protein, mouse
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Tissue Inhibitor of Metalloproteinase-3
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Osteocalcin
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Osteopontin
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Collagen
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Alkaline Phosphatase
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Gelatinases
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Matrix Metalloproteinases
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Ascorbic Acid