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      Cbfa1 is a positive regulatory factor in chondrocyte maturation.

      The Journal of Biological Chemistry
      Animals, Cell Differentiation, drug effects, Chick Embryo, Chondrocytes, cytology, metabolism, Core Binding Factor Alpha 1 Subunit, DNA, Complementary, genetics, DNA-Binding Proteins, biosynthesis, classification, Hypertrophy, Mice, Neoplasm Proteins, Oligonucleotides, Antisense, pharmacology, Osteoblasts, Phenotype, RNA, Messenger, analysis, Tibia, Transcription Factor AP-2, Transcription Factors

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          Abstract

          Cbfa1 is a transcription factor that belongs to the runt domain gene family. Cbfa1-deficient mice showed a complete lack of bone formation due to the maturational arrest of osteoblasts, demonstrating that Cbfa1 is an essential factor for osteoblast differentiation. Further, chondrocyte maturation was severely disturbed in Cbfa1-deficient mice. In this study, we examined the possibility that Cbfa1 is also involved in the regulation of chondrocyte differentiation. mRNAs for both Cbfa1 isotypes, type I Cbfa1 (Pebp2alphaA/Cbfa1) and type II Cbfa1 (Osf2/Cbfa1 or til-1), which are different in N-terminal domain, were expressed in terminal hypertrophic chondrocytes as well as osteoblasts. In addition, mRNA for type I Cbfa1 was expressed in other hypertrophic chondrocytes and prehypertrophic chondropcytes. In a chondrogenic cell line, ATDC5, the expression of type I Cbfa1 was elevated prior to differentiation to the hypertrophic phenotype, which is characterized by type X collagen expression. Treatment with antisense oligonucleotides for type I Cbfa1 severely reduced type X collagen expression in ATDC5 cells. Retrovirally forced expression of either type I or type II Cbfa1 in chick immature chondrocytes induced type X collagen and MMP13 expression, alkaline phosphatase activity, and extensive cartilage-matrix mineralization. These results indicate that Cbfa1 is an important regulatory factor in chondrocyte maturation.

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