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자료유형
학술저널
저자정보
저널정보
대한생화학·분자생물학회 Experimental and Molecular Medicine Experimental and Molecular Medicine 제40권 제4호
발행연도
2008.1
수록면
453 - 460 (8page)

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βig-h3 is a TGF-β-induced extracellular matrix protein which is expressed in many tissues including bones and cartilages. In previous reports, we showed that βig-h3 mediates cell adhesion and migration and, especially in bones, negatively regulates the mineralization in the end stage of endochondral ossification. Here, to elucidate the expression pattern and role of βig-h3 in chondrocyte differentiation, ATDC5 chondrocytes and embryonic and postnatal mice were used for in vitro differentiation studies and in vivo studies, respectively. βig-h3 was strongly induced by the treatment of TGF-β1 and the expression level of βig-h3 mRNA and protein were highly expressed in the early stages of differentiation but decreased in the late stages in ATDC5. Furthermore, the patterns of TGF-β1, -β2, and -β3 mRNA expression were concurrent with βig-h3 in ATDC5. βig-h3 was deeply stained in perichondrium (PC), periosteum (PO), and prehypertrophic chondrocytes (PH) through the entire period of endochondral ossification in mice. βig-h3 was mainly expressed in PC and PH at embryonic days and obviously in PH in postnatal days. These results suggest that βig-h3 may play a critical role as a regulator of chondrogenic differentiation in endochondral ossification.

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