TY - JOUR
T1 - Expression patterns of βig-h3 in chondrocyte differentiation during endochondral ossification
AU - Han, Min Su
AU - Kim, Jung Eun
AU - Shin, Hong In
AU - Kim, In San
PY - 2008/8/31
Y1 - 2008/8/31
N2 - 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 prehypertro-phic 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.
AB - 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 prehypertro-phic 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.
KW - Cell differentiation
KW - Chondrocytes
KW - Osteogenesis
KW - Transforming growth factor-β
UR - http://www.scopus.com/inward/record.url?scp=51949095469&partnerID=8YFLogxK
U2 - 10.3858/emm.2008.40.4.453
DO - 10.3858/emm.2008.40.4.453
M3 - Article
C2 - 18779658
AN - SCOPUS:51949095469
SN - 1226-3613
VL - 40
SP - 453
EP - 460
JO - Experimental and Molecular Medicine
JF - Experimental and Molecular Medicine
IS - 4
ER -