TY - JOUR
T1 - Negative Regulation of Chondrocyte Differentiation by Transcription Factor AP-2α
AU - Huang, Zhengmin
AU - Xu, Haiming
AU - Sandell, Linda
PY - 2004/2
Y1 - 2004/2
N2 - This study investigated the role of transcription factor AP-2α in chondrocyte differentiation in vitro. AP-2α mRNA declined during differentiation, and overexpression of AP-2α inhibited differentiation. The results demonstrated that AP-2α plays a negative role in chondrocyte differentiation. Introduction: Transcription factor AP-2α has been detected in growth plate and articular chondrocytes and has been shown to regulate cartilage matrix gene expression in vitro. However, the precise functional role of AP-2α in chondrocyte differentiation is not known. In this study, we assessed the expression and the function of AP-2α in chondrocyte differentiation of ATDC5 cells. Materials and Methods: Chondrocyte differentiation of ATDC5 cells was induced with insulin or transforming growth factor β (TGF-β). Proteoglycan production was assessed by alcian blue staining, and expression levels of chondrocyte marker genes and AP-2 gene family were determined by quantitative real time reverse transcriptasepolymerase chain reaction (RT-PCR). Overexpression of AP-2α in ATDC5 cells was accomplished by retroviral infection. Infected cells were selected for G418 resistance and pooled for further analysis. Results and Conclusions: Quantitative real time RT-PCR analysis showed that among the four members of the AP-2 gene family, AP-2α mRNA was the most abundant. AP-2α mRNA levels progressively declined during the differentiation induced by either insulin or TGF-β treatment. Retroviral expression of AP-2α in ATDC5 cells prevented the formation of cartilage nodules, suppressed the proteoglycan production, and inhibited the expression of type II collagen, aggrecan, and type X collagen. Expression profile analysis of key transcription factors involved in chondrogenesis showed that overexpression of AP-2α maintained the expression of Sox9 but suppressed the expression of Sox5 and Sox6. Taken together, we provide, for the first time, molecular and cellular evidence suggesting that AP-2α is a negative regulator of chondrocyte differentiation.
AB - This study investigated the role of transcription factor AP-2α in chondrocyte differentiation in vitro. AP-2α mRNA declined during differentiation, and overexpression of AP-2α inhibited differentiation. The results demonstrated that AP-2α plays a negative role in chondrocyte differentiation. Introduction: Transcription factor AP-2α has been detected in growth plate and articular chondrocytes and has been shown to regulate cartilage matrix gene expression in vitro. However, the precise functional role of AP-2α in chondrocyte differentiation is not known. In this study, we assessed the expression and the function of AP-2α in chondrocyte differentiation of ATDC5 cells. Materials and Methods: Chondrocyte differentiation of ATDC5 cells was induced with insulin or transforming growth factor β (TGF-β). Proteoglycan production was assessed by alcian blue staining, and expression levels of chondrocyte marker genes and AP-2 gene family were determined by quantitative real time reverse transcriptasepolymerase chain reaction (RT-PCR). Overexpression of AP-2α in ATDC5 cells was accomplished by retroviral infection. Infected cells were selected for G418 resistance and pooled for further analysis. Results and Conclusions: Quantitative real time RT-PCR analysis showed that among the four members of the AP-2 gene family, AP-2α mRNA was the most abundant. AP-2α mRNA levels progressively declined during the differentiation induced by either insulin or TGF-β treatment. Retroviral expression of AP-2α in ATDC5 cells prevented the formation of cartilage nodules, suppressed the proteoglycan production, and inhibited the expression of type II collagen, aggrecan, and type X collagen. Expression profile analysis of key transcription factors involved in chondrogenesis showed that overexpression of AP-2α maintained the expression of Sox9 but suppressed the expression of Sox5 and Sox6. Taken together, we provide, for the first time, molecular and cellular evidence suggesting that AP-2α is a negative regulator of chondrocyte differentiation.
KW - AP-2α
KW - ATDC5 cells
KW - Cartilage matrix protein
KW - Chondrogenesis
KW - Differentiation
UR - http://www.scopus.com/inward/record.url?scp=1642485846&partnerID=8YFLogxK
U2 - 10.1359/jbmr.2004.19.2.245
DO - 10.1359/jbmr.2004.19.2.245
M3 - Article
C2 - 14969394
AN - SCOPUS:1642485846
SN - 0884-0431
VL - 19
SP - 245
EP - 255
JO - Journal of Bone and Mineral Research
JF - Journal of Bone and Mineral Research
IS - 2
ER -