TY - JOUR
T1 - Transcriptional induction of connective tissue growth factor/hypertrophic chondrocyte-specific 24 gene by dexamethasone in human chondrocytic cells
AU - Kubota, Satoshi
AU - Moritani, Norifumi H.
AU - Kawaki, Harumi
AU - Mimura, Haruyo
AU - Minato, Masanao
AU - Takigawa, Masaharu
N1 - Funding Information:
This work was supported in part by Grants-in-Aid for Scientific Research (S.K. and M.T.) and Exploratory Research (M.T.) from the Ministry of Education, Science, Sports, and Culture of Japan and by grants from the Research for the Future Programme of the Japan Society for the Promotion of Science (Project: Biological Tissue Engineering; contract grant number: JSPS-RFTF98100201) (M.T.), the Nakatomi Health Science Foundation (S.K.), the Foundation for Growth Science in Japan (M.T.), the Sumitomo Foundation (M.T.), and the Ryobi-teien Memorial Foundation (S.K.). The authors wish to thank Drs. Tohru Nakanishi, Kumiko Nawachi, Kyoji Nakao, and Morihiko Oka for helpful suggestions, Ms. Kazumi Oyama for technical assistance, and Ms. Yuki Nonami for secretarial assistance.
PY - 2003/10/1
Y1 - 2003/10/1
N2 - Connective tissue growth factor (CTGF/Hcs24) is a critical growth factor for chondrocytic growth and differentiation. In this report, we describe for the first time glucocorticoid-mediated induction of the CTGF/Hcs24 gene in a chondrocytic cell line, HCS-2/8. Steady-state mRNA levels of CTGF/Hcs24 were remarkably increased after treatment with 50 nM dexamethasone, as confirmed by Northern blotting and quantitative real-time polymerase chain reaction (PCR) analysis. Corresponding to the increase in mRNA, production of CTGF/Hcs24 protein was remarkably enhanced, following a time course of up to 6 h. The observed increase in mRNA can be ascribed to transcriptional enhancement, since the stability of CTGF/Hcs24 mRNA was not affected by the same concentration of dexamethasone, which was indicated by the results of an mRNA degradation assay. However, unexpectedly, the prototypic ctgf/hcs24 promoter was not responsible for the dexamethasone stimulation, suggesting the glucocorticoid receptor binding site(s) to be elsewhere in the CTGF/Hcs24 gene. Enhancement of the prototypic promoter activity by dexamethasone was observed in murine fibroblastic cells, demonstrating the complexity of the regulatory mechanism of ctgf/hcs24 gene expression. Of importance, dexamethasone at the same concentration significantly stimulated proteoglycan synthesis in HCS-2/8 cells up to the same levels as exogenously added CTGF/Hcs24. These findings represent a novel effect of glucocorticoid on the production of CTGF/Hcs24 by chondrocytic cells, and indicate that CTGF/Hcs24 may mediate the stimulative effect of dexamethasone on chondrocytic phenotypes. Also, our results shed light on the complex mechanism of CTGF/Hcs24 induction by glucocorticoids.
AB - Connective tissue growth factor (CTGF/Hcs24) is a critical growth factor for chondrocytic growth and differentiation. In this report, we describe for the first time glucocorticoid-mediated induction of the CTGF/Hcs24 gene in a chondrocytic cell line, HCS-2/8. Steady-state mRNA levels of CTGF/Hcs24 were remarkably increased after treatment with 50 nM dexamethasone, as confirmed by Northern blotting and quantitative real-time polymerase chain reaction (PCR) analysis. Corresponding to the increase in mRNA, production of CTGF/Hcs24 protein was remarkably enhanced, following a time course of up to 6 h. The observed increase in mRNA can be ascribed to transcriptional enhancement, since the stability of CTGF/Hcs24 mRNA was not affected by the same concentration of dexamethasone, which was indicated by the results of an mRNA degradation assay. However, unexpectedly, the prototypic ctgf/hcs24 promoter was not responsible for the dexamethasone stimulation, suggesting the glucocorticoid receptor binding site(s) to be elsewhere in the CTGF/Hcs24 gene. Enhancement of the prototypic promoter activity by dexamethasone was observed in murine fibroblastic cells, demonstrating the complexity of the regulatory mechanism of ctgf/hcs24 gene expression. Of importance, dexamethasone at the same concentration significantly stimulated proteoglycan synthesis in HCS-2/8 cells up to the same levels as exogenously added CTGF/Hcs24. These findings represent a novel effect of glucocorticoid on the production of CTGF/Hcs24 by chondrocytic cells, and indicate that CTGF/Hcs24 may mediate the stimulative effect of dexamethasone on chondrocytic phenotypes. Also, our results shed light on the complex mechanism of CTGF/Hcs24 induction by glucocorticoids.
KW - CTGF
KW - Cartilage
KW - Chondrocyte
KW - Connective tissue growth factor
KW - Dexamethasone
KW - HCS-2/8
UR - http://www.scopus.com/inward/record.url?scp=0141527497&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0141527497&partnerID=8YFLogxK
U2 - 10.1016/S8756-3282(03)00227-8
DO - 10.1016/S8756-3282(03)00227-8
M3 - Article
C2 - 14555275
AN - SCOPUS:0141527497
SN - 8756-3282
VL - 33
SP - 694
EP - 702
JO - Bone
JF - Bone
IS - 4
ER -