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Journal of Korean Medical Science ; : 100-106, 2006.
Article in English | WPRIM | ID: wpr-71345

ABSTRACT

The purpose of this study was to demonstrate the cellular localization of cyclooxygenase-2 (COX-2) and caveolin-3 (Cav-3) in primarily cultured rat chondrocytes. In normal rat chondrocytes, we observed relatively high levels of Cav-3 and a very low level of COX-2 mRNA and protein. Upon treating the chondrocytes with 5 microM of CdCl2 (Cd) for 6 hr, the expressions of COX-2 mRNA and protein were increased with the decreased Cav-3 mRNA and protein expressions. The detergent insoluble caveolae-rich membranous fractions that were isolated from the rat chondrocytes and treated with Cd contained the both proteins of both COX-2 and Cav-3 in a same fraction. The immuno-precipitation experiments showed complex formation between the COX-2 and Cav-3 in the rat chondrocytes. Purified COX-2 with glutathione S-transferase-fused COX-2 also showed complex formation with Cav-3. Confocal and electron microscopy also demonstrated the co-localization of COX-2 and Cav-3 in the plasma membrane. The results from our current study show that COX-2 and Cav-3 are co-localized in the caveolae of the plasma membrane, and they form a protein-protein complex. The co-localization of COX-2 with Cav-3 in the caveolae suggests that the caveolins might play an important role for regulating the function of COX-2.


Subject(s)
Animals , Rats , Animals, Newborn , Blotting, Western , Cadmium Chloride/pharmacology , Caveolae/drug effects , Caveolin 3/genetics , Cell Membrane/drug effects , Cells, Cultured , Chondrocytes/cytology , Cyclooxygenase 2/genetics , Gene Expression , Immunoprecipitation , Microscopy, Confocal , Microscopy, Electron , RNA, Messenger/genetics , Reverse Transcriptase Polymerase Chain Reaction
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