TY - JOUR
T1 - Expression of c-fos gene inhibits proteoglycan synthesis in transfected chondrocyte
AU - Tsuji, Michiko
AU - Funahashi, Shin Ichi
AU - Takigawa, Masaharu
AU - Seiki, Motoharu
AU - Fujii, Katsuyuki
AU - Yoshida, Takeshi
N1 - Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 1996/3/4
Y1 - 1996/3/4
N2 - The effect of expression of c-fos gene on proteoglycan synthesis, one of the important markers of cartilage metabolism, was examined by introducing the c-fos DNA into HCS 2/8 chondrocytes. The [35S]sulfate incorporation into proteoglycan was decreased in the c-fos transfectants expressing exogenous c-fos mRNA, when compared to a control transfectant. A significant increase in transcription of MMP-3 with the suppressed transcription of aggrecan and TIMP-1 were also observed in the c-fos transfectants. Moreover, analysis of the effect of AP-1 proteins on the collagenase and TIMP-1 promoters in gastric carcinoma KKLS cells revealed that c-Fos combined with any of the Jun-related proteins failed to stimulate the TIMP-1 promoter, though collagenase promoter was effectively activated by any Fos/Jun-related protein heterocomplex. These findings indicate that the c-fos expression may govern the cartilage metabolism and hence may play an important role in the pathogenesis of joint destruction in arthritis.
AB - The effect of expression of c-fos gene on proteoglycan synthesis, one of the important markers of cartilage metabolism, was examined by introducing the c-fos DNA into HCS 2/8 chondrocytes. The [35S]sulfate incorporation into proteoglycan was decreased in the c-fos transfectants expressing exogenous c-fos mRNA, when compared to a control transfectant. A significant increase in transcription of MMP-3 with the suppressed transcription of aggrecan and TIMP-1 were also observed in the c-fos transfectants. Moreover, analysis of the effect of AP-1 proteins on the collagenase and TIMP-1 promoters in gastric carcinoma KKLS cells revealed that c-Fos combined with any of the Jun-related proteins failed to stimulate the TIMP-1 promoter, though collagenase promoter was effectively activated by any Fos/Jun-related protein heterocomplex. These findings indicate that the c-fos expression may govern the cartilage metabolism and hence may play an important role in the pathogenesis of joint destruction in arthritis.
KW - Activating protein-1
KW - Chondrocyte
KW - Matrix metalloproteinase-3
KW - Proteoglycan
KW - Tissue inhibitor of metalloproteinase-1
KW - c-fos
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U2 - 10.1016/0014-5793(96)00118-4
DO - 10.1016/0014-5793(96)00118-4
M3 - Article
C2 - 8601460
AN - SCOPUS:0029925577
SN - 0014-5793
VL - 381
SP - 222
EP - 226
JO - FEBS Letters
JF - FEBS Letters
IS - 3
ER -