MAPK/ERK通路
神经酰胺
细胞生物学
化学
II型胶原
激酶
分子生物学
信号转导
酸性鞘磷脂酶
MEK抑制剂
Ⅰ型胶原
软骨
生物
内分泌学
生物化学
细胞凋亡
解剖
作者
Sophie Gilbert,Emma J. Blain,Victor C. Duance,D.J. Mason
摘要
Abstract Objective Ceramide, a mediator of proinflammatory cytokine signaling, induces cartilage degradation and reduces type II collagen synthesis in articular cartilage. The accumulation of ceramide is associated with arthritis in Farber's disease. The aim of this study was to investigate the mechanism of ceramide‐induced down‐regulation of type II collagen. Methods Bovine articular chondrocytes were stimulated with sphingomyelinase (SMase) to increase levels of endogenous ceramide. Components of the ERK pathway were inhibited by Raf‐1 kinase inhibitor and the MEK inhibitor, PD98059. Cell extracts were analyzed by Western blotting for ERK‐1/2, SOX9, c‐Fos, and type II collagen, and the level of c ‐ fos messenger RNA (mRNA) was analyzed by quantitative polymerase chain reaction. Localization of ERK‐1/2, SOX9, and c‐Fos was assessed by immunocytochemistry and confocal microscopy. Results SMase treatment of chondrocytes caused sustained phosphorylation of ERK‐1/2 throughout the cytoplasm and nucleus that was reduced by inhibitors of Raf‐1 kinase and MEK‐1/2. SMase treatment of chondrocytes also induced translocation of c‐Fos to the nucleus and phospho‐SOX9 to the cytoplasm and increased expression of c ‐ fos mRNA. Type II collagen expression, which was down‐regulated by SMase treatment, was restored by the MEK‐1/2 inhibitor, PD98059. Conclusion SMase down‐regulates type II collagen in articular chondrocytes via activation of the ERK signaling cascade, redistribution of SOX9, and recruitment of c‐Fos. This new mechanism for cartilage degradation provides potential targets for future treatment of arthritic disease.
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