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논문 기본 정보

자료유형
학술저널
저자정보
Riko Nishimura (Osaka University Graduate School of Dentistry) Kenji Hata (Osaka University Graduate School of Dentistry) Yoshifumi Takahata (Osaka University Graduate School of Dentistry) Tomohiko Murakami (Osaka University Graduate School of Dentistry) Eriko Nakamura (Osaka University Graduate School of Dentistry) Hiroko Yagi (Osaka University Graduate School of Dentistry)
저널정보
대한골대사학회 대한골대사학회지 대한골대사학회지 제24권 제3호
발행연도
2017.8
수록면
147 - 153 (7page)
DOI
https://doi.org/10.11005/jbm.2017.24.3.147

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Genetic studies and molecular cloning approaches have been successfully used to identify several transcription factors that regulate the numerous stages of cartilage development. Sex-determining region Y (SRY)-box 9 (Sox9) is an essential transcription factor for the initial stage of cartilage development. Sox5 and Sox6 play an important role in the chondrogenic action of Sox9, presumably by defining its cartilage specificity. Several transcription factors have been identified as transcriptional partners for Sox9 during cartilage development. Runt-related transcription factor 2 (Runx2) and Runx3 are necessary for hypertrophy of chondrocytes. CCAAT/enhancer-binding protein β (C/EBPβ) and activating transcription factor 4 (ATF4) function as co-activators for Runx2 during hypertrophy of chondrocytes. In addition, myocyte-enhancer factor 2C (Mef2C) is required for initiation of chondrocyte hypertrophy, presumably by functioning upstream of Runx2. Importantly, the pathogenic roles of several transcription factors in osteoarthritis have been demonstrated based on the similarity of pathological phenomena seen in osteoarthritis with chondrocyte hypertrophy. We discuss the importance of investigating cellular and molecular properties of articular chondrocytes and degradation mechanisms in osteoarthritis, one of the most common cartilage diseases.

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