| Literature DB >> 29402405 |
Wataru Korogi1, Tatsuya Yoshizawa2, Md Fazlul Karim3, Hironori Tanoue4, Masaki Yugami4, Shihab U Sobuz3, Eiichi Hinoi5, Yoshifumi Sato3, Yuichi Oike4, Hiroshi Mizuta6, Kazuya Yamagata3.
Abstract
Sirtuins (SIRT1-7) are NAD+-dependent deacetylase/deacylases that regulate a wide variety of biological functions. Although the roles of sirtuins in cartilage homeostasis and cartilage diseases have been well studied, there is no information on the contribution of SIRT7 to cartilage homeostasis and osteoarthritis (OA) pathologies. Here, we demonstrate that Sirt7 knockout mice are resistant to the development of aging-associated OA and forced exercise-induced OA. Attenuation of Sirt7 in the murine chondrogenic cell line ATDC5 increased the deposition of a glycosaminoglycan-rich extracellular matrix and the mRNA expression of extracellular matrix components such as Col2a1 and Acan. Mechanistically, we found that SIRT7 suppressed the transcriptional activity of SOX9, which is an important transcription factor in chondrocytes, and that the enzymatic activity of SIRT7 was required for its function. Our results indicate that SIRT7 is a novel important regulator of cartilage homeostasis and OA development.Entities:
Keywords: Chondrocyte; Deacylase; Osteoarthritis; SIRT7; SOX9; Sirtuin
Year: 2018 PMID: 29402405 DOI: 10.1016/j.bbrc.2018.01.129
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575