SIRT7 is an important regulator of cartilage homeostasis and osteoarthritis development

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. •Sirt7 knockout mice are resistant to the development of aging-associated osteoarthritis.•Sirt7 knockout mice are resistant to the development of forced exercise-induced osteoarthritis.•Attenuation of SIRT7 in chondrocytes increases the expression of extracellular matrixes.•SIRT7 suppresses transcriptional activity of SOX9 via deacylation activity.•SIRT7 is important for cartilage homeostasis and osteoarthritis development.