Ontology highlight
ABSTRACT: Background
Cellular senescence is a critical factor contributing to osteoarthritis (OA). Overexpression of chromobox homolog 4 (CBX4) in a mouse system was demonstrated to alleviate post-traumatic osteoarthritis (PTOA) by reducing cellular senescence. Additionally, replicative cellular senescence of WI-38 fibroblasts can be attenuated by CBX4. However, the mechanisms underlying this senomorphic function of CBX4 are not fully understood. In this study, we aimed to investigate the role of CBX4 in cellular senescence in human primary osteoarthritic chondrocytes and to identify the functional domains of CBX4 necessary for its function in modulating senescence.Methods
Chondrocytes, isolated from 6 individuals undergoing total knee replacement for OA, were transduced with wild-ty
SUBMITTER: Chen YH
PROVIDER: S-EPMC10568837 | biostudies-literature | 2023 Oct
REPOSITORIES: biostudies-literature