摘要：SummaryOsteoarthritis (OA) is the most prevalent chronic joint disease that affects a large proportion of the elderly population. Chondrogenic progenitor cells (CPCs) reside in late-stage OA cartilage tissue, producing a fibrocartilaginous extracellular matrix; these cells can be manipulatedin vitroto deposit proteins of healthy articular cartilage.CPCs are under the control of SOX9 and RUNX2. In our earlier studies, we showed that a knockdown of RUNX2 enhanced the chondrogenic potential of CPCs. Here we demonstrate that CPCs carrying a knockout of RAB5C, a protein involved in endosomal trafficking, exhibited elevated expression of multiple chondrogenic markers, including the SOX trio, and increased COL2 deposition, whereas no changes in COL1 deposition were observed.We report RAB5C as an attractive target for future therapeutic approaches designed to increase the COL2 content in the diseased joint.Graphical abstractDisplay OmittedHighlights•RUNX2 has a pro-chondrogenic effect in CPCs.•RAB5C is a potential interaction partner of SOX9 in CPCs.•Loss of RAB5C increases the chondrogenic potential of CPCs.Stem cells research; Omics; Proteomics ; Transcriptomics
