©The Author(s) 2025.
World J Stem Cells. Oct 26, 2025; 17(10): 109369
Published online Oct 26, 2025. doi: 10.4252/wjsc.v17.i10.109369
Published online Oct 26, 2025. doi: 10.4252/wjsc.v17.i10.109369
Figure 11 Impact of phosphatase and tensin homolog-induced putative kinase 1 knockdown on GrpE-like 1-mediated changes in interleukin-1 beta-induced CHON-001 cells.
A: Cell viability assessment across experimental groups, evaluating cellular metabolic activity using the CCK-8 assay; B: Transwell migration assay to determine cellular migratory capacity under different conditions (scale bar: 50 μm); C: Western blot analysis of cartilage-associated proteins (collagen II, aggrecan, a disintegrin and metalloproteinase with thrombospondin motifs 5, matrix metalloproteinase-13) to assess matrix metabolism and chondrocyte phenotype. bP < 0.01 vs control; dP < 0.01 vs IL-1β + oeNC + shNC; fP < 0.01 vs IL-1β + GRPEL1 + shNC. OD: Optical density; ADAMTS5: A disintegrin and metalloproteinase with thrombospondin motifs 5; MMP-13: Matrix metalloproteinase-13.
- Citation: Xiang CH, Zou L, Huang ZG, Zhang GJ, Zeng HL, He ZX, Dai ZS. Synovial mesenchymal stem cell-derived exosomes delivering GRPEL1 activate PINK1-mediated mitophagy to promote cartilage repair in arthritis. World J Stem Cells 2025; 17(10): 109369
- URL: https://www.wjgnet.com/1948-0210/full/v17/i10/109369.htm
- DOI: https://dx.doi.org/10.4252/wjsc.v17.i10.109369