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©The Author(s) 2024.
World J Stem Cells. Nov 26, 2024; 16(11): 926-943
Published online Nov 26, 2024. doi: 10.4252/wjsc.v16.i11.926
Published online Nov 26, 2024. doi: 10.4252/wjsc.v16.i11.926
Figure 3 Hydrogen peroxide inhibited stemness and promoted senescence in periodontal ligament stem cells.
A: Hydrogen peroxide (H2O2) inhibited the expression level of stemness-related proteins C-MYC, OCT-4, and NANOG in periodontal ligament stem cells (PDLSCs); B: H2O2 suppressed the expression levels of stemness-related genes C-MYC, OCT-4, and NANOG in PDLSCs; C: Alkaline phosphatase staining and alkaline phosphatase activity showed that the osteogenic differentiation ability of the H2O2-induced PDLSCs was weaker than that of the control group; D: Alizarin Red staining and quantitative analysis showed that the osteogenic differentiation ability of the H2O2-induced PDLSCs was weaker than that of the control group; E: Senescence-associated β-galactosidase staining indicated significantly more senescence-associated β-galactosidase-positive cells in H2O2-induced PDLSCs compared with the control group; F: Western blot results showed that H2O2 inhibited the expression of p-RB but increased the expression of p21 in PDLSCs. Data are presented as mean ± SD, n = 3. aP < 0.05; bP < 0.01; cP < 0.001; dP < 0.0001. NC: Negative control; H2O2: Hydrogen peroxide; ALP: Alkaline phosphatase; SA β-gal: Senescence-associated β-galactosidase.
- Citation: Gu K, Feng XM, Sun SQ, Hao XY, Wen Y. Yes-associated protein-mediated melatonin regulates the function of periodontal ligament stem cells under oxidative stress conditions. World J Stem Cells 2024; 16(11): 926-943
- URL: https://www.wjgnet.com/1948-0210/full/v16/i11/926.htm
- DOI: https://dx.doi.org/10.4252/wjsc.v16.i11.926