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. 2022 Nov 10;54(11):1927–1939. doi: 10.1038/s12276-022-00879-w

Fig. 1. Phenotypic characterization of primary articular chondrocytes and the cytotoxicity of SA on chondrocytes.

Fig. 1

a Staining of articular chondrocytes in primary cultures with toluidine blue. Immunostaining of primary articular chondrocytes with Col2a1 (red), ACAN (green) and DAPI (blue). b Flow cytometry for cell cycle progression of chondrocytes with or without SA (i). Quantitative analysis (ii) found that SA significantly promoted S-phase cells (n = 3, Student’s t test). c Chondrocytes were treated with SA at gradient concentrations (0-100 μM) for 48 h and subjected to CCK-8 analysis. From 5 μM to 20 μM SA treatment, the OD values were significantly higher than those of the 0 μM (DMSO) group, and for 50 μM and 100 μM SA treatment, the OD values were significantly lower than those of the 0 μM (DMSO) group (n = 5, one-way ANOVA). d Chondrocyte proliferation curve with SA treatment from Day 1 to Day 5. Compared with DMSO treatment, 10 μM SA treatment significantly promoted cell proliferation from Day 1 to Day 5 (n = 5, Student’s t test). e IC50 of SA on chondrocytes; concentrations were transferred to Log(c). The data are expressed as the mean ± SD, *p < 0.05, **p < 0.01, ***p < 0.001, *compared with the DMSO group, #p < 0.05, ##p < 0.01, ###p < 0.001, # compared with the indicated group.