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. 2017 Jul 19;40(3):713–720. doi: 10.3892/ijmm.2017.3073

Figure 4.

Figure 4

Proliferation and adipogenesis of ASCs was examined. CCK-8 assay was conducted after the cells were incubated with 1×10−2, 2×10−2, 3×10−2, 4×10−2, 5×10−2, 6×10−2, 7×10−2, 8×10−2 U/ml BoNTA for 5 days (A); the cells were treated with 8×10−2, 1.5×10−1, 2×10−1, 3×10−1, 4×10−1, 5×10−1 U/ml BoNTA for 3 days (B). The control group (C-a and C-c) and BoNTA group (C-b and C-d) were stained with Oil Red O after being induced to differentiate into adipocytes on day 8 (C-a and C-b; scale bar, 2 µm; C c and C d; scale bar, 2 µm). Quantification of Oil Red O staining was assessed by isopropanol leaching and absorbance at 51 nm (D). Data are the means ± standard deviation of 3 separate experiments. *P<0.05, **P<0.01, t-test vs. control (no treatment). ASCs, adipose-derived stem cells; BoNTA, botulinum toxin A.