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. 2021 Mar 8;129(3):037002. doi: 10.1289/EHP7102

Figure 4.

Figures 4A and 4C are staining of Michigan Cancer Foundation-7 cells and methylenedioxyamphetamine-M B-231 cells following exposure to 2,3,7,8-Tetrachlorodibenzo-italic p-dioxin, co-culture or coexposure with scale bar of 20 micrometers displaying three columns, namely, Actin, Paxillin, and Merge and four rows, namely, control, 2,3,7,8-Tetrachlorodibenzo-italic p-dioxin, Co-culture, and Coexposure. Figure 4B is a set of two bar graphs titled Cell number per field and Giant cells per field plotting Quantitation, ranging from 0 to 150 in increments of 50 and 0 to 5 in unit increments (y-axis) across control, 2,3,7,8-Tetrachlorodibenzo-italic p-dioxin, Co-culture, and Coexposure (x-axis), respectively.

Morphological differences of MCF7 cells and MDA-MB-231 cells following exposure to TCDD, co-culture, or coexposure. Cells were grown with hMADS and/or treated with 25 nM TCDD [Control (vehicle MCF-7 cells, alone), TCDD (MCF-7 cells treated with 25nM TCDD), co-culture (MCF-7 co-cultured with hMADS), and coexposure (co-culture with TCDD)]. After 48 h treatment, cells were fixed and stained for paxillin, actin, and nucleus (blue). (A) Staining of MCF7 cells. Scale bar 20μm. (B) Quantitation of MCF7 cell number and giant cells (very large cells with multiple nuclei) per field (n=3) field per conditions. Graph represents means±SEM of three experiments. The numerical information mean±SEM and p-values are provided in Table S4. Kruskal–Wallis’s H test (nonparametric comparison of k independent series) followed by a 1-factor ANOVA test (parametric comparison of k independent series, *p<0.05). (C) Staining of MDA-MB-231. Scale bar 20μm. Symbols were used to point out the focal adhesions (arrow), lamellipods (*) and giant cells (#). Note: ANOVA, analysis of variance; SEM, standard error of the mean; TCDD, 2,3,7,8-tetrachlorodibenzo-p-dioxin.