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. 2021 Feb 22;12:1213. doi: 10.1038/s41467-021-21447-2

Fig. 8. KIF18A KD-induced defects depend on dynamic microtubules and are enhanced by increased KIF2C/MCAK activity.

Fig. 8

a Representative images (from three independent experiments) of MDA-MB-231 cell density 96 h after the start of high-contrast bright-field imaging. Cells were treated with either control or KIF18A siRNAs in combination with DMSO or 500 nM UMK57. Scale bar is 100 microns. b Fold change in cell density after 96 h in MDA-MB-231 cells treated with the specified siRNAs and either 500 nM UMK57 or DMSO. n = 76 (control KD + DMSO), 52 (control KD + UMK57), 76 (KIF18A KD + DMSO), and 68 (KIF18A KD + UMK57) wells of cells from three independent experiments. Data were analyzed via one-way ANOVA with post hoc Tukey’s test for multiple comparisons. c, d Percent of total mitotic cells (c) and mitotic cells with multipolar spindles (d) in fixed populations after the indicated treatments. n = 3 independent experimental replicates per condition. Data were analyzed via one-way ANOVA with post hoc Tukey’s test for multiple comparisons. e, f Percent of live, siR-tubulin-labeled MDA-MB-231 cells that (e) split poles or (f) entered mitosis with more than two spindle poles after the indicated treatments. n = 126 (control KD + DMSO), 158 (control KD + UMK57), 172 (KIF18A KD + DMSO), and 152 (KIF18A KD + UMK57) mitotic cells from three independent experiments. Data were analyzed via a two-sided Chi-square test. All graphs show mean ± SD and individual data points. P values <0.05 are displayed.