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. 2013 Aug 2;20(10):1393–1403. doi: 10.1038/cdd.2013.93

Figure 7.

Figure 7

Knockdown of Bim protects cells from apoptosis induced by Aurora A inhibition. (a) Bim expression was knocked down in HeLa cells using two different lentivirus delivered shRNAs (sh-Bim1 and shBim2). A non-silencing shRNA (sh-NS) was used as control. (Top) Knockdown and control cells were treated with 5 μM MLN8054 for 72 h. Resulting tissue culture plates were stained with crystal violet. (Bottom) Immunoblots of whole-cell extracts confirming knockdown in Bim shRNA-expressing cells. β-Actin is shown as loading control. (b) Quantitation of cell numbers from experiment in a. Student's t-test was used to determine statistical significance (*P≤0.05, **P≤0.01). (c) Control (sh-NS) or sh-Bim1 and sh-Bim2 HeLa cells were treated with 5 μM MLN8054 for 48 h. Immunoblots of whole-cell extracts were performed to confirm Bim knockdown and cleaved PARP-1 and Caspase 3 were used to demonstrate apoptotic effect of MLN8054. β-Actin is shown as a loading control. (d) HeLa cells were treated as described for c, stained with AnnexinV and 7AAD, and analyzed by flow cytometry. The percentage of AnnexinV-positive cells is indicated for each treatment. Grey bars indicate untreated and black bars are treatment with MLN8054