Research Paper Volume 14, Issue 15 pp 6128—6148

Figure 8. Dynamic change of Mcl-1 levels in vector-αTN4-1 and MAB21L1-αTN4-1 cells in the absence and presence of 100 OA treatment and effect of Mcl-1 level on OA-induced apoptosis of αTN4-1 cells. (A, B) Dynamic change of Mcl-1 levels in vector-αTN4-1 and MAB21L1-αTN4-1 cells in the absence and presence of 100 OA treatment. Both vector-αTN4-1 and MAB21L1-αTN4-1 cells were grown to about 90% confluence and then subjected to 100 nM OA treatment for 12 and 24 hrs. Thereafter, the cells were harvested for extraction of total proteins which were used for analysis of Mcl-1 expression by Western blot analysis (A). Quantitative results of the Mcl-1 protein expression levels were analyzed by Image J software (B). Note that in the MAB21L1-αTN4-1 cells, the Mcl-1 protein expression level was much lower than that in the vector-αTN4-1 cell clone in the absence of 100 nM OA treatment. During OA treatment for 12 and 24 hrs, however, Mcl-1 protein was down-regulated to background level in vector-αTN4-1 cells. In contrast, in MAB21L1-αTN4-1 cells, Mcl-1 protein was significantly upregulated after 24 h treatment by OA. N=3. ** p<0.01, *** p<0.001. (C, D) Effect of Mcl-1 level on OA-induced apoptosis of αTN4-1 cells. Both pCI-αTN4-1 and pCI-Mcl-1-αTN4-1 cell clones were verified with Western blot analysis (C). The two types of pCI-αTN4-1 and pCI-Mcl-1-αTN4-1 cells were then subjected to 100 nM OA treatment for 12 and 24 hrs, and the apoptosis rate was determined with live/dead assays (D). N=3. *p<0.05, ** p<0.01.