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. Author manuscript; available in PMC: 2010 Aug 6.
Published in final edited form as: Acta Biomater. 2007 May 30;3(4):413–438. doi: 10.1016/j.actbio.2007.04.002

Fig. 19.

Fig. 19

Effects of cell type, chemotherapy exposure time and cell death on the stiffness of leukemia cells. (Top figure) The red line and associated data points show that isolated HL60 cells exposed to 1 µM daunorubicin at time 0 (vertical dashed green line) exhibit increased stiffness (by a factor of more than 30) as a function of time of exposure to this chemotherapy agent. If these cells are now also simultaneously treated with 2 µM cytochalasin D, an actin polymerization inhibitor, at time 0, almost no increase in stiffness is seen (green line and data points) with chemotherapy exposure time and cell death. If the cells are simultaneously treated with 2 µM cytochalasin D, at time t = 45 min (indicated by the vertical dashed blue line) after the 1 µM daunorubicin treatment commences, no further increase (in fact a slight reduction) in stiffness is seen (blue line and data points) with chemotherapy exposure time and cell death. (Lower left figure) The average stiffness of dead cells (beige bars) for both HL60 and Jurkat cell lines exposed to both daunorubicin and cytochalasin D is much lower than that for the same cells exposed only to daunorubicin (red bars). (Bottom right figure) The stiffness of isolated AML cells increases as cell death progresses upon treatment with 1 µM daunorubicin. Results adapted from Ref. [133].