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. 2019 Nov 5;116(47):23671–23681. doi: 10.1073/pnas.1910097116

Fig. 5.

Fig. 5.

ER stress alters cell morphology, actin turnover dynamics, and intracellular actin filament organization in THP1 CD1d cells. Cells were treated with appropriate control solvent (DMSO or Glycerol) or ER stress-inducing drugs (thapsigargin 0.03 μM or 1 μg/mL SubAB5). (A and B) microscopic images of actin fluorescence for quantification of actin distribution area. (i) Image of a cell treated with the solvent control; (ii) the corresponding ER-stress condition. (C and D) FRAP analysis of fluorescence recover of control or ER-stressed THP1 cells to measure actin filament polymerization dynamics. Panel (i) shows half-time of fluorescence recovery and (ii) compares the mobile an immobile actin fractions upon treatment. The data represent n ≥ 3 biological replicates. *P < 0.05, **P < 0.005, ****P < 0.0001 by unpaired, 2-tailed t test.