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. Author manuscript; available in PMC: 2021 Mar 27.
Published in final edited form as: Cell Rep. 2021 Mar 9;34(10):108816. doi: 10.1016/j.celrep.2021.108816

Figure 4. Tuning contractility modulates adurotaxis in adhesion-sorted cells.

Figure 4.

(A) Model PDF of cell distribution versus simulated hydrogel position as predicted for 30 (purple), 35 (yellow), 40 (red), and 45 pN (blue) max SF forces at t = 0 and t = 24 h. Durotactic tendency increased with decreasing max SF force.

(B) Weakly adherent MDA-MB-231 cell speed on soft or stiff side of step-gradient hydrogels for cells is plotted. Data are shown for blebbistatin-treated and nontreated cells, i.e., DMSO (orange) versus 100 μM (blue), and cells on softer (open) versus stiffer (closed) regions. (n > 245 cells for each condition from triplicate experiments). ***p < 10−3, ****p < 10−4 were determined by one-way ANOVA with Tukey test for multiple comparisons for the indicated comparisons.

(C) For treated and nontreated weakly adherent MDA-MB-231 cells that encounter the step gradient, the fraction of durotactic, anti-durotactic, and adurotactic behavior is plotted. Data represent n = 154 of 256 DMSO-treated and 167 of 245 blebbistatin-treated cells over triplicate experiments; those not counted did not interact with the gradient. Comparisons were made using a Fisher’s exact test for the same migration behavior between treated and DMSO, *p < 0.05.

(D) Weakly adherent MDA-MB-231 PDF of cell distribution was plotted versus hydrogel position for blebbistatin treatment of 100 μM (purple), 10 μM (yellow), 1 μM (red), or DMSO (blue) at t = 3 and t = 27 h.

(E) Strongly adherent MDA-MB-231 PDF of cell distribution was plotted versus hydrogel position for LPA treatment of 10 μM (yellow), 1 μM (red), or DMSO (blue) at t = 3 and t = 24 h.