Kubitschke, Hans
[Author];
Schnauß, Jörg
[Author];
Nnetu, Kenechukwu David
[Author];
Warmt, Enrico
[Author];
Stange, Roland
[Author];
Käs, Josef A.
[Author]
Actin and microtubule networks contribute differently to cell response for small and large strains
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Media type:
E-Article
Title:
Actin and microtubule networks contribute differently to cell response for small and large strains
Contributor:
Kubitschke, Hans
[Author];
Schnauß, Jörg
[Author];
Nnetu, Kenechukwu David
[Author];
Warmt, Enrico
[Author];
Stange, Roland
[Author];
Käs, Josef A.
[Author]
Footnote:
Hinweis: Link zur Erstveröffentlichung URL: https://doi.org/10.1088/1367-2630/aa7658
Description:
Cytoskeletal filaments provide cells with mechanical stability and organization. The main key players
are actin filaments and microtubules governing a cell’s response to mechanical stimuli. We
investigated the specific influences of these crucial components by deforming MCF-7 epithelial cells at
small(5% deformation) and large strains(>5% deformation). To understand specific contributions
of actin filaments and microtubules, we systematically studied cellular responses after treatment with
cytoskeleton influencing drugs. Quantification with the microfluidic optical stretcher allowed
capturing the relative deformation and relaxation of cells under different conditions. We separated
distinctive deformational and relaxational contributions to cell mechanics for actin and microtubule
networks for two orders of magnitude of drug dosages. Disrupting actin filaments via latrunculin A,
for instance, revealed a strain-independent softening. Stabilizing these filaments by treatment with
jasplakinolide yielded cell softening for small strains but showed no significant change at large strains.
In contrast, cells treated with nocodazole to disrupt microtubules displayed a softening at large strains
but remained unchanged at small strains. Stabilizing microtubules within the cells via paclitaxel
revealed no significant changes for deformations at small strains, but concentration-dependent
impact at large strains. This suggests that for suspended cells, the actin cortex is probed at small strains,
while at larger strains; the whole cell is probed with a significant contribution from the microtubules