bioRxivBiophysics
Keratins determine network stress responsiveness in reconstituted actin-keratin filament systems
I. Elbalasy, P. Mollenkopf, C. Tutmarc, H. Herrmann, J. Schnauss
Abstract
The cytoskeleton is a major determinant of cell mechanics, a property that is altered during many pathological situations. To understand these alterations, it is essential to investigate the interplay between the main filament systems of the cytoskeleton in the form of composite networks. Here, we investigate the role of keratin intermediate filaments (IFs) in network strength by studying in vitro reconstituted actin and keratin 8/18 composite networks via bulk shear rheology. We co-polymerized these structural proteins in varying ratios and recorded how their relative content affects the overall mechanical response of the various composites. For relatively small deformations, we found that all composites exhibited an intermediate linear viscoelastic behavior compared to that of the pure networks. In stark contrast, the composites displayed increasing strain stiffening behavior as a result of increased keratin content when larger deformations were imposed. This strain stiffening behavior is fundamentally different from behavior encountered with vimentin IF as a composite network partner for actin. Our results provide new insights into the mechanical interplay between actin and keratin in which keratin provides reinforcement to actin. This interplay may contribute to the overall integrity of cells, providing an explanation for the stability of stressed epithelial tissues due to their high keratin contents. Additionally, this helps us to understand the physiological necessity to exchange IF systems during epithelial-mesenchymal transition (EMT) in order to suppress strain stiffening of the network, making cells more elastic and, thus, facilitating their migration through dense tissues.
- research focus: cell signaling & trafficking
- research focus: metabolism & bioenergetics
- research focus: development & morphogenesis
- research focus: cell type annotation
- approach: experimental assay
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