Abstract
Keratin intermediate filaments are the principal structural element of epithelial cells. Their importance in providing bulk cellular stiffness is well recognized, but their role in the mechanics of cell cortex is less understood. In this study, we therefore compared the cortical stiffness of three keratinocyte lines: primary wild type cells (NHEK2), immortalized wild type cells (NEB1) and immortalized mutant cells (KEB7). The cortical stiffness was measured by lateral indentation of cells with AOD-steered optical tweezers without employing any moving mechanical elements. The method was validated on fixed cells and Cytochalasin-D treated cells to ensure that the observed variations in stiffness within a single cell line were not a consequence of low measurement precision. The measurements of the cortical stiffness showed that primary wild type cells were significantly stiffer than immortalized wild type cells, which was also detected in previous studies of bulk elasticity. In addition, a small difference between the mutant and the wild type cells was detected, showing that mutation of keratin impacts also the cell cortex. Thus, our results indicate that the role of keratins in cortical stiffness is not negligible and call for further investigation of the mechanical interactions between keratins and elements of the cell cortex.
Highlights
Mechanical stiffness of animal cells is provided by the cytoskeleton composed of three main structural elements: actin filaments (AF), microtubules (MT) and intermediate filaments (IF) [1]
Data for vimentin IFs indicated that its disruption influences primarily the stiffness of the cell interior but not the stiffness of the cell cortex [11], and that the measured cell stiffness depends on the indentation depth [25]
Atomic force microscopy (AFM) studies on keratinocytes showed that keratin disruption has a significant impact on cell stiffness under large deformations [12, 13, 21], but the role of keratin at small deformations that penetrate only a few hundreds of nanometers into the cell remained unexplored
Summary
Mechanical stiffness of animal cells is provided by the cytoskeleton composed of three main structural elements: actin filaments (AF), microtubules (MT) and intermediate filaments (IF) [1]. All three filament systems are intertwined and have a large number of associated proteins that interact or bind to them (e.g., motor proteins, focal adhesion proteins, desmosome and hemidesmosome proteins, tight junction proteins, etc.) [3, 4]. In such a complex structure, a disruption of one type of filaments can cause rearrangement of the others [5], and in vivo this can lead to diseases. The important role of IF can be witnessed in karatinocytes
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