Optimal characterization of the mechanical properties of both cells and their
surrounding is an issue of major interest. Indeed, cell function and
development are strongly influenced by external stimuli. Furthermore, a change
in cell mechanics might, in some cases, associate with diseases or
malfunctioning. In this work, atomic force microscopy (AFM) was applied to
examine the mechanical properties of the silicone elastomer
polydimethylsiloxane (PDMS) a common substrate in cell culture. Force
spectroscopy analysis was done over different specimens of this elastomeric
material containing varying ratios of resin to cross-linker in its structure
(5:1, 10:1, 20:1, 30:1 and 50:1), which impacts the final material properties
(e.g., stiffness, elasticity). To quantify the mechanical properties of the
PDMS, factors as the modulus of Young, the maximum adhesive forces as well as
both relaxation amplitudes and times upon constant height contact of the tip
(dwell time different of zero) were calculated from the different segments
forming the force curves. It is demonstrated that the material stiffness is
increased by prior oxygen plasma treatment of the sample, required for
hydrophilic switching, contrarily to what observed for its adhesiveness.
Subsequent incubation of endothelial HUVEC cells on top of these plasma treated
PDMS systems yields minor variation in cell mechanics in comparison to those
obtained on a glass reference, on which cells show much higher spreading
tendency and, by extension, a remarkable membrane hardening. Thus, surface
wettability turns a factor of higher relevance than substrate stiffness
inducing variations in the cell mechanics.Comment: manuscript (12 pages, 4 figures, 2 tables), supplementary information
(2 pages and 3 figures), the main results of the manuscript are based on a
master thesi