Cell–material
interactions are crucial for many biomedical
applications, including medical implants, tissue engineering, and
biosensors. For implants, while the adhesion of eukaryotic host cells
is desirable, bacterial adhesion often leads to infections. Surface
free energy (SFE) is an important parameter that controls short- and
long-term eukaryotic and prokaryotic cell adhesion. Understanding
its effect at a fundamental level is essential for designing materials
that minimize bacterial adhesion. Most cell adhesion studies for implants
have focused on correlating surface wettability with mammalian cell
adhesion and are restricted to short-term time scales. In this work,
we used quartz crystal microbalance with dissipation monitoring (QCM-D)
and electrical impedance analysis to characterize the adhesion and
detachment of S. cerevisiae and E. coli, serving as model eukaryotic and prokaryotic cells within extended
time scales. Measurements were performed on surfaces displaying different
surface energies (Au, SiO2, and silanized SiO2). Our results demonstrate that tuning the surface free energy of
materials is a useful strategy for selectively promoting eukaryotic
cell adhesion and preventing bacterial adhesion. Specifically, we
show that under flow and steady-state conditions and within time scales
up to ∼10 h, a high SFE, especially its polar component, enhances S. cerevisiae adhesion and hinders E. coli adhesion. In the long term, however, both cells tend to detach,
but less detachment occurs on surfaces with a high dispersive SFE
contribution. The conclusions on S. cerevisiae are
also valid for a second eukaryotic cell type, being the human embryonic
kidney (HEK) cells on which we performed the same analysis for comparison.
Furthermore, each cell adhesion phase is associated with unique cytoskeletal
viscoelastic states, which are cell-type-specific and surface free
energy-dependent and provide insights into the underlying adhesion
mechanisms.