Atomic force microscopy (AFM) has been used to study
the mechanical
properties of cells, in particular, malignant cells. Softening of
various cancer cells compared to their nonmalignant counterparts has
been reported for various cell types. However, in most AFM studies,
the pericellular layer was ignored. As was shown, it could substantially
change the measured cell rigidity and miss important information on
the physical properties of the pericellular layer. Here we take into
account the pericellular layer by using the brush model to do the
AFM indentation study of bladder epithelial bladder nonmalignant (HCV29)
and cancerous (TCCSUP) cells. It allows us to measure not only the
quasistatic Young’s modulus of the cell body but also the physical
properties of the pericellular layer (the equilibrium length and grafting
density). We found that the inner pericellular brush was longer for
cancer cells, but its grafting density was similar to that found for
nonmalignant cells. The outer brush was much shorter and less dense
for cancer cells. Furthermore, we demonstrate a method to convert
the obtained physical properties of the pericellular layer into biochemical
language better known to the cell biology community. It is done by
using heparinase I and neuraminidase enzymatic treatments that remove
specific molecular parts of the pericellular layer. The presented
here approach can also be used to decipher the molecular composition
of not only pericellular but also other molecular layers.