The mechanical properties
of the cell play an important role in essential cellular functions
including mechanotransduction, shape stability, adhesion, motility
and gene expression. Knowledge of cell mechanics is of particular
interest in lung cells given that these cells are continuously subjected
to large cyclic forces owing to breathing. Nanotechnology enables
manipulation of matter with nanometric and picoNewton precision, providing
innovative approaches for studying the structure and function of single
biomolecules and cells under physiological conditions. We use atomic
force microscopy (AFM) and magnetic microbeads (MM) to study the mechanical
properties of lung epithelial cells.
Atomic Force Microscopy
The AFM probe the sample with a sharp
tip (radius of curvature ~ 30 nm) placed at the end of a flexible
cantilever. A piezoelectric actuator drives 3D displacement of the
probe with nanometric precision. The force applied by the tip to the
sample is measured with a laser beam, which is focused at the end
of the cantilever and reflected off onto a segmented photodetector.
High-resolution images under physiological conditions can by obtained
by scanning the surface of the sample keeping the tip-sample force
constant. Mechanical properties of single biomolecules and cells can
be probed by pressing or pulling the sample with the tip and measuring
the force-displacement relationship. Ligand-receptor adhesion can
be probed by coating tip with ligands to cell membrane receptors.
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Atomic Force Microscope (AFM)
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Triangular AFM cantilever. SEM image. The arrow
indicates the tip. The bar is 20 µm.
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| AFM image of human bronchial
epithelial cells (BEAS-2B) in culture. The bar indicates ~10 µm |
Alveolar epithelial cells
(A549) in culture probed with a triangular AFM cantilever. Bright
field image obtained with an inverted microscope. C: triangular
cantilever; T: cantilever tip L: laser beam focused onto the cantilever. |
Magnetic Microbeads
Magnetic microbeads enable sample manipulation
by means of external magnetic fields. Ferromagnetic microbeads (diameter
~ 5 µm) coated with ligands to membrane receptors are attached
to the cell surface. The cell culture is placed on an inverted microscope
and the beads are magnetized in the horizontal plane with a brief
(~1 ms) and large (~100 mT) magnetic pulse. Subsequently, the beads
are subjected to controlled forces and torques by means of magnetic
fields and gradients produced with coils. The movement induced in
the beads is tracked with nanometric resolution by signal processing
of their image recorded with a CCD camera. The relationship between
the magnetic force applied to the beads and the resulting movement
allows us to characterize the mechanical properties of the cytoskeleton
and to identify pathways of force transmission through the cell membrane.
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Magnetic microbeads (arrows) coated with RGD (Arg-Gly-Asp)
containing peptide attached to the surface of bronchial human
epithelial cells (BEAS-2B). Image obtained by scanning electronic
microscopy. The bar indicates 5 µm.
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Contrast phase image of bronchial epithelial cells
(BEAS-2B) in culture with coated ferromagnetic microbeads (dark
dots) attached to the cell membrane.
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| Digitized image of a microbead
recorded with a CCD camera (left). Intensity distribution of the
microbead image (right). |
Related links
Magnetic
Twisting Cytometry
http://www.nature.com/physics/highlights/6853-4.html
-- Physics in biology: soft cells. Nature magazine; Physics Portal,
September, 2001.
http://focus.aps.org/v8/st16.html
-- A cellular glass menagerie, Geoff Brumfiel, Physical Review Focus,
American Physical Society, 24 September, 2001.