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This schematic
shows how we get inject the beads
into cells. We use special needles with an opening only 500nm in diameter. We
inject a red dye along with the beads so that we can identify injected cells
and be sure that the beads are truly within the
cytoplasm of the cell. This work is being done in collaboration with Don Ingber’s group at the |
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At the top left is a phase
contrast image of an endothelial cell that has been microinjected. At the top
right is a fluorescence image showing more than ten beads have been injected
into the cell. Note that the beads are dispersed throughout the cell and do
not aggregate. |
Above is a plot of the mean
squared displacement of injected beads vs. time. Because the cell is a viscoelastic material and not just a simple viscous
liquid the slope of this curve is less than one. The cell is not just a bag
full of liquid – it’s a complex material! |
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In this movie we can see that some beads move much more than others. The beads that move a lot may be within watery micro-compartments of the cell. It appears that some cell types have more of these compartments than others – we are just beginning to sort this out! |
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At the right is a fibroblast
cell that has been injected with 100nm green beads and then fixed and
stained. The red is the filamentous actin structure
within the cell – this biopolymer is very important in giving the cell its
shape, exerting forces on neighboring cells, and regulating biochemical
reactions. The actin structures provide the
stiffness that the cell needs to function within the tissue. The blue is a dye
that binds to DNA and therefore shows the cell’s nucleus. |
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Also, check out our new Cell
Culture Microscope Facility.
Other people who have worked on this project in the past: Andreas Bausch, Hallam Stevens, and Heather Rose.
This page is maintained by:
Cliff Brangwynne
Division of Engineering and
9 &
617-496-9562
brangwyn@fas.harvard.edu