Abstract

Loading frequency is known to influence the expression of the focal adhesions of the adherent cells. A small cyclical tensile force was transmitted to mouse pre-osteoblast MC3T3-E1 cells through PDMS substrates of varying stiffness. Changes in cell behavior with respect to proliferation and characteristics of focal adhesions were quantified through immunofluorescence labeling of vinculin. Amount of inactive vinculin was higher on substrates subjected to cyclic stimulation when compared with the results of the static substrates, whereas the number and area of focal adhesion points underwent a reduction. Inactive vinculin appears as a cloud in the cytoplasm in the vicinity of the nucleus.

Highlights

  • Value of the dataVinculin expression appears to increase under cyclic stimulus Fewer and smaller focal adhesion points for cyclic stimulus vis-à-vis static loading of substrate Vinculin appears as a cloud in the cytoplasm in the vicinity of the nucleus

  • Loading frequency is known to influence the expression of the focal adhesions of the adherent cells

  • A small cyclical tensile force was transmitted to mouse pre-osteoblast MC3T3-E1 cells through PDMS substrates of varying stiffness

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Summary

Value of the data

Vinculin expression appears to increase under cyclic stimulus Fewer and smaller focal adhesion points for cyclic stimulus vis-à-vis static loading of substrate Vinculin appears as a cloud in the cytoplasm in the vicinity of the nucleus. The characteristics of vinculin expression at focal adhesion points and in the cytoplasm are described through the use of a table and confocal microscope images

Cell line
Fibronectin coating
Mechanical stimulation
Immunofluorescence labeling
Substrate stiffness
Image processing: focal adhesions and vinculin
Statistical analysis
Vinculin immunofluorescence Imaging
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