Cell intrinsic motility and morphology are highly affected by its surrounding environmental condi... more Cell intrinsic motility and morphology are highly affected by its surrounding environmental conditions. Extracellular proteins have been thoroughly studied along with their effects on Rho GTPases, which been closely linked with cellular movement. Therefore, we investigated the contributing effects two ECM proteins, fibronectin and collagen, have on NIH-3T3 fibroblast motility. In this study, cell motility is characterized through a novel biophysical assay that uses the correlations of the cellular and nuclear centroid minutely displacements to precisely explain the subcellular activity of 3T3 fibroblasts on ECM and also quantify their migration capacity. The results suggest that a fibronectin-rich environment positively affects effective cell displacement and migration potential, compared to a collagen substrate which induced stagnant behavior associated with loss of cell polarity and increased cell sampling, or membrane ruffling. The student t-test was applied to indicate the statistical difference (p < 0.001). This provides us with an insight of the ECM effects on subcellular activity and on the cell-ECM interaction in general. Knowledge gained from these experiments could prove useful in cancer prognosis, diagnosis, or treatment.
Cell intrinsic motility and morphology are highly affected by its surrounding environmental condi... more Cell intrinsic motility and morphology are highly affected by its surrounding environmental conditions. Extracellular proteins have been thoroughly studied along with their effects on Rho GTPases, which been closely linked with cellular movement. Therefore, we investigated the contributing effects two ECM proteins, fibronectin and collagen, have on NIH-3T3 fibroblast motility. In this study, cell motility is characterized through a novel biophysical assay that uses the correlations of the cellular and nuclear centroid minutely displacements to precisely explain the subcellular activity of 3T3 fibroblasts on ECM and also quantify their migration capacity. The results suggest that a fibronectin-rich environment positively affects effective cell displacement and migration potential, compared to a collagen substrate which induced stagnant behavior associated with loss of cell polarity and increased cell sampling, or membrane ruffling. The student t-test was applied to indicate the statistical difference (p < 0.001). This provides us with an insight of the ECM effects on subcellular activity and on the cell-ECM interaction in general. Knowledge gained from these experiments could prove useful in cancer prognosis, diagnosis, or treatment.
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