Comparing the mechanical influence of vinculin, focal adhesion kinase and p53 in mouse embryonic fibroblasts |
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Authors: | Anna H Klemm Josè-Luis Alonso |
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Institution: | a Center for Medical Physics and Technology, Biophysics Group, Friedrich-Alexander-University of Erlangen-Nuremberg, 91052 Erlangen, Germany b Massachusetts General Hospital/Harvard Medical School, Charlestown, MA 02129, USA |
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Abstract: | Cytoskeletal reorganization is an ongoing process when cells adhere, move or invade extracellular substrates. The cellular force generation and transmission are determined by the intactness of the actomyosin-(focal adhesion complex)-integrin connection. We investigated the intracellular course of action in mouse embryonic fibroblasts deficient in the focal adhesion proteins vinculin and focal adhesion kinase (FAK) and the nuclear matrix protein p53 using magnetic tweezer and nanoparticle tracking techniques. Results show that the lack of these proteins decrease cellular stiffness and affect cell rheological behavior. The decrease in cellular binding strength was higher in FAK- to vinculin-deficient cells, whilst p53-deficient cells showed no effect compared to wildtype cells. The intracellular cytoskeletal activity was lowest in wildtype cells, but increased in the following order when cells lacked FAK+p53 > p53 > vinculin. In summary, cell mechanical processes are differently affected by the focal adhesion proteins vinculin and FAK than by the nuclear matrix protein, p53. |
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Keywords: | Mouse embryonic fibroblasts Vinculin Focal adhesion kinase p53 Cell stiffness Binding strength Diffusivity |
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