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dc.contributor.authorWang, Hong-Bei
dc.contributor.authorDembo, Micah
dc.contributor.authorHanks, Steven K.
dc.contributor.authorWang, Yu-Li
dc.date2022-08-11T08:09:36.000
dc.date.accessioned2022-08-23T16:37:10Z
dc.date.available2022-08-23T16:37:10Z
dc.date.issued2001-09-27
dc.date.submitted2009-04-02
dc.identifier.citation<p>Proc Natl Acad Sci U S A. 2001 Sep 25;98(20):11295-300. <a href="http://dx.doi.org/10.1073/pnas.201201198">Link to article on publisher's site</a></p>
dc.identifier.issn0027-8424 (Print)
dc.identifier.doi10.1073/pnas.201201198
dc.identifier.pmid11572981
dc.identifier.urihttp://hdl.handle.net/20.500.14038/38952
dc.description.abstractFocal adhesion kinase (FAK) is a non-receptor protein tyrosine kinase localized at focal adhesions and is believed to mediate adhesion-stimulated effects. Although ablation of FAK impairs cell movement, it is not clear whether FAK might be involved in the guidance of cell migration, a role consistent with its putative regulatory function. We have transfected FAK-null fibroblasts with FAK gene under the control of the tetracycline repression system. Cells were cultured on flexible polyacrylamide substrates for the detection of traction forces and the application of mechanical stimulation. Compared with control cells expressing wild-type FAK, FAK-null cells showed a decrease in migration speed and directional persistence. In addition, whereas FAK-expressing cells responded to exerted forces by reorienting their movements and forming prominent focal adhesions, FAK-null cells failed to show such responses. Furthermore, FAK-null cells showed impaired responses to decreases in substrate flexibility, which causes control cells to generate weaker traction forces and migrate away from soft substrates. Cells expressing Y397F FAK, which cannot be phosphorylated at a key tyrosine site, showed similar defects in migration pattern and force-induced reorientation as did FAK-null cells. However, other aspects of F397-FAK cells, including the responses to substrate flexibility and the amplification of focal adhesions upon mechanical stimulation, were similar to that of control cells. Our results suggest that FAK plays an important role in the response of migrating cells to mechanical input. In addition, phosphorylation at Tyr-397 is required for some, but not all, of the functions of FAK in cell migration.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=11572981&dopt=Abstract">Link to Article in PubMed</a></p>
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC58723/
dc.subjectAnimals
dc.subjectCell Adhesion
dc.subjectCell Movement
dc.subjectCells, Cultured
dc.subjectEmbryo, Mammalian
dc.subjectFibroblasts
dc.subjectFocal Adhesion Kinase 1
dc.subjectFocal Adhesion Protein-Tyrosine Kinases
dc.subjectFocal Adhesions
dc.subjectGreen Fluorescent Proteins
dc.subjectLuminescent Proteins
dc.subjectMetalloproteins
dc.subjectMice
dc.subjectProtein-Tyrosine Kinases
dc.subjectRecombinant Fusion Proteins
dc.subjectTetracycline
dc.subjectTransfection
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleFocal adhesion kinase is involved in mechanosensing during fibroblast migration
dc.typeJournal Article
dc.source.journaltitleProceedings of the National Academy of Sciences of the United States of America
dc.source.volume98
dc.source.issue20
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/1781
dc.identifier.contextkey808546
html.description.abstract<p>Focal adhesion kinase (FAK) is a non-receptor protein tyrosine kinase localized at focal adhesions and is believed to mediate adhesion-stimulated effects. Although ablation of FAK impairs cell movement, it is not clear whether FAK might be involved in the guidance of cell migration, a role consistent with its putative regulatory function. We have transfected FAK-null fibroblasts with FAK gene under the control of the tetracycline repression system. Cells were cultured on flexible polyacrylamide substrates for the detection of traction forces and the application of mechanical stimulation. Compared with control cells expressing wild-type FAK, FAK-null cells showed a decrease in migration speed and directional persistence. In addition, whereas FAK-expressing cells responded to exerted forces by reorienting their movements and forming prominent focal adhesions, FAK-null cells failed to show such responses. Furthermore, FAK-null cells showed impaired responses to decreases in substrate flexibility, which causes control cells to generate weaker traction forces and migrate away from soft substrates. Cells expressing Y397F FAK, which cannot be phosphorylated at a key tyrosine site, showed similar defects in migration pattern and force-induced reorientation as did FAK-null cells. However, other aspects of F397-FAK cells, including the responses to substrate flexibility and the amplification of focal adhesions upon mechanical stimulation, were similar to that of control cells. Our results suggest that FAK plays an important role in the response of migrating cells to mechanical input. In addition, phosphorylation at Tyr-397 is required for some, but not all, of the functions of FAK in cell migration.</p>
dc.identifier.submissionpathoapubs/1781
dc.contributor.departmentDepartment of Physiology
dc.source.pages11295-300


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