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dc.contributor.advisorRoger D. Kamm.en_US
dc.contributor.authorKris, Anita Sen_US
dc.contributor.otherMassachusetts Institute of Technology. Biological Engineering Division.en_US
dc.date.accessioned2008-09-03T15:30:48Z
dc.date.available2008-09-03T15:30:48Z
dc.date.copyright2007en_US
dc.date.issued2007en_US
dc.identifier.urihttp://hdl.handle.net/1721.1/42386
dc.descriptionThesis (M. Eng.)--Massachusetts Institute of Technology, Biological Engineering Division, 2007.en_US
dc.descriptionIncludes bibliographical references (p. 57-60).en_US
dc.description.abstractCells respond to the application of force with a variety of biochemical responses modulating their shape, structure, function, and proliferation. Two force-responsive links between the inside and outside of a cell are integrin proteins, which link a cell to the extracellular matrix (ECM), and cadherin proteins, which link neighboring cells to each other. The strength of integrin-ECM bonds has been noted to increase in response to the application of force. However, the strengthening of cadherin-cadherin bonds in response to force has not been studied. Here, we use magnetic trapping to probe adhesion strengthening at cadherin adherens junctions, using cadherin-coated magnetic beads to simulate neighboring cells and apply force at adherens junctions. 43% of beads exposed to a high force (2.1 nN) detached, compared to 31% of those exposed to a low-to-high force ramp followed by high force. This indicates that adherens junctions are strengthened by force application. The actin cytoskeleton and vasodilator-stimulated phosphoprotein (VASP) both associate with adherens junctions, so their role in adhesion strengthening at adherens junctions was also studied. Cells treated with actin-inhibitor cytochalasin D showed no difference in bead detachment from constant high force and from ramped followed by high force, indicating that the actin cytoskeleton is crucial in the adhesion strengthening response. Beads attached to cells expressing GFP-VASP, which behave like VASP-overexpressing cells, detached in 24% of trials when exposed to constant high force, compared to 39% of trials in response to ramped force. Cells expressing GFP-MITO-FPPPP, which behave like VASP-downregulated cells, showed no difference in bead detachment between application of high force and ramped force followed by high force.en_US
dc.description.abstract(cont.) These experiments indicate that VASP is necessary for the adhesion strengthening response, but high levels of VASP may slow actin restructuring and diminish the ability of the cytoskeletal linkages to respond to increasing force. The importance of VASP in cells' responses to forces from other cells suggest that modulation of VASP activity may play a role in tissue development, where cell-cell force responses are important, and the pathogenesis of certain diseases, where cell-cell adhesion is affected.en_US
dc.description.statementofresponsibilityby Anita S. Kris.en_US
dc.format.extent60 p.en_US
dc.language.isoengen_US
dc.publisherMassachusetts Institute of Technologyen_US
dc.rightsMIT theses may be protected by copyright. Please reuse MIT thesis content according to the MIT Libraries Permissions Policy, which is available through the URL provided.en_US
dc.rights.urihttp://dspace.mit.edu/handle/1721.1/7582en_US
dc.subjectBiological Engineering Division.en_US
dc.titleForce-mediated adhesion strengthening in endothelial cells at adherens junctionsen_US
dc.typeThesisen_US
dc.description.degreeM.Eng.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineering
dc.identifier.oclc234558913en_US


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