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dc.contributor.advisorKrystyn J. Van Vliet.en_US
dc.contributor.authorBruce, Christopher Men_US
dc.contributor.otherMassachusetts Institute of Technology. Dept. of Materials Science and Engineering.en_US
dc.date.accessioned2010-09-01T13:35:44Z
dc.date.available2010-09-01T13:35:44Z
dc.date.copyright2008en_US
dc.date.issued2008en_US
dc.identifier.urihttp://hdl.handle.net/1721.1/57970
dc.descriptionThesis (S.B.)--Massachusetts Institute of Technology, Dept. of Materials Science and Engineering, 2008.en_US
dc.descriptionCataloged from PDF version of thesis.en_US
dc.descriptionIncludes bibliographical references (p. 27-28).en_US
dc.description.abstractControlling cell behavior has been a primary goal for scientists, and physical interactions, specifically cell-surface interactions, have the potential to be a robust system for cell control. Much research has been conducted on the effect of substrata stiffness on cell behavior, but there has been no systematic study of the effect of varying substrata thickness, and its correlation to a substratum's effective stiffness that a cell feels. Furthermore, there have been differing views on what the critical thickness of a substrate is, above which there will be no difference in cell behavior. An experimental study was carried out to determine the effects of substratum thickness on the behavior of cells adhering to polyacrylamide thin film gels functionalized with gelatin. Relatively compliant thin film gels, with an elastic modulus E ~ 5 kPa, were varied in thickness on stiff glass supports from ~75 nm to 60 microns. 3T3 fibroblast cells were seeded onto the gels to observe differences in behavior. Observed cell behaviors were the projected area of the cells on the surface due to adhesive spreading and the rate of reduction of Alamar Blue dye, which correlates to the proliferation, or growth rate, of the cells. It was found that the cell area had a fairly welldefined power-law dependence on substrate thickness, while the gel thickness did not have a detectable effect on the rate of proliferation of the cells. Additionally, a theoretical model for thin film deflection was fit to the cell area data, and it described the areathickness relationship well.en_US
dc.description.abstract(cont.) By using the theoretical model, a critical thickness of 2.3 tm was identified over which average cell area would not change significantly. This critical thickness was found to be on the order of the reported length scale of focal adhesions in the cells, not the lateral dimensions of the cell. These results are useful in establishing a practical lower limit of'film thickness for normal cell behavior. Additionally, this relationship could be exploited as a way to control stem cell differentiation, cell size, cell motility, cell ligand density, and other cell behaviors.en_US
dc.description.statementofresponsibilityby Christopher M. Bruce.en_US
dc.format.extent28 p.en_US
dc.language.isoengen_US
dc.publisherMassachusetts Institute of Technologyen_US
dc.rightsM.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.en_US
dc.rights.urihttp://dspace.mit.edu/handle/1721.1/7582en_US
dc.subjectMaterials Science and Engineering.en_US
dc.titleExperimental determination of cell adhesion and proliferation response to substrata thicknessen_US
dc.typeThesisen_US
dc.description.degreeS.B.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Materials Science and Engineering
dc.identifier.oclc618653413en_US


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