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dc.contributor.advisorClark K. Colton.en_US
dc.contributor.authorTan, Jit Hinen_US
dc.contributor.otherMassachusetts Institute of Technology. Department of Chemical Engineering.en_US
dc.date.accessioned2013-11-18T17:35:54Z
dc.date.available2013-11-18T17:35:54Z
dc.date.copyright2013en_US
dc.date.issued2013en_US
dc.identifier.urihttp://hdl.handle.net/1721.1/82175
dc.descriptionThesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Chemical Engineering, 2013.en_US
dc.descriptionThis electronic version was submitted by the student author. The certified thesis is available in the Institute Archives and Special Collections.en_US
dc.descriptionCataloged from student-submitted PDF version of thesis.en_US
dc.descriptionIncludes bibliographical references (p. 133-151).en_US
dc.description.abstractCell-to-cell variability in clonal populations is reflected in a distribution of mRNA and protein levels among individual cells, including those of key transcription factors governing embryonic stem cell (ESC) pluripotency and differentiation. This may be a source of heterogeneity resulting in mixtures of cell types in differentiated populations despite efforts to control the differentiation conditions and the use of a clonal starting population. In addition, this distribution may be affected by the cell microenvironment during self-renewal. Prior studies on self-renewal culture of ESC, however, focused on long term proliferation and pluripotency. The effects of culture conditions during self-renewal on the effectiveness of subsequent differentiation protocols remains understudied. Using a mouse ESC line harboring a GFP reporter, we examined cell-to-cell variability in clonal undifferentiated populations and how such variability affects subsequent differentiation. Subpopulations sorted according to their levels of Oct4-GFP expression displayed distinctly different expression levels of pluripotency and early differentiation markers and differentiated into cardiomyocytes at different efficiencies. However, when allowed to self-renew after sorting, the subpopulations regenerated the parental distributions of Oct4-GFP and subsequent differentiation after regeneration did not show differences. In addition to differences between cells in a clonal population, self-renewal conditions affecting Oct4 expression on the population-level were examined. Changes in culture conditions during self-renewal by low oxygen culture or small molecule dual inhibition (2i) of mitogen-activated protein kinase and glycogen synthase kinase reversibly affected levels of Oct4 expression in cells that were otherwise pluripotent. Effects of different self-renewal conditions immediately preceding differentiation are manifested by changes in subsequent differentiation to cardiomyocytes. This study demonstrates that manipulation of self-renewal culture conditions can lead to changes in the outcomes of defined differentiation protocols, a novel dimension to explore for directed differentiation of pluripotent stem cells.en_US
dc.description.statementofresponsibilityby Jit Hin Tan.en_US
dc.format.extent151 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.subjectChemical Engineering.en_US
dc.titleCell-to-cell variability and culture conditions during self-renewal reversibly affect subsequent differentiation of mouse embryonic stem cellsen_US
dc.typeThesisen_US
dc.description.degreePh.D.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineering
dc.identifier.oclc861633997en_US


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