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Exploring cell-substrate interactions in stem cell self-renewal and differentiation

Tissue engineering aims to replace diseased or damaged tissue, one approach for which is to implant cells and a scaffold developed in vitro. One of the engineering challenges is the design of the cell-material interface. Cells respond to a wide range of signals from their substrate, which can be used to control cell behaviour and improve the properties of the implant. Of particular interest to regenerative medicine is that substrate properties can influence stem cell self-renewal and differentiation. This thesis aimed to first better understand how substrate properties such as chemical composition and topography affect stem cell behaviour. For this, two substrates were studied: one with micrometre scale topography, and one with varying chemical composition and nanometre scale topography, for their effect on murine embryonic stem cell (ESC) self-renewal and early differentiation. On micrometre scale topography, the first example of central pit formation due to substrate cues was observed, and the substrates mitigated endoderm specification. On nanometre scale topography, ESC early differentiation markers were diminished, and both substrate topography and chemical composition affected cell behaviour. Then attention was shifted to how biological cues from the substrate, such as ligands specific to cell surface receptors, could guide stem cell chondrogenic differentiation. In that study, the changing adhesion requirements of human mesenchymal stem cells were studied in the form of integrin transcript expression and finally, the role of one specific integrin was shown to affect chondrogenic differentiation in vitro. This was the first complete characterisation of integrin expression and the first demonstration of the role of integrin αvβ8 in chondrogenic differentiation. Overall, these results improve the understanding of how stem cells respond to substrate cues, including some of the crucial cues they require in differentiation, and could therefore be used to improve the design of tissue engineering scaffolds.

Identiferoai:union.ndltd.org:bl.uk/oai:ethos.bl.uk:616860
Date January 2013
CreatorsLaPointe, Vanessa Lydia Simone
ContributorsStevens, Molly
PublisherImperial College London
Source SetsEthos UK
Detected LanguageEnglish
TypeElectronic Thesis or Dissertation
Sourcehttp://hdl.handle.net/10044/1/14769

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