Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.616839
Title: Generation of disease-relevant neurons from human pluripotent stem cells
Author: Arber, Charles
Awarding Body: Imperial College London
Current Institution: Imperial College London
Date of Award: 2013
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Abstract:
This thesis describes investigations into exogenous factors that influence fate-choices during human pluripotent stem cell (PSC) differentiation in vitro. I describe novel growth factor environments and small molecule regimes that provide patterning signals enabling directed differentiation of human PSCs towards biomedically relevant neurons. I provide evidence that the TGFβ growth factor Activin can promote ventral telencephalic differentiation. Small adjustments in Activin administration can produce an over-representation of forebrain derived medium spiny neurons and cortical interneurons, with significance in Huntington’s disease and epilepsy respectively. Additionally, I manipulate the earliest growth factor environments of PSC differentiation to lead to broad changes in rostro-caudal patterning. Inhibiting FGF signalling leads to a midbrain-like phenotype that can be further differentiated towards a ventral midbrain dopaminergic fate, a cell type that degenerates in Parkinson’s disease. Our novel manipulations and differentiation protocols provide insights into early events in human development, which would otherwise be impossible to study. This logic can also be applied to investigate diseased states during human development and ageing via use of disease-specific cell lines. The mature neurons produced may provide a tool that can be applied to large-scale drug screening assays and toxicology testing as well as having the potential for cell based therapies in future years.
Supervisor: Li, Meng Sponsor: Medical Research Council ; EuroStemCell ; Imperial College London
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.616839  DOI: Not available
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