Synthetic cell-based patterning systems and their applications in stem cell differentiation
dc.contributor.advisor
Davies, Jamie
dc.contributor.advisor
Dzierzak, Elaine
dc.contributor.author
Glykofrydis, Fokion
dc.contributor.sponsor
Engineering and Physical Sciences Research Council (EPSRC)
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dc.date.accessioned
2021-09-02T14:49:23Z
dc.date.available
2021-09-02T14:49:23Z
dc.date.issued
2020-11-30
dc.description.abstract
Pattern formation underpins cell specification, tissue organization, and morphogenesis
during embryonic development. Tissue engineering strategies based on stem cell
differentiation and organoid formation attempt to recapitulate developmental patterning,
but suffer from variable efficiency, limited complexity, and anatomical disorganization.
Whereas considerable research has focused on understanding patterning in vivo,
bottom-up efforts in engineering synthetic niches to control patterning in vitro have been
limited. This thesis explores a synthetic biology-based approach to create self-organizing
mammalian cell systems, and use them as signalling centres for stem cell applications.
The first half of the thesis explores whether integrin-ligand heterotypic adhesions can
drive the formation of hyperuniform patterns. HEK-293 derivative cell lines were bio-engineered to overexpress heterophilic cell adhesion molecules in a drug-inducible
manner using CRISPR genome editing. Transgenic systems were characterized in input
sensitivity, output strength, adhesion properties, and their ability to form hyperuniform
distributions. The second half of the thesis explores applications of self-organizing cell
systems to control stem cell decisions. A pre-established phase-separation patterning
system was modified to produce WNT3A from multicellular groups, which self-organize
with mouse embryonic stem cells and elicit polarized signalling events. When
differentiated in self-organizing co-cultures, embryonic stem cells exhibit enhanced and
spatially controlled mesoderm induction in 2D and 3D conditions respectively, due to
exogenous, localized Wnt signalling. WNT3A producers can also trigger nephrogenesis
in mouse metanephric mesenchyme, demonstrating their wider applicability. This work
provides novel prototype platforms and conceptual approaches to control developmental
cell fate decisions and organization in vitro, contributing to the generation of synthetic
niches.
en
dc.identifier.uri
https://hdl.handle.net/1842/37977
dc.identifier.uri
https://doi.org/10.7488/era/1248
dc.language.iso
en
en
dc.publisher
The University of Edinburgh
en
dc.relation.hasversion
Davies, J. A., & Glykofrydis, F. (2020). Engineering pattern formation and morphogenesis. Biochemical Society Transactions. https://doi.org/10.1042/BST20200013
en
dc.relation.hasversion
Kauts, M. L., De Leo, B., Rodríguez-Seoane, C., Ronn, R., Glykofrydis, F., Maglitto, A., Kaimakis, P., Basi, M., Taylor, H., Forrester, L., Wilkinson, A. C., Göttgens, B., Saunders, P., & Dzierzak, E. (2018). Rapid Mast Cell Generation from Gata2 Reporter Pluripotent Stem Cells. Stem Cell Reports, 11(4), 1009–1020. https://doi.org/10.1016/j.stemcr.2018.08.007
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dc.subject
protein-signal WNT3A
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dc.subject
cultured stem cells
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dc.subject
integrin-ligand heterotypic adhesions
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dc.subject
hyperuniform patterns
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dc.subject
CRISPR genome editing
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dc.subject
WNT3A
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dc.title
Synthetic cell-based patterning systems and their applications in stem cell differentiation
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dc.type
Thesis or Dissertation
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dc.type.qualificationlevel
Doctoral
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dc.type.qualificationname
PhD Doctor of Philosophy
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