Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.793173
Title: Development of multi-layered models of the airway mucosa
Author: Tait, Angela
ISNI:       0000 0004 8501 6959
Awarding Body: University of Southampton
Current Institution: University of Southampton
Date of Award: 2014
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Abstract:
Introduction: Asthma is a global burden, leading to around 180,000 deaths worldwide annually. Translation of therapies from animal models is limited, suggesting these models do not recapitulate adequately genetic and environmental aspects of asthma. Existing human cell culture models are usually simplistic and do not mimic the in vivo tissue architecture; therefore there is a need to improve three-dimensional human tissue culture models. We hypothesised that use of cell sheet engineering would help overcome this problem. Aims: Thermoresponsive polymers or ultrasound standing waves (Sonotweezers) will be tested for their compatibility for the formation of cell sheets which can be used for tissue engineering. Methods: Poly (2-alkyl-2-oxazolines) are polymers with thermoresponsive properties and were tested for biocompatibility using cell motility and adhesion assays, immunofluorescent staining, and measurement of p38 phosphorylation. Multiple cell types were seeded onto thermoresponsive polymers (either NiPAAm, poly(2-alkyl-2-oxazolines) or thermo-gels of poly(2-isopropyl-2-oxazoline)-carboxymethylcellulose)) and cell sheet release assessed after incubation at 20ºC. Cell sheets were also created using ultrasound standing waves (Sonotweezers) or incubation on a thermo-gel. Adhesion junctions in cell sheets were assessed by staining for E-cadherin, ZO-1 and the actin cytoskeleton; cell viability was monitored using 7-Aminoactinomycin D. Subsequently, epithelial cell sheets were used to created co-cultures with fibroblasts. Cytokine release (IL-6 and IP-10) following Poly (I:C) stimulation from cell-sheet co-cultures was compared to conventional models by ELISA. Results: Using conventional cell culture techniques a multi-layered cell structure by the addition of epithelial cells onto a confluent fibroblast layer was not possible as it resulted in redistribution of the cells to form a single layer comprising islands of epithelial cells surrounded by fibroblasts. Consequently alternative methods were explored using thermoresponsive polymers or Sonotweezers. Cells could be lifted from a commercial NiPAAm coated dish (UpCell) after attachment to a membrane, but during the release process cells either rounded up and lost contact (fibroblasts, HeLa cells) or epithelial cell sheets were damaged and incompletely released. Sonotweezers also could not generate sufficient force to release and levitate the cells. As alternatives, cell sheets were created by levitation in the Sonotweezers device or overlaying the cells on a thermo-gel to allow cell sheet formation followed by sedimentation onto an underlying layer of fibroblasts. Levitation of single cells resulted in the formation of a cell sheet within 2 hours, which gradually contracted becoming three-dimensional by 24 hours. Contraction could be inhibited by removal of Ca2+ to prevent adherens junction formation or by adding cytochalasin D to prevent actin filaments or an E-cadherin neutralising antibody to prevent adherens junction formation. After 2 hours of levitation, the cell sheet could be placed onto confluent MRC5 fibroblasts and epithelial cells used plithotaxis to spread across the fibroblasts to create two distinct layers. Oxazoline polymers with a range of hydrophobicities covalently attached to glass were biocompatible, but not thermoresponsive. A gel of poly(2-isopropyl-2-oxazoline-co-2-butyl2-oxazoline)-carboxymethylcellulose was thermoresponsive, enabling formation of epithelial cell sheets which were used to form cell-sheet co-cultures. The cell-sheet co-cultures achieved an electrically tight barrier and when challenged with the viral mimic Poly(I:C), showed increased IL-6 and IP-10 release. IL-6 release was predominantly apical, whereas IP-10 was basolateral, suggesting polarised mediator release. Conclusions: Multi-layered cell culture models can be created using either the Sonotweezers device or gelling polymers. The latter offers potential for formation of multi-layered structures in a high through-put manner.
Supervisor: Davies, Donna ; Hill, Martyn Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.793173  DOI: Not available
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