Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.729435
Title: Validation of a three-dimensional culture system for the differentiation of multipotential mesenchymal stromal cells by uniaxial strain
Author: Parker, Lindsey Christine
ISNI:       0000 0004 6494 5871
Awarding Body: University of Leeds
Current Institution: University of Leeds
Date of Award: 2017
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Abstract:
The differentiation potential of multipotential mesenchymal stromal cells is known to be affected by many aspects of the cellular microenvironment, including soluble factors, extracellular matrix composition, the Young’s modulus of the substrate, cellular neighbours and externally applied forces. Despite this, reasonable understanding of harnessing soluble factors only exists. Few studies have investigated mechanotransduction in hMSC, and those published to date primarily employ unsuitable substrates, that do not facilitate the cellular adhesions known to be active in force transmission. In this study, porcine pericardium was decellularised for use as a biologically-relevant, threedimensional scaffold for the mechanostimulation of hMSC in a uniaxial strain bioreactor. Tissue stocks (n=67) were successfully decellularised and confirm biocompatible, sterile and free of contaminating genomic DNA. Histoarchitecture comparable to that of native tissue was also maintained. Tencell-specific seeding rings were found to release cytotoxic residue, and an alternative, nontoxic seeding approach was developed. The Tencell bioreactor was initially unable to maintain cell viability as a culture system, and was validated with respect to chamber humidity, culture temperature and arm displacement. Temperature maintenance was inadequate prior to re-engineering of the heating apparatus and was rectified through the use of an autotunable module. Losses of cell viability were still observed following validation as a result of medium pH changes. A Tencell culture regime utilising the HEPES buffer was successfully developed for the culture of hMSC. No significant differences in gene expression between strained and unstrained samples were found, and the greatest effects were observed between unseeded and other sample types. Additionally, seeded hMSC did not penetrate the scaffold. Overall, this study investigated the differentiation potential of hMSC cultured in a threedimensional scaffold. The Tencell bioreactor was fully validated for use as a uniaxial strain mechanostimulation device, and could be used in future studies to investigate the effect of different frequencies and magnitudes of cyclic strain.
Supervisor: Ingham, Eileen ; Thomas, Dan ; Fisher, John Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.729435  DOI: Not available
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