Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.690205
Title: Examination of microRNAs in skeletal stem cell differentiation
Author: Cheung, Kelvin
ISNI:       0000 0004 5922 3401
Awarding Body: University of Southampton
Current Institution: University of Southampton
Date of Award: 2015
Availability of Full Text:
Access through EThOS:
Full text unavailable from EThOS. Please try the link below.
Access through Institution:
Abstract:
MicroRNAs (miRNA/miRs) play a crucial role in a variety of biological processes including stem cell differentiation and function. Foetal femur-derived skeletal stem cells (SSCs) display enhanced proliferation and multipotential capacity, indicating excellent potential as candidates for tissue engineering applications. This thesis has identified and characterised subpopulations of skeletal stem cells found within the foetal femur. Cells isolated from the epiphyseal region of the foetal femur expressed higher levels of genes associated with chondrogenesis while cells from the diaphyseal region expressed higher levels of genes associated with osteogenic differentiation. In addition to the difference in osteogenic and chondrogenic gene expression, epiphyseal and diaphyseal cell populations displayed distinct miRs expression profiles. To examine the role of miRNA during skeletogenesis, a robust cell culture model containing differentiating SSCs and an effective transfection protocol was developed. Spermine-pullulan complex, a potential delivery system for miRNA-based gene therapy, was shown to be able to transfect SSCs with miRNA mimics and inhibitors but with lower efficacy compared to liposome base transfection reagent. Through miRNA gene expression profiling and mRNA targets analysis, miR-146a was found to be expressed by diaphyseal cell populations at a significantly enhanced level compared to epiphyseal populations and was predicted to target various components of the TGF-β pathway. Examination of miR-146a function in foetal femur cells confirmed regulation of protein translation of SMAD2 and SMAD3 following transient overexpression in epiphyseal cells. The down-regulation of SMAD2 and SMAD3 following overexpression of miR-146a resulted in an up-regulation of the osteogenesis-related gene RUNX2 and down-regulation of the chondrogenesis-related gene SOX9.In conclusion, this thesis has identified subpopulations of skeletal stem cells with enhanced osteogenic and chondrogenic potential and has explored new miRNA targets involved in skeletogenesis in the attempt to develop novel treatments for patients requiring reparation of the skeletal system.
Supervisor: Oreffo, Richard ; Sanchez-Elsner, Tilman Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.690205  DOI: Not available
Share: