The Contribution of Endogenous and Exogenous Stem Cells in Fracture Repair

dc.contributor.advisorDuncan, Neil A.
dc.contributor.advisorKrawetz, Roman J.
dc.contributor.authorFerrie, Leah Elizabeth
dc.contributor.committeememberMatyas, John Robert
dc.contributor.committeememberRancourt, Derrick E.
dc.date2020-06
dc.date.accessioned2019-12-19T16:42:29Z
dc.date.available2019-12-19T16:42:29Z
dc.date.issued2019-12-17
dc.description.abstractThroughout the lifespan, bone remodels in response to damage, such as fracture. However, diseases such as osteoporosis can cause impaired bone healing, increasing the risk of progression to non-repairing defects called fracture non-unions. Promoting the healing of fracture non-unions is a promising target for bone tissue engineering due to the limited success of current clinical treatment methods. There has been significant research on the use of stem cells with and without biomaterial scaffolds to treat bone fractures due to their promising regenerative capabilities. However, the relative roles of transplanted stem cells (exogenous stem cells) and stem cells found naturally in the body (endogenous stem cells) and their overall contribution to in vivo fracture repair is not well understood, thereby delaying the translation of new tissue engineering therapies to the clinic. The purpose of this research was to determine the interaction between exogenous and endogenous stem cells and biomaterials during bone fracture healing. This study was conducted using a burr-hole fracture model in a mesenchymal stem cell lineaging-tracing mouse. Burr-hole fractures were treated with collagen-I biomaterial loaded with and without green fluorescent protein tagged induced pluripotent stem cells. Using lineage-tracing, the roles of exogenous and endogenous stem cells during bone fracture repair could be elucidated. It was determined that in both a normal and impaired model of fracture healing treatment with exogenous stem cells did not result in improved bone formation and did not promote the recruitment of endogenous stem cells. However, treatment with exogenous stem cells in an impaired model of healing may offer healing advantages compared to in a normal model of healing. The outcomes of this study provide fundamental knowledge required for developing more effective stem cell and biomaterial therapies to treat bone fractures.en_US
dc.identifier.citationFerrie, L. E. (2019). The Contribution of Endogenous and Exogenous Stem Cells in Fracture Repair (Master's thesis, University of Calgary, Calgary, Canada). Retrieved from https://prism.ucalgary.ca.en_US
dc.identifier.doihttp://dx.doi.org/10.11575/PRISM/37347
dc.identifier.urihttp://hdl.handle.net/1880/111356
dc.language.isoengen_US
dc.publisher.facultySchulich School of Engineeringen_US
dc.publisher.institutionUniversity of Calgaryen
dc.rightsUniversity of Calgary graduate students retain copyright ownership and moral rights for their thesis. You may use this material in any way that is permitted by the Copyright Act or through licensing that has been assigned to the document. For uses that are not allowable under copyright legislation or licensing, you are required to seek permission.en_US
dc.subjectBoneen_US
dc.subjectStem cellsen_US
dc.subjectBiomaterialsen_US
dc.subjectFracture repairen_US
dc.subject.classificationEngineering--Biomedicalen_US
dc.titleThe Contribution of Endogenous and Exogenous Stem Cells in Fracture Repairen_US
dc.typemaster thesisen_US
thesis.degree.disciplineEngineering – Biomedicalen_US
thesis.degree.grantorUniversity of Calgaryen_US
thesis.degree.nameMaster of Science (MSc)en_US
ucalgary.item.requestcopytrueen_US
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