Characterization of the Dedifferentiated Schwann Cell and Development of a Deprogramming-Strategy to Enhance Their Regenerative Capacity
atmire.migration.oldid | 4673 | |
dc.contributor.advisor | Biernaskie, Jeff | |
dc.contributor.author | Stykel, Morgan | |
dc.contributor.committeemember | Ousman, Shalina | |
dc.contributor.committeemember | Whelan, Patrick | |
dc.contributor.committeemember | Schuurmans, Carol | |
dc.contributor.committeemember | Chan, Jennifer | |
dc.date.accessioned | 2016-07-22T21:48:41Z | |
dc.date.available | 2016-07-22T21:48:41Z | |
dc.date.issued | 2016 | |
dc.date.submitted | 2016 | en |
dc.description.abstract | A striking feature of the peripheral nervous system is the ability to regenerate; this ability is, in part, due to the Schwann cell, the glial cell of the periphery. Following peripheral injury, Schwann cells up-regulate a battery of proteins, many of which are re-expressed from development, that drive the efficient regenerative response in the peripheral nervous system. My work described in this thesis characterizes the gene expression profile driving this regenerative response as well as factors implicated during Schwann cell development. Then, I began to develop a deprogramming-based approach to modulate the Schwann cell phenotype by overexpressing the factors of interest. I optimized a deprogramming strategy that can be used to further elucidate the functional contribution of various transcription factors in adult Schwann cells. This can also enhance Schwann cell function following circumstances such prolonged denervation, disease, or advanced aged which often results in impaired regenerative function. | en_US |
dc.identifier.citation | Stykel, M. (2016). Characterization of the Dedifferentiated Schwann Cell and Development of a Deprogramming-Strategy to Enhance Their Regenerative Capacity (Master's thesis, University of Calgary, Calgary, Canada). Retrieved from https://prism.ucalgary.ca. doi:10.11575/PRISM/25292 | en_US |
dc.identifier.doi | http://dx.doi.org/10.11575/PRISM/25292 | |
dc.identifier.uri | http://hdl.handle.net/11023/3150 | |
dc.language.iso | eng | |
dc.publisher.faculty | Graduate Studies | |
dc.publisher.institution | University of Calgary | en |
dc.publisher.place | Calgary | en |
dc.rights | University 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. | |
dc.subject | Neuroscience | |
dc.subject.classification | Schwann cell | en_US |
dc.subject.classification | Transcription Factors | en_US |
dc.subject.classification | Reprogramming | en_US |
dc.subject.classification | Peripheral Nerve Injury | en_US |
dc.subject.classification | Regeneration | en_US |
dc.subject.classification | PNS | en_US |
dc.title | Characterization of the Dedifferentiated Schwann Cell and Development of a Deprogramming-Strategy to Enhance Their Regenerative Capacity | |
dc.type | master thesis | |
thesis.degree.discipline | Neuroscience | |
thesis.degree.grantor | University of Calgary | |
thesis.degree.name | Master of Science (MSc) | |
ucalgary.item.requestcopy | true |