Pericyte deficiencies in a foxf2 loss of function mutant

Graff, Merry Faye

Pericyte deficiencies in a foxf2 loss of function mutant

dc.contributor.advisor	Childs, Sarah
dc.contributor.author	Graff, Merry Faye
dc.contributor.committeemember	McFarlane, Sarah
dc.contributor.committeemember	Grewal, Savraj
dc.date	2027-05
dc.date.accessioned	2024-06-27T18:49:32Z
dc.date.available	2024-06-27T18:49:32Z
dc.date.issued	2024-06-26
dc.description.abstract	Pericytes are critical players in vascular development and disease but are not widely studied in the context of cerebral small vessel disease, a vascular condition related to stroke that progressively weakens brain microvessels. Foxf2, a pericyte-expressed gene, is involved in vascular stability and reduced FOXF2 is associated with increased stroke risk and CSVD prevalence. Here, I use a zebrafish foxf2a loss of function mutant as a genetic model of CSVD to show pathological alterations in brain pericytes. Not only are there fewer brain pericytes across the lifespan, but these pericytes also exhibit morphological abnormalities like increased soma size, process length and degeneration. These abnormalities manifest differently in adult brains, and blood vessel defects are evident. I show that embryonic pericyte defects are not the result of decreased pericyte density but a combination of cell-autonomous and non-cell-autonomous effects. A downstream target of foxf2a, loxl2b, is downregulated in foxf2 mutants. While loxl2b mRNA is sufficient to boost brain pericyte numbers, mutants for this gene do not show an obvious phenotype, suggesting a more complicated role. This thesis sheds light on novel lifespan defects in mutant brain pericytes, potentially contributing to vascular destabilization, and opens new avenues for studying genetic forms of human cerebral small vessel disease.
dc.identifier.citation	Graff, M. F. (2024). Pericyte deficiencies in a foxf2 loss of function mutant (Master's thesis, University of Calgary, Calgary, Canada). Retrieved from https://prism.ucalgary.ca.
dc.identifier.uri	https://hdl.handle.net/1880/119045
dc.language.iso	en
dc.publisher.faculty	Graduate Studies
dc.publisher.institution	University of Calgary
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	Pericytes
dc.subject	Vascular Stability
dc.subject	Foxf2
dc.subject	Zebrafish
dc.subject	Loxl2
dc.subject	Endothelium
dc.subject	Cerebral Small Vessel Disease
dc.subject	Development
dc.subject.classification	Education--Sciences
dc.subject.classification	Genetics
dc.subject.classification	Biology
dc.title	Pericyte deficiencies in a foxf2 loss of function mutant
dc.type	master thesis
thesis.degree.discipline	Medicine – Biochemistry and Molecular Biology
thesis.degree.grantor	University of Calgary
thesis.degree.name	Master of Science (MSc)
ucalgary.thesis.accesssetbystudent	I require a thesis withhold – I need to delay the release of my thesis due to a patent application, and other reasons outlined in the link above. I have/will need to submit a thesis withhold application.