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Please use this identifier to cite or link to this item: http://hdl.handle.net/11375/20614
Title: The Role of the Vasculature and Immune System in Models of Glaucoma
Authors: Sabljic, Thomas F.
Advisor: Ball, Alexander K.
Department: Neuroscience
Keywords: Glaucoma;Optic Nerve Crush;Retinal Ganglion Cells;Elevated Intraocular Pressure;Vasculature;Immune System;Neurodegeneration;Glial Cells
Publication Date: 18-Nov-2016
Abstract: Purpose: The purpose of this study was to investigate the role of the vasculature and immune system in models of glaucoma. Vascular changes have been implicated in glaucoma. As well there is mounting evidence that the immune system plays a role in the disease. It is my hypothesis that the vasculature and immune system play a role in the retinal response to injury in models of glaucoma. Methods: Immunohistochemistry, in vivo retinal imaging (Bright field, fluorescent, optical coherence tomography), Slit2 injections and Evan’s blue labeling were used to investigate vascular and immune changes associated with retinal ganglion cell death after optic nerve crush up to 28 days after injury. Histology, immunohistochemistry, and intravascular labeling were utilized to investigate the role of the vascular degeneration and the systemic immune response to elevated intraocular pressure in 8-16 week old AP-2β Neural Crest Cell Knockout (AP-2β NCC KO) mice. Results: The vascular and immune responses to optic nerve crush were not found to play a significant role in the response to retinal ganglion cell death. Conversely the role of vascular degeneration and immune cell recruitment to the retinas of AP-2β NCC KO mice demonstrated that these factors played a significant role in the retinal response to injury. Conclusion: The vasculature and immune system play a varied role in the response to retinal injury and neurodegeneration depending on the model being studied. The vascular and immune changes were of minimal significance in acute optic nerve crush injury. On the other hand, the chronic injury associated with elevated intraocular pressure in AP-2β NCC KO mice was associated with significant vascular degeneration and systemic immune cell infiltration.
URI: http://hdl.handle.net/11375/20614
Appears in Collections:Open Access Dissertations and Theses

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