Hald, Eric2017-11-272017-11-272016-08https://hdl.handle.net/11299/191352University of Minnesota Ph.D. dissertation. August 2016. Major: Biomedical Engineering. Advisor: Patrick Alford. 1 computer file (PDF); xi, 118 pages.Vascular disease is a common cause of death that typically results from long-term alteration of vessel structure and function. The underlying mechanisms that lead to pathologic changes in the vasculature are largely unclear, especially in progressive diseases of the cerebral vessels. With the growing prevelance of blast traumatic brain injury in modern warfare, never before has investigation of cerebral vascular disease been more pertinent. Here, we focus on the development of microfabrication experimental approaches for probing the critical mechanical and biochemical pathways involved in progression of diseases, such as cerebral vasospasm, subarachnoid hemorrhage, and Alzheimer’s disease, that often result from TBI. First, we develop a microfluidic patterned deposition technique for studying functional mechanics in chronic vascular disease at the tissue scale. We modify substrate surfaces with genipin, a natural crosslinker, to extend culture times of in vitro vascular tissues that mimic native tissue structure and function. We successfully validate our technique, showing maintenance of patterned structural alignment and mechanical function over the course of two weeks. Lastly, we investigate the relationship between vascular disease and Alzheimer’s disease. Amyloid beta is a key precursor in the development of Alzheimer’s disease that accumulates in neuronal and cerebrovascular tissue and can result in neurodegeneration. During the development of cerebral amyloid angiopathy (CAA), which is present in over 80% of Alzheimer's disease cases, amyloid beta plaques form in the cerebral vessel walls and lead to severe attenuation of physiologic vasodilation. We measured the effect of amyloid beta treatment on vascular smooth muscle cell functional contractility using a single-cell traction force microscopy technique and developed a thin-walled arterial model for growth and remodeling response to mechanical perturbations. We found that amyloid beta induces a reduction in vascular smooth muscle cell mechanical output. We implemented this loss of function into a constrained mixture arterial model that suggests vessel growth and remodeling, in response to amyloid beta-mediated alteration of smooth muscle function, can lead to an inability of cerebral vessels to vasodilate. Our findings provide a possible explanation for the vascular injury and malfunction often associated with the development of neurodegeneration in Alzheimer’s disease.enAlzheimer's diseasegrowth and remodelingin vitro disease modelmicrofabricationvascular mechanicsvascular smooth muscle cellsThesis or Dissertation