[cid:image001.png@01DC4352.DDD97EB0] Wednesday, October 29, 2025 | 9:30 - 10:20am, MJIS 1001 Students registered for the seminar are expected to attend in-person. Teams Meeting ID: 211 123 896 292 8 Passcode: Uh9qs2pf "The Role of Vasa Vasorum in Cerebral Aneurysms - Friend and/or Foe?" [cid:image002.jpg@01DC4352.DDD97EB0] Anne M. Robertson, PhD William Kepler Whiteford Professor of Engineering and Distinguished Service Professor University of Pittsburgh Abstract: Vasa vasorum, or "vessels of the vessels," are essential for supplementing the physiological transport of nutrients from the blood-filled lumen into the arterial wall in areas of the vasculature with high metabolic demands and/or thicker walls. In cerebral arteries, it is believed the vasa vasorum only develops in pathological situations, such as in regions of atherosclerotic driven wall thickening. In this context, they are largely viewed as having a negative influence on cerebral vascular health. Similarly, the presence of vasa vasorum in intracranial aneurysm (IA) walls has generally been viewed negatively, due to an association with inflammation. Moreover, vasa vasorum in IAs have been implicated in continued growth of large and giant aneurysms, after apparently successful endovascular treatment - ultimately necessitating surgical intervention. Enlarging aneurysm must thicken to maintain structural stability and avoid rupture. In our study of 82 human brain aneurysm specimens, harvested during open brain surgery, we found the average IA wall thickness to be 370 ± 220 microns, well above the estimated effective oxygen diffusion distance in arteries. We therefore conjectured vasa vasorum are needed to avoid hypoxia in many IAs. In this study, we took a multi-modal approach to analyze the vasa vasorum in a single brain aneurysm specimen. Using scanning immunofluorescent multiphoton imaging (SI-MPM), we identified, for the first time, an extensive vasorum plexus in the IA wall, in contrast to the morphology of vasa vasorum vessels in cerebral arteries. We found a strong correlation between vasa vasorum and increased wall thickness (R.=0.96, P<0.001), and associations with well-defined biaxially oriented collagen fibers, both consistent with a positive role for the vasa vasorum. A possibly negative influence of the vasa vasorum was related to findings on calcification distribution. Calcification particles were found preferentially located around the vasa vasorum in the IA wall, and large calcifications were found filling the lumen in sections of three out of four vessels entering the vasa vasorum network. We then used computational methods to analyze oxygen transport in the same specimen, employing a micro-CT model of the specimen and high-resolution multi-photon microscopy segmentations of the vasa vasorum network. The results of this study support the crucial role of vasa vasorum in preventing hypoxia in the outer aneurysm wall. Biography: I am an endowed professor of engineering at the University of Pittsburgh and Research Director of the Bio Tissue and Complex Fluid Laboratory where my team is immersed in investigations of pathologies and healing of soft tissues. We use a variety of tools that range across theoretical, computational and experimental frameworks to pioneer work on the biomechanics of soft tissues with a particular emphasis on cerebral aneurysms, arteries, and bladder. Much of our work addresses the relationship between structure (e.g. architecture of the extracellular matrix) and mechanical function (e.g. elasticity, strength) in health and disease. We explore the capacity for even diseased tissue to regenerate and how this capacity is tied to the patient's lifestyle and medical health. To accomplish these goals, my team has developed new mechanical testing and bioimaging methodologies as our needs have arisen during the process of scientific exploration. These efforts have led to advances in our understanding of the role of collagen fibers, elastin, calcification and vascular cells in the biomechanical function of organs including arteries, cerebral aneurysms, bladder and tissue engineered blood vessels. For example, using our custom uniaxial MPM system, we were able to study, for the first time, progressive changes to collagen and elastin architecture during loading in tissue samples without staining, fixation or destructive preparations. Using our approach, we proved a long-standing conjecture about the role of collagen and elastin in the stress stretch curve of arteries. We built this prior work to develop a similar MPM compatible biaxial testing system. This approach has since been used to great advantage for other tissues. ~ BME Host: Vitaliy Rayz~ [cid:image003.png@01DC4352.DDD97EB0] -- Bmeroundtable-list mailing list Bmeroundtable-list@ecn.purdue.edu https://engineering.purdue.edu/ECN/mailman/listinfo/bmeroundtable-list
