Abstract TP297: Focused Mouse Brain Irradiation Model to Define the Neurovascular Unit

Abstract

Purpose: This project aimed to develop a stereotactic radiosurgery mouse model of radiation-induced brain injury to study endothelial damage within the neurovascular unit (NVU). Classification of focal endothelial damage and the resulting inflammatory cascade has never been cataloged for assessing intrinsic changes versus extrinsic factors of inflammation at the NVU. The study of endothelial damage with invasive models, such as open transcranial injury or vessel occlusion, introduces multiple variables into the system that our model can help overcome to study secondary or systemic insults of the NVU. Methods: Using an X-ray image-guided radiation therapy system, mice were focally irradiated with 30, 45, and 70 Gy to a 5 mm brain target. Mice were followed up at 2, 4, 6, 12 and 18 weeks after irradiation with contrast-enhanced CT imaging for volumetric quantification of radiation effects. Brains were harvested for characterization by histology and immune-multiplexing of reactionary and inflammatory changes to the NVU. Whole coronal slides were scanned and analyzed using machine learning classifiers to quantify cell types within the NVU in the radiated vs. control hemispheres. Results: Radiation-induced changes such as telangiectasias, vessel hyalinization, and white matter necrosis were observed. An inflammatory response with a predominance of T cells was observed, as well as an increase in microglial cells and reactive astrogliosis. These changes were time and dose-dependent after radiation. Serial CTs allowed for determining the development of radiation damage, and the contrast enhancement was proportional to the degree of radiation-induced changes. Conclusions: This radiation model allows precise image-guided targeting with a steep radiation fall-off into surrounding tissues. The NVU’s response to focal insult of endothelial damage presents a novel method of brain injury to specifically study diseases associated with endothelial dysfunction.