Cranial irradiation disrupts homeostatic microglial dynamic behavior

• Published in: Journal of neuroinflammation Vol. 21; no. 1; p. 82
• Main Authors: Strohm, Alexandra O, Johnston, Carl, Hernady, Eric, Marples, Brian, O'Banion, M Kerry, Majewska, Ania K
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 03-04-2024; BioMed Central; BMC
• Subjects: Brain research; Cognitive ability; Environmental monitoring; Genetic engineering; Health aspects; Homeostasis; Homeostatic plasticity; Irradiation; Methods; Microglia; Microglial cells; Morphology; Neural plasticity; Parenchyma; Radiation; Skull; Statistical significance; Transgenic mice; Two-photon microscopy; United States; Two-photon microscopy; Radiation; Microglia
• ISSN: 1742-2094; 1742-2094
• DOI: 10.1186/s12974-024-03073-z

Cranial irradiation causes cognitive deficits that are in part mediated by microglia, the resident immune cells of the brain. Microglia are highly reactive, exhibiting changes in shape and morphology depending on the function they are performing. Additionally, microglia processes make dynamic, physical contacts with different components of their environment to monitor the functional state of the brain and promote plasticity. Though evidence suggests radiation perturbs homeostatic microglia functions, it is unknown how cranial irradiation impacts the dynamic behavior of microglia over time. Here, we paired in vivo two-photon microscopy with a transgenic mouse model that labels cortical microglia to follow these cells and determine how they change over time in cranial irradiated mice and their control littermates. We show that a single dose of 10 Gy cranial irradiation disrupts homeostatic cortical microglia dynamics during a 1-month time course. We found a lasting loss of microglial cells following cranial irradiation, coupled with a modest dysregulation of microglial soma displacement at earlier timepoints. The homogeneous distribution of microglia was maintained, suggesting microglia rearrange themselves to account for cell loss and maintain territorial organization following cranial irradiation. Furthermore, we found cranial irradiation reduced microglia coverage of the parenchyma and their surveillance capacity, without overtly changing morphology. Our results demonstrate that a single dose of radiation can induce changes in microglial behavior and function that could influence neurological health. These results set the foundation for future work examining how cranial irradiation impacts complex cellular dynamics in the brain which could contribute to the manifestation of cognitive deficits.