Spatial and Temporal Diversity of Astrocyte Phenotypes in Spinocerebellar Ataxia Type 1 Mice

• Published in: Cells (Basel, Switzerland) Switzerland), 2022-10, Vol.11 (20), p.3323
• Main Authors: Rosa, Juao-Guilherme, Hamel, Katherine, Sheeler, Carrie, Borgenheimer, Ella, Gilliat, Stephen, Soles, Alyssa, Ghannoum, Ferris J, Sbrocco, Kaelin, Handler, Hillary P, Rainwater, Orion, Kang, Ryan, Cvetanovic, Marija
• Format: Article
• Language: English
• Subjects: Alzheimer's disease; Analysis; Animals; Astrocytes; Astrocytes - metabolism; Ataxia; Ataxin; Ataxin-1 - genetics; Ataxin-1 - metabolism; Brain; Brain stem; Care and treatment; Cerebellum; Cerebellum - metabolism; Cortex (motor); Cortex (temporal); Diagnosis; Gene expression; Genetic aspects; Glial fibrillary acidic protein; Homeostasis; Mice; Microglia; Morphology; Neurodegeneration; Neurodegenerative diseases; Pathogenesis; Pathology; Phenotype; Phenotypes; Polyglutamine; Proteins; RNA sequencing; SCA1; Spinocerebellar ataxia; Spinocerebellar Ataxias - genetics; Spinocerebellar Ataxias - pathology; Trinucleotide repeat diseases; Trinucleotide repeats
• ISSN: 2073-4409; 2073-4409
• DOI: 10.3390/cells11203323

While astrocyte heterogeneity is an important feature of the healthy brain, less is understood about spatiotemporal heterogeneity of astrocytes in brain disease. Spinocerebellar ataxia type 1 (SCA1) is a progressive neurodegenerative disease caused by a CAG repeat expansion in the gene ( ). We characterized astrocytes across disease progression in the four clinically relevant brain regions, cerebellum, brainstem, hippocampus, and motor cortex, of mice, a knock-in mouse model of SCA1. We found brain region-specific changes in astrocyte density and GFAP expression and area, early in the disease and prior to neuronal loss. Expression of astrocytic core homeostatic genes was also altered in a brain region-specific manner and correlated with neuronal activity, indicating that astrocytes may compensate or exacerbate neuronal dysfunction. Late in disease, expression of astrocytic homeostatic genes was reduced in all four brain regions, indicating loss of astrocyte functions. We observed no obvious correlation between spatiotemporal changes in microglia and spatiotemporal astrocyte alterations, indicating a complex orchestration of glial phenotypes in disease. These results support spatiotemporal diversity of glial phenotypes as an important feature of the brain disease that may contribute to SCA1 pathogenesis in a brain region and disease stage-specific manner.