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  3. Margaret Schroeder’s Thesis Defense: Astrocyte regional specialization is shaped by postnatal development
Margaret Schroeder’s Thesis Defense: Astrocyte regional specialization is shaped by postnatal development
Department of Brain and Cognitive Sciences (BCS)

Margaret Schroeder’s Thesis Defense: Astrocyte regional specialization is shaped by postnatal development

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Add to CalendarAmerica/New_YorkMargaret Schroeder’s Thesis Defense: Astrocyte regional specialization is shaped by postnatal development10/25/2024 2:00 pm10/25/2024 2:00 pmBuilding 46,Singleton Auditorium, Room 3002
October 25, 2024
2:00 pm
Location
Building 46,Singleton Auditorium, Room 3002
    Description

    Date: Friday, 10/25

    Time: 2-3pm

    Location: Singleton Auditorium (46-3002) (and Zoom, see link below)

    Zoom: https://mit.zoom.us/j/91526155715

    Title: Astrocyte regional specialization is shaped by postnatal development

    Abstract: Astrocytes are an abundant class of glial cells with critical roles in neural circuit assembly and function. Though many studies have uncovered significant molecular distinctions between astrocytes from different brain regions, the developmental trajectory of this regional heterogeneity requires further systematic study. To address this knowledge gap, we used single-nucleus RNA sequencing to characterize the molecular diversity of brain cells across six developmental stages and four brain regions in the mouse and marmoset brain. Our analysis of over 170,000 single astrocyte nuclei revealed striking regional heterogeneity among astrocytes, particularly between telencephalic and diencephalic regions, at all developmental time points surveyed in both species. At the stages sampled, most of the region patterning was private to astrocytes and not shared with neurons or other glial types. Though astrocytes were already regionally patterned in late embryonic stages, this region-specific astrocyte gene expression signature changed dramatically over postnatal development, and its composition suggests that regional astrocytes further specialize postnatally to support their local neuronal circuits. Comparing across species, we found divergence in the expression of astrocytic region- and age-differentially expressed genes and the timing of astrocyte maturation relative to birth between mouse and marmoset, as well as hundreds of species differentially expressed genes. Finally, we used expansion microscopy to show that astrocyte morphology is largely conserved across gray matter forebrain regions in the mouse, despite substantial molecular divergence.

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