A longitudinal two-photon imaging platform for focal astrocyte ablation in vivo
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Investigating the consequences of astrocyte loss in the intact brain is both important and challenging. As integral components of the neuro-glia-vascular unit, astrocytes are involved in a variety of brain processes including water homeostasis, metabolic supply, regulation of cerebral blood flow, and coordination of neuronal circuit activity. Astrocyte impairment has been associated with numerous neurological disorders. However, experimental models combining focal astrocyte ablation with longitudinal in vivo imaging in the intact adult brain have been lacking, limiting efforts to define the causal contribution of astrocyte loss to central nervous system (CNS) pathology and repair.
Here, we present an in vivo model of antibody-mediated astrocyte ablation that enables longitudinal imaging and detailed investigation of ensuing cellular responses. It integrates focal induction of aquaporin-4 antibody-mediated astrocyte loss, chronic in vivo two-photon imaging, genetically encoded sensors, and reporter mouse lines. This advancement allows visualization and quantification of cellular and subcellular events in living organisms during lesion progression and recovery. It overcomes many longstanding limitations of previous models that are either constrained by non-specific hypoxic or mechanical tissue damage or require sacrificing animals at discrete time points, hindering the ability to monitor dynamic biological processes over time. In contrast, the selective targeting of astrocytes prevents the formation of the glial border, enabling the investigation of CNS response in a scar-free environment.
Overall, this new approach represents a significant technical advancement, enabling comprehensive longitudinal studies of CNS responses to astrocyte loss, thus opening new avenues for understanding astrocytopathy-driven pathology, evaluating therapeutic interventions, and promoting translational research.
Significance
Astrocyte loss has been implicated in various neurological disorders, either as a primary cause or as a contributing factor throughout disease progression. However, there remains a critical lack of experimental models capable of directly assessing the impact of astrocyte loss on CNS integrity. Here, we introduce an in vivo model of focal astrocyte ablation that enables multimodal, longitudinal investigation of astrocyte regeneration at both the population and single-cell levels, as well as of dynamic interactions between astrocytes and other CNS cell types. Applications of this model can substantially advance our understanding of the consequences of astrocyte loss in the adult brain, opening new opportunities to investigate its implications in neurological disorders.