Human iPSC-derived astrocytes transplanted into the mouse brain undergo morphological changes in response to amyloid-β plaques

Background Increasing evidence for a direct contribution of astrocytes to neuroinflammatory and neurodegenerative processes causing Alzheimer's disease comes from molecular and functional studies in rodent models. However, these models may not fully recapitulate human disease as human and rodent astrocytes differ considerably in morphology, functionality, and gene expression. Results To address these challenges, we established an approach to study human astrocytes within the mouse brain by transplanting human induced pluripotent stem cell (hiPSC)-derived astrocyte progenitors into neonatal brains. Xenografted hiPSC-derived astrocyte progenitors differentiated into astrocytes that integrated functionally within the mouse host brain and matured in a cell-autonomous way retaining human-specific morphologies, unique features, and physiological properties. In Alzheimer ' s chimeric brains, transplanted hiPSC-derived astrocytes responded to the presence of amyloid plaques undergoing morphological changes that seemed independent of the APOE allelic background. Conclusions In sum, we describe here a promising approach that consist of transplanting patient-derived and genetically modified astrocytes into the mouse brain to study human astrocyte pathophysiology in the context of Alzheimer ' s disease.

Automated summary

Transplanting human induced pluripotent stem cell (hiPSC)-derived astrocyte progenitors into the mouse brain offers a promising approach to study human astrocyte pathophysiology in the context of Alzheimer's disease. The transplanted astrocytes develop and integrate functionally within the mouse host brain, maintaining human-specific characteristics and responses to amyloid plaques in Alzheimer's chimeric brains. This method provides valuable insights into the differences between human and rodent astrocytes and their role in neuroinflammatory and neurodegenerative processes.