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Updated: Jun 13, 2025

Enrichment of Astrocyte-Derived Extracellular Vesicles from Human Plasma
Published on: August 3, 2022
Atypical antipsychotics alter microglial functions via astrocyte-derived extracellular vesicles
Atypical antipsychotics like clozapine and olanzapine impact microglia function indirectly through astrocyte-derived extracellular vesicles (EVs). These EVs modulate microglial phagocytosis and motility, offering potential therapeutic targets for schizophrenia.
Area of Science:
- Neuroscience
- Cell Biology
- Pharmacology
Background:
- Schizophrenia treatment is limited by poor understanding of atypical antipsychotic molecular mechanisms.
- Atypical antipsychotics' effects on non-neuronal cells like astrocytes and microglia are understudied.
- Extracellular vesicles (EVs) from astrocytes are implicated in schizophrenia and may mediate drug effects.
Purpose of the Study:
- To investigate how clozapine and olanzapine affect microglia biology indirectly via astrocyte-derived EVs (ADEVs).
- To determine the impact of ADEVs on microglial phagocytosis, motility, and morphology relevant to schizophrenia.
Main Methods:
- Primary human astrocytes and PBMC-derived microglial-like cells were used in in vitro models.
- Astrocyte-derived EVs (ADEVs) were isolated and applied to microglial cells.
- Microglial phagocytosis of synaptosomes and motility were quantified using image-based methods.
Main Results:
- ADEVs reduced microglial phagocytosis of synaptosomes in a dose-dependent manner.
- This reduction was reversed by ADEVs from astrocytes treated with norclozapine or olanzapine.
- ADEVs from clozapine-treated astrocytes increased microglial motility, altering surveillance activity.
Conclusions:
- Atypical antipsychotics exert distinct, indirect effects on microglia via ADEVs.
- ADEVs play a critical role in glial cell communication.
- ADEVs represent potential therapeutic targets for novel antipsychotic drug development.
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