AstroGreen transgenic mouse illuminates the trafficking of astrocyte-derived extracellular vesicles

Astrocytes interact with neighboring cells by releasing extracellular vesicles (EVs). Tools to study astrocyte EV-mediated communication with other brain cells in vivo are essential. In this study, we crossed the Exomap1 transgenic mouse expressing Cre-activated human-specific CD81 (HsCD81) fused to the fluorescent protein mNeonGreen (HsCD81mNG), to a transgenic mouse expressing Cre under the astrocyte-expressing GFAP promoter resulting in Exomap1::Gfap-Cre mice, referred to here as AstroGreen. We characterized HsCD81mNG-expressing astrocytes and shedded EVs loaded with HsCD81mNG and Cre, both in vitro and in mouse brains. Using this model, we show that HsCD81mNG can be used to track EV content, production, and functional Cre transfer in vitro and in the brain, allowing evaluation of the interaction of astrocytes with neighboring cells mediated by EVs. We anticipate that this model will improve our understanding of astrocytes transferring EVs within their surroundings during normal physiological processes and in the context of neuropathological conditions.

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Publication Details

Journal
Molecular and Cellular Neuroscience
Published
2025-10-09
DOI
https://doi.org/10.1016/j.mcn.2025.104051
Primary Topic
Extracellular vesicles in disease
Type
article
Field-Weighted Citation Impact
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article

AstroGreen transgenic mouse illuminates the trafficking of astrocyte-derived extracellular vesicles

Erik R. Abels, David Rufino‐Ramos, Edwina Abou Haidar, Saumya Das et al.
Molecular and Cellular Neuroscience
Extracellular vesicles in disease
article

AstroGreen transgenic mouse illuminates the trafficking of astrocyte-derived extracellular vesicles

Erik R. Abels, David Rufino‐Ramos, Edwina Abou Haidar, Saumya Das, Stephen J. Gould, Shilpa Prabhakar, Francis K. Fordjour, Koen Breyne, Marike L. D. Broekman, Lisa Nieland, Youssef Samaha, Xandra O. Breakefield
article en

Abstract

Astrocytes interact with neighboring cells by releasing extracellular vesicles (EVs). Tools to study astrocyte EV-mediated communication with other brain cells in vivo are essential. In this study, we crossed the Exomap1 transgenic mouse expressing Cre-activated human-specific CD81 (HsCD81) fused to the fluorescent protein mNeonGreen (HsCD81mNG), to a transgenic mouse expressing Cre under the astrocyte-expressing GFAP promoter resulting in Exomap1::Gfap-Cre mice, referred to here as AstroGreen. We characterized HsCD81mNG-expressing astrocytes and shedded EVs loaded with HsCD81mNG and Cre, both in vitro and in mouse brains. Using this model, we show that HsCD81mNG can be used to track EV content, production, and functional Cre transfer in vitro and in the brain, allowing evaluation of the interaction of astrocytes with neighboring cells mediated by EVs. We anticipate that this model will improve our understanding of astrocytes transferring EVs within their surroundings during normal physiological processes and in the context of neuropathological conditions.

Molecular and Cellular NeuroscienceVol. 135
Harvard University (US), Johns Hopkins University (US), Johns Hopkins Medicine (US), Leiden University Medical Center (NL), Massachusetts General Hospital (US), Center for Systems Biology (US)
Openalex Percentile: Top 75%
Extracellular vesicles in disease
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