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The LRRK2 G2019S mutation alters astrocyte-to-neuron communication via extracellular vesicles and induces neuron atrophy in a human iPSC-derived model of Parkinson’s disease

View ORCID ProfileAurelie de Rus Jacquet, Jenna L. Tancredi, View ORCID ProfileAndrew L. Lemire, View ORCID ProfileMichael C. DeSantis, Wei-Ping Li, View ORCID ProfileErin K. O’Shea
doi: https://doi.org/10.1101/2020.07.02.178574
Aurelie de Rus Jacquet
1Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA, 20147
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  • For correspondence: aureliederus@gmail.com
Jenna L. Tancredi
1Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA, 20147
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Andrew L. Lemire
1Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA, 20147
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Michael C. DeSantis
1Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA, 20147
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Wei-Ping Li
1Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA, 20147
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Erin K. O’Shea
1Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA, 20147
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  • ORCID record for Erin K. O’Shea
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Abstract

Astrocytes are essential cells of the central nervous system, characterized by dynamic relationships with neurons that range from functional metabolic interactions and regulation of neuronal firing activities, to the release of neurotrophic and neuroprotective factors. In Parkinson’s disease (PD), dopaminergic neurons are progressively lost during the course of the disease, but the effects of PD on astrocytes and astrocyte-to-neuron communication remains largely unknown. This study focuses on the effects of the PD-related mutation LRRK2 G2019S in astrocytes generated from patient-derived induced pluripotent stem cells. We report the alteration of extracellular vesicle (EV) biogenesis in astrocytes, and we identify the abnormal accumulation of key PD-related proteins within multi vesicular bodies (MVBs). We found that dopaminergic neurons internalize astrocyte-secreted EVs and that LRRK2 G2019S EVs are abnormally enriched in neurites and fail to provide full neurotrophic support to dopaminergic neurons. Thus, dysfunctional astrocyte-to-neuron communication via altered EV biological properties may participate in the progression of PD.

Competing Interest Statement

Erin K O'Shea: President at the Howard Hughes Medical Institute, one of the three founding funders of eLife.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC 4.0 International license.
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Posted August 13, 2021.
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The LRRK2 G2019S mutation alters astrocyte-to-neuron communication via extracellular vesicles and induces neuron atrophy in a human iPSC-derived model of Parkinson’s disease
Aurelie de Rus Jacquet, Jenna L. Tancredi, Andrew L. Lemire, Michael C. DeSantis, Wei-Ping Li, Erin K. O’Shea
bioRxiv 2020.07.02.178574; doi: https://doi.org/10.1101/2020.07.02.178574
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The LRRK2 G2019S mutation alters astrocyte-to-neuron communication via extracellular vesicles and induces neuron atrophy in a human iPSC-derived model of Parkinson’s disease
Aurelie de Rus Jacquet, Jenna L. Tancredi, Andrew L. Lemire, Michael C. DeSantis, Wei-Ping Li, Erin K. O’Shea
bioRxiv 2020.07.02.178574; doi: https://doi.org/10.1101/2020.07.02.178574

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