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Cocaine Modulates the Neuronal Endosomal System and Extracellular Vesicles in a Sex-Dependent Manner
In multiple neurodevelopmental and neurodegenerative disorders, endosomal changes correlate with changes in exosomes. We examined this linkage in the brain of mice that received cocaine injections for two weeks starting at 2.5 months of age. Cocaine caused a decrease in the number of both neuronal e...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9352616/ https://www.ncbi.nlm.nih.gov/pubmed/35501523 http://dx.doi.org/10.1007/s11064-022-03612-1 |
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author | Barreto, Bryana R. D’Acunzo, Pasquale Ungania, Jonathan M. Das, Sasmita Hashim, Audrey Goulbourne, Chris N. Canals-Baker, Stefanie Saito, Mitsuo Saito, Mariko Sershen, Henry Levy, Efrat |
author_facet | Barreto, Bryana R. D’Acunzo, Pasquale Ungania, Jonathan M. Das, Sasmita Hashim, Audrey Goulbourne, Chris N. Canals-Baker, Stefanie Saito, Mitsuo Saito, Mariko Sershen, Henry Levy, Efrat |
author_sort | Barreto, Bryana R. |
collection | PubMed |
description | In multiple neurodevelopmental and neurodegenerative disorders, endosomal changes correlate with changes in exosomes. We examined this linkage in the brain of mice that received cocaine injections for two weeks starting at 2.5 months of age. Cocaine caused a decrease in the number of both neuronal early and late endosomes and exosomes in the brains of male but not female mice. The response to cocaine in ovariectomized females mirrored male, demonstrating that these sex-differences in response to cocaine are driven by hormonal differences. Moreover, cocaine increased the amount of α-synuclein per exosome in the brain of females but did not affect exosomal α-synuclein content in the brain of males, a sex-difference eliminated by ovariectomy. Enhanced packaging of α-synuclein into female brain exosomes with the potential for propagation of pathology throughout the brain suggests a mechanism for the different response of females to chronic cocaine exposure as compared to males. |
format | Online Article Text |
id | pubmed-9352616 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-93526162022-08-06 Cocaine Modulates the Neuronal Endosomal System and Extracellular Vesicles in a Sex-Dependent Manner Barreto, Bryana R. D’Acunzo, Pasquale Ungania, Jonathan M. Das, Sasmita Hashim, Audrey Goulbourne, Chris N. Canals-Baker, Stefanie Saito, Mitsuo Saito, Mariko Sershen, Henry Levy, Efrat Neurochem Res Original Paper In multiple neurodevelopmental and neurodegenerative disorders, endosomal changes correlate with changes in exosomes. We examined this linkage in the brain of mice that received cocaine injections for two weeks starting at 2.5 months of age. Cocaine caused a decrease in the number of both neuronal early and late endosomes and exosomes in the brains of male but not female mice. The response to cocaine in ovariectomized females mirrored male, demonstrating that these sex-differences in response to cocaine are driven by hormonal differences. Moreover, cocaine increased the amount of α-synuclein per exosome in the brain of females but did not affect exosomal α-synuclein content in the brain of males, a sex-difference eliminated by ovariectomy. Enhanced packaging of α-synuclein into female brain exosomes with the potential for propagation of pathology throughout the brain suggests a mechanism for the different response of females to chronic cocaine exposure as compared to males. Springer US 2022-04-30 2022 /pmc/articles/PMC9352616/ /pubmed/35501523 http://dx.doi.org/10.1007/s11064-022-03612-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Paper Barreto, Bryana R. D’Acunzo, Pasquale Ungania, Jonathan M. Das, Sasmita Hashim, Audrey Goulbourne, Chris N. Canals-Baker, Stefanie Saito, Mitsuo Saito, Mariko Sershen, Henry Levy, Efrat Cocaine Modulates the Neuronal Endosomal System and Extracellular Vesicles in a Sex-Dependent Manner |
title | Cocaine Modulates the Neuronal Endosomal System and Extracellular Vesicles in a Sex-Dependent Manner |
title_full | Cocaine Modulates the Neuronal Endosomal System and Extracellular Vesicles in a Sex-Dependent Manner |
title_fullStr | Cocaine Modulates the Neuronal Endosomal System and Extracellular Vesicles in a Sex-Dependent Manner |
title_full_unstemmed | Cocaine Modulates the Neuronal Endosomal System and Extracellular Vesicles in a Sex-Dependent Manner |
title_short | Cocaine Modulates the Neuronal Endosomal System and Extracellular Vesicles in a Sex-Dependent Manner |
title_sort | cocaine modulates the neuronal endosomal system and extracellular vesicles in a sex-dependent manner |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9352616/ https://www.ncbi.nlm.nih.gov/pubmed/35501523 http://dx.doi.org/10.1007/s11064-022-03612-1 |
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