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Neuroprotection mediated by cystatin C-loaded extracellular vesicles

Cystatin C (CysC) is implicated in neuroprotection and repair in the nervous system in response to diverse neurotoxic conditions. In addition to being secreted from cells in a soluble form, CysC is released by cells in association with extracellular vesicles (EVs), including exosomes. We demonstrate...

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Autores principales: Pérez-González, Rocío, Sahoo, Susmita, Gauthier, Sebastien A., Kim, Yohan, Li, Meihua, Kumar, Asok, Pawlik, Monika, Benussi, Luisa, Ghidoni, Roberta, Levy, Efrat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6668451/
https://www.ncbi.nlm.nih.gov/pubmed/31367000
http://dx.doi.org/10.1038/s41598-019-47524-7
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author Pérez-González, Rocío
Sahoo, Susmita
Gauthier, Sebastien A.
Kim, Yohan
Li, Meihua
Kumar, Asok
Pawlik, Monika
Benussi, Luisa
Ghidoni, Roberta
Levy, Efrat
author_facet Pérez-González, Rocío
Sahoo, Susmita
Gauthier, Sebastien A.
Kim, Yohan
Li, Meihua
Kumar, Asok
Pawlik, Monika
Benussi, Luisa
Ghidoni, Roberta
Levy, Efrat
author_sort Pérez-González, Rocío
collection PubMed
description Cystatin C (CysC) is implicated in neuroprotection and repair in the nervous system in response to diverse neurotoxic conditions. In addition to being secreted from cells in a soluble form, CysC is released by cells in association with extracellular vesicles (EVs), including exosomes. We demonstrate that EVs containing CysC protect cultured cells from starvation-induced death. Moreover, while EVs secreted by CysC-deficient cells were not protective, EVs secreted by CysC-deficient cells treated with exogenous human CysC significantly enhanced the survival of the cells. CysC also plays a role in modulating the secretion of EVs, enhancing secretion of EVs by primary cortical neurons and primary cortical smooth muscle cells. Confirming these in vitro findings, higher EV levels were observed in the brain extracellular space of transgenic mice expressing human CysC as compared to littermate controls. Regulation of cell-secreted EV levels and content in the brain is likely to be essential to maintaining normal brain function. We propose that enhanced EV release could rescue the deleterious effects of dysfunction of the endosomal-lysosomal system in neurodegenerative disorders. Moreover, a higher level of CysC-loaded EVs released from cells in the central nervous system has important protective functions, representing a potential therapeutic tool for disorders of the central nervous system.
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spelling pubmed-66684512019-08-06 Neuroprotection mediated by cystatin C-loaded extracellular vesicles Pérez-González, Rocío Sahoo, Susmita Gauthier, Sebastien A. Kim, Yohan Li, Meihua Kumar, Asok Pawlik, Monika Benussi, Luisa Ghidoni, Roberta Levy, Efrat Sci Rep Article Cystatin C (CysC) is implicated in neuroprotection and repair in the nervous system in response to diverse neurotoxic conditions. In addition to being secreted from cells in a soluble form, CysC is released by cells in association with extracellular vesicles (EVs), including exosomes. We demonstrate that EVs containing CysC protect cultured cells from starvation-induced death. Moreover, while EVs secreted by CysC-deficient cells were not protective, EVs secreted by CysC-deficient cells treated with exogenous human CysC significantly enhanced the survival of the cells. CysC also plays a role in modulating the secretion of EVs, enhancing secretion of EVs by primary cortical neurons and primary cortical smooth muscle cells. Confirming these in vitro findings, higher EV levels were observed in the brain extracellular space of transgenic mice expressing human CysC as compared to littermate controls. Regulation of cell-secreted EV levels and content in the brain is likely to be essential to maintaining normal brain function. We propose that enhanced EV release could rescue the deleterious effects of dysfunction of the endosomal-lysosomal system in neurodegenerative disorders. Moreover, a higher level of CysC-loaded EVs released from cells in the central nervous system has important protective functions, representing a potential therapeutic tool for disorders of the central nervous system. Nature Publishing Group UK 2019-07-31 /pmc/articles/PMC6668451/ /pubmed/31367000 http://dx.doi.org/10.1038/s41598-019-47524-7 Text en © The Author(s) 2019 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Pérez-González, Rocío
Sahoo, Susmita
Gauthier, Sebastien A.
Kim, Yohan
Li, Meihua
Kumar, Asok
Pawlik, Monika
Benussi, Luisa
Ghidoni, Roberta
Levy, Efrat
Neuroprotection mediated by cystatin C-loaded extracellular vesicles
title Neuroprotection mediated by cystatin C-loaded extracellular vesicles
title_full Neuroprotection mediated by cystatin C-loaded extracellular vesicles
title_fullStr Neuroprotection mediated by cystatin C-loaded extracellular vesicles
title_full_unstemmed Neuroprotection mediated by cystatin C-loaded extracellular vesicles
title_short Neuroprotection mediated by cystatin C-loaded extracellular vesicles
title_sort neuroprotection mediated by cystatin c-loaded extracellular vesicles
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6668451/
https://www.ncbi.nlm.nih.gov/pubmed/31367000
http://dx.doi.org/10.1038/s41598-019-47524-7
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