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Therapeutic role of mesenchymal stem cell‐derived extracellular vesicles in neuroinflammation and cognitive dysfunctions induced by binge‐like ethanol treatment in adolescent mice

BACKGROUND: Extracellular vesicles (EVs) are heterogeneous membrane vesicles secreted by cells in extracellular spaces that play an important role in intercellular communication under both normal and pathological conditions. Mesenchymal stem cells (MSC) are anti‐inflammatory and immunoregulatory cel...

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Autores principales: Mellado, Susana, Cuesta, Carlos M., Montagud, Sandra, Rodríguez‐Arias, Marta, Moreno‐Manzano, Victoria, Guerri, Consuelo, Pascual, María
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10651955/
https://www.ncbi.nlm.nih.gov/pubmed/37381698
http://dx.doi.org/10.1111/cns.14326
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author Mellado, Susana
Cuesta, Carlos M.
Montagud, Sandra
Rodríguez‐Arias, Marta
Moreno‐Manzano, Victoria
Guerri, Consuelo
Pascual, María
author_facet Mellado, Susana
Cuesta, Carlos M.
Montagud, Sandra
Rodríguez‐Arias, Marta
Moreno‐Manzano, Victoria
Guerri, Consuelo
Pascual, María
author_sort Mellado, Susana
collection PubMed
description BACKGROUND: Extracellular vesicles (EVs) are heterogeneous membrane vesicles secreted by cells in extracellular spaces that play an important role in intercellular communication under both normal and pathological conditions. Mesenchymal stem cells (MSC) are anti‐inflammatory and immunoregulatory cells capable of secreting EVs, which are considered promising molecules for treating immune, inflammatory, and degenerative diseases. Our previous studies demonstrate that, by activating innate immune receptors TLR4 (Toll‐like receptor 4), binge‐like ethanol exposure in adolescence causes neuroinflammation and neural damage. AIMS: To evaluate whether the intravenous administration of MSC‐derived EVs is capable of reducing neuroinflammation, myelin and synaptic alterations, and the cognitive dysfunction induced by binge‐like ethanol treatment in adolescent mice. MATERIALS & METHODS: MSC–derived EVs obtained from adipose tissue were administered in the tail vein (50 microg/dose, one weekly dose) to female WT adolescent mice treated intermittently with ethanol (3.0 g/kg) during two weeks. RESULTS: MSC‐derived EVs from adipose tissue ameliorate ethanol‐induced up‐regulation of inflammatory genes (e.g., COX‐2, iNOS, MIP‐1α, NF‐κB, CX3CL1, and MCP‐1) in the prefrontal cortex of adolescent mice. Notably, MSC‐derived EVs also restore the myelin and synaptic derangements, and the memory and learning impairments, induced by ethanol treatment. Using cortical astroglial cells in culture, our results further confirm that MSC‐derived EVs decrease inflammatory genes in ethanol‐treated astroglial cells. This, in turn, confirms in vivo findings. CONCLUSION: Taken together, these results provide the first evidence for the therapeutic potential of the MSC‐derived EVs in the neuroimmune response and cognitive dysfunction induced by binge alcohol drinking in adolescence.
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spelling pubmed-106519552023-06-28 Therapeutic role of mesenchymal stem cell‐derived extracellular vesicles in neuroinflammation and cognitive dysfunctions induced by binge‐like ethanol treatment in adolescent mice Mellado, Susana Cuesta, Carlos M. Montagud, Sandra Rodríguez‐Arias, Marta Moreno‐Manzano, Victoria Guerri, Consuelo Pascual, María CNS Neurosci Ther Original Articles BACKGROUND: Extracellular vesicles (EVs) are heterogeneous membrane vesicles secreted by cells in extracellular spaces that play an important role in intercellular communication under both normal and pathological conditions. Mesenchymal stem cells (MSC) are anti‐inflammatory and immunoregulatory cells capable of secreting EVs, which are considered promising molecules for treating immune, inflammatory, and degenerative diseases. Our previous studies demonstrate that, by activating innate immune receptors TLR4 (Toll‐like receptor 4), binge‐like ethanol exposure in adolescence causes neuroinflammation and neural damage. AIMS: To evaluate whether the intravenous administration of MSC‐derived EVs is capable of reducing neuroinflammation, myelin and synaptic alterations, and the cognitive dysfunction induced by binge‐like ethanol treatment in adolescent mice. MATERIALS & METHODS: MSC–derived EVs obtained from adipose tissue were administered in the tail vein (50 microg/dose, one weekly dose) to female WT adolescent mice treated intermittently with ethanol (3.0 g/kg) during two weeks. RESULTS: MSC‐derived EVs from adipose tissue ameliorate ethanol‐induced up‐regulation of inflammatory genes (e.g., COX‐2, iNOS, MIP‐1α, NF‐κB, CX3CL1, and MCP‐1) in the prefrontal cortex of adolescent mice. Notably, MSC‐derived EVs also restore the myelin and synaptic derangements, and the memory and learning impairments, induced by ethanol treatment. Using cortical astroglial cells in culture, our results further confirm that MSC‐derived EVs decrease inflammatory genes in ethanol‐treated astroglial cells. This, in turn, confirms in vivo findings. CONCLUSION: Taken together, these results provide the first evidence for the therapeutic potential of the MSC‐derived EVs in the neuroimmune response and cognitive dysfunction induced by binge alcohol drinking in adolescence. John Wiley and Sons Inc. 2023-06-28 /pmc/articles/PMC10651955/ /pubmed/37381698 http://dx.doi.org/10.1111/cns.14326 Text en © 2023 The Authors. CNS Neuroscience & Therapeutics published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Mellado, Susana
Cuesta, Carlos M.
Montagud, Sandra
Rodríguez‐Arias, Marta
Moreno‐Manzano, Victoria
Guerri, Consuelo
Pascual, María
Therapeutic role of mesenchymal stem cell‐derived extracellular vesicles in neuroinflammation and cognitive dysfunctions induced by binge‐like ethanol treatment in adolescent mice
title Therapeutic role of mesenchymal stem cell‐derived extracellular vesicles in neuroinflammation and cognitive dysfunctions induced by binge‐like ethanol treatment in adolescent mice
title_full Therapeutic role of mesenchymal stem cell‐derived extracellular vesicles in neuroinflammation and cognitive dysfunctions induced by binge‐like ethanol treatment in adolescent mice
title_fullStr Therapeutic role of mesenchymal stem cell‐derived extracellular vesicles in neuroinflammation and cognitive dysfunctions induced by binge‐like ethanol treatment in adolescent mice
title_full_unstemmed Therapeutic role of mesenchymal stem cell‐derived extracellular vesicles in neuroinflammation and cognitive dysfunctions induced by binge‐like ethanol treatment in adolescent mice
title_short Therapeutic role of mesenchymal stem cell‐derived extracellular vesicles in neuroinflammation and cognitive dysfunctions induced by binge‐like ethanol treatment in adolescent mice
title_sort therapeutic role of mesenchymal stem cell‐derived extracellular vesicles in neuroinflammation and cognitive dysfunctions induced by binge‐like ethanol treatment in adolescent mice
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10651955/
https://www.ncbi.nlm.nih.gov/pubmed/37381698
http://dx.doi.org/10.1111/cns.14326
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