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Systemic conditioned medium treatment from interleukin-1 primed mesenchymal stem cells promotes recovery after stroke
BACKGROUND: Mesenchymal stem cells (MSCs) hold great potential as a therapy for stroke and have previously been shown to promote recovery in preclinical models of cerebral ischaemia. MSCs secrete a wide range of growth factors, chemokines, cytokines and extracellular vesicles—collectively termed the...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6975095/ https://www.ncbi.nlm.nih.gov/pubmed/31964413 http://dx.doi.org/10.1186/s13287-020-1560-y |
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author | Cunningham, Catriona J. Wong, Raymond Barrington, Jack Tamburrano, Sabrina Pinteaux, Emmanuel Allan, Stuart M. |
author_facet | Cunningham, Catriona J. Wong, Raymond Barrington, Jack Tamburrano, Sabrina Pinteaux, Emmanuel Allan, Stuart M. |
author_sort | Cunningham, Catriona J. |
collection | PubMed |
description | BACKGROUND: Mesenchymal stem cells (MSCs) hold great potential as a therapy for stroke and have previously been shown to promote recovery in preclinical models of cerebral ischaemia. MSCs secrete a wide range of growth factors, chemokines, cytokines and extracellular vesicles—collectively termed the secretome. In this study, we assessed for the first time the efficacy of the IL-1α-primed MSC-derived secretome on brain injury and functional recovery after cerebral ischaemia. METHODS: Stroke was induced in male C57BL/6 mice using the intraluminal filament model of middle cerebral artery occlusion. Conditioned medium from IL-1α-primed MSCs or vehicle was administered at the time of reperfusion or at 24 h post-stroke by subcutaneous injection. RESULTS: IL-1α-primed MSC-derived conditioned medium treatment at the time of stroke led to a ~ 30% reduction in lesion volume at 48 h and was associated with modest improvements in body mass gain, 28-point neurological score and nest building. Administration of MSC-derived conditioned medium at 24 h post-stroke led to improved nest building and neurological score despite no observed differences in lesion volume at day 2 post-stroke. CONCLUSIONS: Our results show for the first time that the administration of conditioned medium from IL-1α-primed MSCs leads to improvements in behavioural outcomes independently of neuroprotection. |
format | Online Article Text |
id | pubmed-6975095 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-69750952020-01-28 Systemic conditioned medium treatment from interleukin-1 primed mesenchymal stem cells promotes recovery after stroke Cunningham, Catriona J. Wong, Raymond Barrington, Jack Tamburrano, Sabrina Pinteaux, Emmanuel Allan, Stuart M. Stem Cell Res Ther Research BACKGROUND: Mesenchymal stem cells (MSCs) hold great potential as a therapy for stroke and have previously been shown to promote recovery in preclinical models of cerebral ischaemia. MSCs secrete a wide range of growth factors, chemokines, cytokines and extracellular vesicles—collectively termed the secretome. In this study, we assessed for the first time the efficacy of the IL-1α-primed MSC-derived secretome on brain injury and functional recovery after cerebral ischaemia. METHODS: Stroke was induced in male C57BL/6 mice using the intraluminal filament model of middle cerebral artery occlusion. Conditioned medium from IL-1α-primed MSCs or vehicle was administered at the time of reperfusion or at 24 h post-stroke by subcutaneous injection. RESULTS: IL-1α-primed MSC-derived conditioned medium treatment at the time of stroke led to a ~ 30% reduction in lesion volume at 48 h and was associated with modest improvements in body mass gain, 28-point neurological score and nest building. Administration of MSC-derived conditioned medium at 24 h post-stroke led to improved nest building and neurological score despite no observed differences in lesion volume at day 2 post-stroke. CONCLUSIONS: Our results show for the first time that the administration of conditioned medium from IL-1α-primed MSCs leads to improvements in behavioural outcomes independently of neuroprotection. BioMed Central 2020-01-21 /pmc/articles/PMC6975095/ /pubmed/31964413 http://dx.doi.org/10.1186/s13287-020-1560-y Text en © The Author(s). 2020 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Cunningham, Catriona J. Wong, Raymond Barrington, Jack Tamburrano, Sabrina Pinteaux, Emmanuel Allan, Stuart M. Systemic conditioned medium treatment from interleukin-1 primed mesenchymal stem cells promotes recovery after stroke |
title | Systemic conditioned medium treatment from interleukin-1 primed mesenchymal stem cells promotes recovery after stroke |
title_full | Systemic conditioned medium treatment from interleukin-1 primed mesenchymal stem cells promotes recovery after stroke |
title_fullStr | Systemic conditioned medium treatment from interleukin-1 primed mesenchymal stem cells promotes recovery after stroke |
title_full_unstemmed | Systemic conditioned medium treatment from interleukin-1 primed mesenchymal stem cells promotes recovery after stroke |
title_short | Systemic conditioned medium treatment from interleukin-1 primed mesenchymal stem cells promotes recovery after stroke |
title_sort | systemic conditioned medium treatment from interleukin-1 primed mesenchymal stem cells promotes recovery after stroke |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6975095/ https://www.ncbi.nlm.nih.gov/pubmed/31964413 http://dx.doi.org/10.1186/s13287-020-1560-y |
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