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Combination of human endothelial colony-forming cells and mesenchymal stromal cells exert neuroprotective effects in the growth-restricted newborn

The foetal brain is particularly vulnerable to the detrimental effects of foetal growth restriction (FGR) with subsequent abnormal neurodevelopment being common. There are no current treatments to protect the FGR newborn from lifelong neurological disorders. This study examines whether pure foetal m...

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Autores principales: Chand, Kirat K., Patel, Jatin, Bjorkman, S. T., Sim, Seen-Ling, Miller, Stephanie M., Teo, Elliot, Jones, Lara, Sun, Jane, Colditz, Paul B., Khosrotehrani, Kiarash, Wixey, Julie A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8602245/
https://www.ncbi.nlm.nih.gov/pubmed/34795316
http://dx.doi.org/10.1038/s41536-021-00185-5
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author Chand, Kirat K.
Patel, Jatin
Bjorkman, S. T.
Sim, Seen-Ling
Miller, Stephanie M.
Teo, Elliot
Jones, Lara
Sun, Jane
Colditz, Paul B.
Khosrotehrani, Kiarash
Wixey, Julie A.
author_facet Chand, Kirat K.
Patel, Jatin
Bjorkman, S. T.
Sim, Seen-Ling
Miller, Stephanie M.
Teo, Elliot
Jones, Lara
Sun, Jane
Colditz, Paul B.
Khosrotehrani, Kiarash
Wixey, Julie A.
author_sort Chand, Kirat K.
collection PubMed
description The foetal brain is particularly vulnerable to the detrimental effects of foetal growth restriction (FGR) with subsequent abnormal neurodevelopment being common. There are no current treatments to protect the FGR newborn from lifelong neurological disorders. This study examines whether pure foetal mesenchymal stromal cells (MSC) and endothelial colony-forming cells (ECFC) from the human term placenta are neuroprotective through modulating neuroinflammation and supporting the brain vasculature. We determined that one dose of combined MSC-ECFCs (cECFC; 10(6) ECFC 10(6) MSC) on the first day of life to the newborn FGR piglet improved damaged vasculature, restored the neurovascular unit, reduced brain inflammation and improved adverse neuronal and white matter changes present in the FGR newborn piglet brain. These findings could not be reproduced using MSCs alone. These results demonstrate cECFC treatment exerts beneficial effects on multiple cellular components in the FGR brain and may act as a neuroprotectant.
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spelling pubmed-86022452021-11-19 Combination of human endothelial colony-forming cells and mesenchymal stromal cells exert neuroprotective effects in the growth-restricted newborn Chand, Kirat K. Patel, Jatin Bjorkman, S. T. Sim, Seen-Ling Miller, Stephanie M. Teo, Elliot Jones, Lara Sun, Jane Colditz, Paul B. Khosrotehrani, Kiarash Wixey, Julie A. NPJ Regen Med Article The foetal brain is particularly vulnerable to the detrimental effects of foetal growth restriction (FGR) with subsequent abnormal neurodevelopment being common. There are no current treatments to protect the FGR newborn from lifelong neurological disorders. This study examines whether pure foetal mesenchymal stromal cells (MSC) and endothelial colony-forming cells (ECFC) from the human term placenta are neuroprotective through modulating neuroinflammation and supporting the brain vasculature. We determined that one dose of combined MSC-ECFCs (cECFC; 10(6) ECFC 10(6) MSC) on the first day of life to the newborn FGR piglet improved damaged vasculature, restored the neurovascular unit, reduced brain inflammation and improved adverse neuronal and white matter changes present in the FGR newborn piglet brain. These findings could not be reproduced using MSCs alone. These results demonstrate cECFC treatment exerts beneficial effects on multiple cellular components in the FGR brain and may act as a neuroprotectant. Nature Publishing Group UK 2021-11-18 /pmc/articles/PMC8602245/ /pubmed/34795316 http://dx.doi.org/10.1038/s41536-021-00185-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Chand, Kirat K.
Patel, Jatin
Bjorkman, S. T.
Sim, Seen-Ling
Miller, Stephanie M.
Teo, Elliot
Jones, Lara
Sun, Jane
Colditz, Paul B.
Khosrotehrani, Kiarash
Wixey, Julie A.
Combination of human endothelial colony-forming cells and mesenchymal stromal cells exert neuroprotective effects in the growth-restricted newborn
title Combination of human endothelial colony-forming cells and mesenchymal stromal cells exert neuroprotective effects in the growth-restricted newborn
title_full Combination of human endothelial colony-forming cells and mesenchymal stromal cells exert neuroprotective effects in the growth-restricted newborn
title_fullStr Combination of human endothelial colony-forming cells and mesenchymal stromal cells exert neuroprotective effects in the growth-restricted newborn
title_full_unstemmed Combination of human endothelial colony-forming cells and mesenchymal stromal cells exert neuroprotective effects in the growth-restricted newborn
title_short Combination of human endothelial colony-forming cells and mesenchymal stromal cells exert neuroprotective effects in the growth-restricted newborn
title_sort combination of human endothelial colony-forming cells and mesenchymal stromal cells exert neuroprotective effects in the growth-restricted newborn
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8602245/
https://www.ncbi.nlm.nih.gov/pubmed/34795316
http://dx.doi.org/10.1038/s41536-021-00185-5
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