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Mesenchymal stromal cell derived extracellular vesicles rescue radiation damage to murine marrow hematopoietic cells
Mesenchymal stromal cells (MSC) have been shown to reverse radiation damage to marrow stem cells. We have evaluated the capacity of MSC-derived extracellular vesicles (MSC-EVs) to mitigate radiation injury to marrow stem cells at 4 hours to 7 days after irradiation. Significant restoration of marrow...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5093052/ https://www.ncbi.nlm.nih.gov/pubmed/27150009 http://dx.doi.org/10.1038/leu.2016.107 |
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author | Wen, Sicheng Dooner, Mark Cheng, Yan Papa, Elaine Del Tatto, Michael Pereira, Mandy Deng, Yanhui Goldberg, Laura Aliotta, Jason Chatterjee, Devasis Stewart, Connor Carpanetto, Andrea Collino, Federica Bruno, Stefania Camussi, Giovanni Quesenberry, Peter |
author_facet | Wen, Sicheng Dooner, Mark Cheng, Yan Papa, Elaine Del Tatto, Michael Pereira, Mandy Deng, Yanhui Goldberg, Laura Aliotta, Jason Chatterjee, Devasis Stewart, Connor Carpanetto, Andrea Collino, Federica Bruno, Stefania Camussi, Giovanni Quesenberry, Peter |
author_sort | Wen, Sicheng |
collection | PubMed |
description | Mesenchymal stromal cells (MSC) have been shown to reverse radiation damage to marrow stem cells. We have evaluated the capacity of MSC-derived extracellular vesicles (MSC-EVs) to mitigate radiation injury to marrow stem cells at 4 hours to 7 days after irradiation. Significant restoration of marrow stem cell engraftment at 4, 24 and 168 hours post-irradiation by exposure to MSC-EVs was observed at 3 weeks to 9 months after transplant and further confirmed by secondary engraftment. Intravenous injection of MSC-EVs to 500cGy exposed mice led to partial recovery of peripheral blood counts and restoration of the engraftment of marrow. The murine hematopoietic cell line, FDC-P1 exposed to 500 cGy, showed reversal of growth inhibition, DNA damage and apoptosis on exposure to murine or human MSC-EVs. Both murine and human MSC-EVs reverse radiation damage to murine marrow cells and stimulate normal murine marrow stem cell/progenitors to proliferate. A preparation with both exosomes and microvesicles was found to be superior to either microvesicles or exosomes alone. Biologic activity was seen in freshly isolated vesicles and in vesicles stored for up to 6 months in 10% DMSO at −80°C. These studies indicate that MSC-EVs can reverse radiation damage to bone marrow stem cells. |
format | Online Article Text |
id | pubmed-5093052 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
record_format | MEDLINE/PubMed |
spelling | pubmed-50930522016-11-06 Mesenchymal stromal cell derived extracellular vesicles rescue radiation damage to murine marrow hematopoietic cells Wen, Sicheng Dooner, Mark Cheng, Yan Papa, Elaine Del Tatto, Michael Pereira, Mandy Deng, Yanhui Goldberg, Laura Aliotta, Jason Chatterjee, Devasis Stewart, Connor Carpanetto, Andrea Collino, Federica Bruno, Stefania Camussi, Giovanni Quesenberry, Peter Leukemia Article Mesenchymal stromal cells (MSC) have been shown to reverse radiation damage to marrow stem cells. We have evaluated the capacity of MSC-derived extracellular vesicles (MSC-EVs) to mitigate radiation injury to marrow stem cells at 4 hours to 7 days after irradiation. Significant restoration of marrow stem cell engraftment at 4, 24 and 168 hours post-irradiation by exposure to MSC-EVs was observed at 3 weeks to 9 months after transplant and further confirmed by secondary engraftment. Intravenous injection of MSC-EVs to 500cGy exposed mice led to partial recovery of peripheral blood counts and restoration of the engraftment of marrow. The murine hematopoietic cell line, FDC-P1 exposed to 500 cGy, showed reversal of growth inhibition, DNA damage and apoptosis on exposure to murine or human MSC-EVs. Both murine and human MSC-EVs reverse radiation damage to murine marrow cells and stimulate normal murine marrow stem cell/progenitors to proliferate. A preparation with both exosomes and microvesicles was found to be superior to either microvesicles or exosomes alone. Biologic activity was seen in freshly isolated vesicles and in vesicles stored for up to 6 months in 10% DMSO at −80°C. These studies indicate that MSC-EVs can reverse radiation damage to bone marrow stem cells. 2016-05-06 2016-11 /pmc/articles/PMC5093052/ /pubmed/27150009 http://dx.doi.org/10.1038/leu.2016.107 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Wen, Sicheng Dooner, Mark Cheng, Yan Papa, Elaine Del Tatto, Michael Pereira, Mandy Deng, Yanhui Goldberg, Laura Aliotta, Jason Chatterjee, Devasis Stewart, Connor Carpanetto, Andrea Collino, Federica Bruno, Stefania Camussi, Giovanni Quesenberry, Peter Mesenchymal stromal cell derived extracellular vesicles rescue radiation damage to murine marrow hematopoietic cells |
title | Mesenchymal stromal cell derived extracellular vesicles rescue radiation damage to murine marrow hematopoietic cells |
title_full | Mesenchymal stromal cell derived extracellular vesicles rescue radiation damage to murine marrow hematopoietic cells |
title_fullStr | Mesenchymal stromal cell derived extracellular vesicles rescue radiation damage to murine marrow hematopoietic cells |
title_full_unstemmed | Mesenchymal stromal cell derived extracellular vesicles rescue radiation damage to murine marrow hematopoietic cells |
title_short | Mesenchymal stromal cell derived extracellular vesicles rescue radiation damage to murine marrow hematopoietic cells |
title_sort | mesenchymal stromal cell derived extracellular vesicles rescue radiation damage to murine marrow hematopoietic cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5093052/ https://www.ncbi.nlm.nih.gov/pubmed/27150009 http://dx.doi.org/10.1038/leu.2016.107 |
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