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Exosomes of human placenta-derived mesenchymal stem cells stimulate angiogenesis
BACKGROUND: The therapeutic potential of mesenchymal stem cells (MSCs) may be attributed partly to humoral factors such as growth factors, cytokines, and chemokines. Human term placental tissue-derived MSCs (PlaMSCs), or conditioned medium left over from cultures of these cells, have been reported t...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5627451/ https://www.ncbi.nlm.nih.gov/pubmed/28974256 http://dx.doi.org/10.1186/s13287-017-0660-9 |
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author | Komaki, Motohiro Numata, Yuri Morioka, Chikako Honda, Izumi Tooi, Masayuki Yokoyama, Naoki Ayame, Hirohito Iwasaki, Kengo Taki, Atsuko Oshima, Noriko Morita, Ikuo |
author_facet | Komaki, Motohiro Numata, Yuri Morioka, Chikako Honda, Izumi Tooi, Masayuki Yokoyama, Naoki Ayame, Hirohito Iwasaki, Kengo Taki, Atsuko Oshima, Noriko Morita, Ikuo |
author_sort | Komaki, Motohiro |
collection | PubMed |
description | BACKGROUND: The therapeutic potential of mesenchymal stem cells (MSCs) may be attributed partly to humoral factors such as growth factors, cytokines, and chemokines. Human term placental tissue-derived MSCs (PlaMSCs), or conditioned medium left over from cultures of these cells, have been reported to enhance angiogenesis. Recently, the exosome, which can transport a diverse suite of macromolecules, has gained attention as a novel intercellular communication tool. However, the potential role of the exosome in PlaMSC therapeutic action is not well understood. The purpose of this study was to evaluate PlaMSC-derived exosome angiogenesis promotion in vitro and in vivo. METHODS: MSCs were isolated from human term placental tissue by enzymatic digestion. Conditioned medium was collected after 48-h incubation in serum-free medium (PlaMSC-CM). Angiogenic factors present in PlaMSC-CM were screened by a growth factor array. Exosomes were prepared by ultracentrifugation of PlaMSC-CM, and confirmed by transmission electron microscopy, dynamic light scattering, and western blot analyses. The proangiogenic activity of PlaMSC-derived exosomes (PlaMSC-exo) was assessed using an endothelial tube formation assay, a cell migration assay, and reverse transcription-PCR analysis. The in-vivo angiogenic activity of PlaMSC-exo was evaluated using a murine auricle ischemic injury model. RESULTS: PlaMSC-CM contained both angiogenic and angiostatic factors, which enhanced endothelial tube formation. PlaMSC-exo were incorporated into endothelial cells; these exosomes stimulated both endothelial tube formation and migration, and enhanced angiogenesis-related gene expression. Laser Doppler blood flow analysis showed that PlaMSC-exo infusion also enhanced angiogenesis in an in-vivo murine auricle ischemic injury model. CONCLUSIONS: PlaMSC-exo enhanced angiogenesis in vitro and in vivo, suggesting that exosomes play a role in the proangiogenic activity of PlaMSCs. PlaMSC-exo may be a novel therapeutic approach for treating ischemic diseases. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13287-017-0660-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5627451 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-56274512017-10-12 Exosomes of human placenta-derived mesenchymal stem cells stimulate angiogenesis Komaki, Motohiro Numata, Yuri Morioka, Chikako Honda, Izumi Tooi, Masayuki Yokoyama, Naoki Ayame, Hirohito Iwasaki, Kengo Taki, Atsuko Oshima, Noriko Morita, Ikuo Stem Cell Res Ther Research BACKGROUND: The therapeutic potential of mesenchymal stem cells (MSCs) may be attributed partly to humoral factors such as growth factors, cytokines, and chemokines. Human term placental tissue-derived MSCs (PlaMSCs), or conditioned medium left over from cultures of these cells, have been reported to enhance angiogenesis. Recently, the exosome, which can transport a diverse suite of macromolecules, has gained attention as a novel intercellular communication tool. However, the potential role of the exosome in PlaMSC therapeutic action is not well understood. The purpose of this study was to evaluate PlaMSC-derived exosome angiogenesis promotion in vitro and in vivo. METHODS: MSCs were isolated from human term placental tissue by enzymatic digestion. Conditioned medium was collected after 48-h incubation in serum-free medium (PlaMSC-CM). Angiogenic factors present in PlaMSC-CM were screened by a growth factor array. Exosomes were prepared by ultracentrifugation of PlaMSC-CM, and confirmed by transmission electron microscopy, dynamic light scattering, and western blot analyses. The proangiogenic activity of PlaMSC-derived exosomes (PlaMSC-exo) was assessed using an endothelial tube formation assay, a cell migration assay, and reverse transcription-PCR analysis. The in-vivo angiogenic activity of PlaMSC-exo was evaluated using a murine auricle ischemic injury model. RESULTS: PlaMSC-CM contained both angiogenic and angiostatic factors, which enhanced endothelial tube formation. PlaMSC-exo were incorporated into endothelial cells; these exosomes stimulated both endothelial tube formation and migration, and enhanced angiogenesis-related gene expression. Laser Doppler blood flow analysis showed that PlaMSC-exo infusion also enhanced angiogenesis in an in-vivo murine auricle ischemic injury model. CONCLUSIONS: PlaMSC-exo enhanced angiogenesis in vitro and in vivo, suggesting that exosomes play a role in the proangiogenic activity of PlaMSCs. PlaMSC-exo may be a novel therapeutic approach for treating ischemic diseases. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13287-017-0660-9) contains supplementary material, which is available to authorized users. BioMed Central 2017-10-03 /pmc/articles/PMC5627451/ /pubmed/28974256 http://dx.doi.org/10.1186/s13287-017-0660-9 Text en © The Author(s). 2017 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 Komaki, Motohiro Numata, Yuri Morioka, Chikako Honda, Izumi Tooi, Masayuki Yokoyama, Naoki Ayame, Hirohito Iwasaki, Kengo Taki, Atsuko Oshima, Noriko Morita, Ikuo Exosomes of human placenta-derived mesenchymal stem cells stimulate angiogenesis |
title | Exosomes of human placenta-derived mesenchymal stem cells stimulate angiogenesis |
title_full | Exosomes of human placenta-derived mesenchymal stem cells stimulate angiogenesis |
title_fullStr | Exosomes of human placenta-derived mesenchymal stem cells stimulate angiogenesis |
title_full_unstemmed | Exosomes of human placenta-derived mesenchymal stem cells stimulate angiogenesis |
title_short | Exosomes of human placenta-derived mesenchymal stem cells stimulate angiogenesis |
title_sort | exosomes of human placenta-derived mesenchymal stem cells stimulate angiogenesis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5627451/ https://www.ncbi.nlm.nih.gov/pubmed/28974256 http://dx.doi.org/10.1186/s13287-017-0660-9 |
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