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Intravenous injection of neural progenitor cells facilitates angiogenesis after cerebral ischemia
Earlier we demonstrated that the injection of neural progenitor cells (NPCs) has therapeutic potential for the improvement of learning dysfunction after cerebral ischemia. However, it remained to be clarified how transplantation of NPCs can improve ischemia-induced dysfunction. In this study, we exa...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3607146/ https://www.ncbi.nlm.nih.gov/pubmed/23532762 http://dx.doi.org/10.1002/brb3.113 |
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author | Moriyama, Yoshiyuki Takagi, Norio Hashimura, Kanae Itokawa, Chisa Tanonaka, Kouichi |
author_facet | Moriyama, Yoshiyuki Takagi, Norio Hashimura, Kanae Itokawa, Chisa Tanonaka, Kouichi |
author_sort | Moriyama, Yoshiyuki |
collection | PubMed |
description | Earlier we demonstrated that the injection of neural progenitor cells (NPCs) has therapeutic potential for the improvement of learning dysfunction after cerebral ischemia. However, it remained to be clarified how transplantation of NPCs can improve ischemia-induced dysfunction. In this study, we examined whether intravenous injection of NPCs after cerebral ischemia could enhance angiogenesis by affecting the expression of angiogenic factors. The injection of NPCs on day 7 after cerebral ischemia enhanced angiogenesis on day 28. Vascular endothelial growth factor (VEGF) and its receptor VEGFR2 were increased in expression by the NPC injection. The level of angiopoietin-1 (Ang-1), an angiogenic factor, but not that of Ang-2, which acts as an antagonist for the Ang-1 receptor, was also increased on day 28. In addition, the expression of Ang-1 receptor Tie2 was enhanced in brain capillaries. Furthermore, the amounts of tight junctional proteins, which are in the blood–brain barrier and whose expression occurs downstream of Ang-1/Tie2 signaling, were increased by the NPC injection. These results suggest that the NPC injection promoted angiogenesis through Ang-1/Tie2 and/or VEGF/VEGFR2 signaling in brain capillaries after cerebral ischemia. Such signaling might have the potential for causing vascular stabilization and maturation for a long period after cerebral ischemia. |
format | Online Article Text |
id | pubmed-3607146 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-36071462013-03-25 Intravenous injection of neural progenitor cells facilitates angiogenesis after cerebral ischemia Moriyama, Yoshiyuki Takagi, Norio Hashimura, Kanae Itokawa, Chisa Tanonaka, Kouichi Brain Behav Original Research Earlier we demonstrated that the injection of neural progenitor cells (NPCs) has therapeutic potential for the improvement of learning dysfunction after cerebral ischemia. However, it remained to be clarified how transplantation of NPCs can improve ischemia-induced dysfunction. In this study, we examined whether intravenous injection of NPCs after cerebral ischemia could enhance angiogenesis by affecting the expression of angiogenic factors. The injection of NPCs on day 7 after cerebral ischemia enhanced angiogenesis on day 28. Vascular endothelial growth factor (VEGF) and its receptor VEGFR2 were increased in expression by the NPC injection. The level of angiopoietin-1 (Ang-1), an angiogenic factor, but not that of Ang-2, which acts as an antagonist for the Ang-1 receptor, was also increased on day 28. In addition, the expression of Ang-1 receptor Tie2 was enhanced in brain capillaries. Furthermore, the amounts of tight junctional proteins, which are in the blood–brain barrier and whose expression occurs downstream of Ang-1/Tie2 signaling, were increased by the NPC injection. These results suggest that the NPC injection promoted angiogenesis through Ang-1/Tie2 and/or VEGF/VEGFR2 signaling in brain capillaries after cerebral ischemia. Such signaling might have the potential for causing vascular stabilization and maturation for a long period after cerebral ischemia. Blackwell Publishing Ltd 2013-03 2012-12-28 /pmc/articles/PMC3607146/ /pubmed/23532762 http://dx.doi.org/10.1002/brb3.113 Text en © 2013 Published by Wiley Periodicals, Inc. http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation. |
spellingShingle | Original Research Moriyama, Yoshiyuki Takagi, Norio Hashimura, Kanae Itokawa, Chisa Tanonaka, Kouichi Intravenous injection of neural progenitor cells facilitates angiogenesis after cerebral ischemia |
title | Intravenous injection of neural progenitor cells facilitates angiogenesis after cerebral ischemia |
title_full | Intravenous injection of neural progenitor cells facilitates angiogenesis after cerebral ischemia |
title_fullStr | Intravenous injection of neural progenitor cells facilitates angiogenesis after cerebral ischemia |
title_full_unstemmed | Intravenous injection of neural progenitor cells facilitates angiogenesis after cerebral ischemia |
title_short | Intravenous injection of neural progenitor cells facilitates angiogenesis after cerebral ischemia |
title_sort | intravenous injection of neural progenitor cells facilitates angiogenesis after cerebral ischemia |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3607146/ https://www.ncbi.nlm.nih.gov/pubmed/23532762 http://dx.doi.org/10.1002/brb3.113 |
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