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Increased plasma VEGF levels following ischemic preconditioning are associated with downregulation of miRNA-762 and miR-3072-5p
Ischemic preconditioning (IPC) has protective effects against ischemia-perfusion injury of organs. In the present study, we investigated the associated mechanisms after performing remote IPC (rIPC) of lower limbs by clamping abdominal aorta in mice. Subsequent experiments showed decreased damage and...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5131337/ https://www.ncbi.nlm.nih.gov/pubmed/27905554 http://dx.doi.org/10.1038/srep36758 |
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author | Ueno, Koji Samura, Makoto Nakamura, Tamami Tanaka, Yuya Takeuchi, Yuriko Kawamura, Daichi Takahashi, Masaya Hosoyama, Tohru Morikage, Noriyasu Hamano, Kimikazu |
author_facet | Ueno, Koji Samura, Makoto Nakamura, Tamami Tanaka, Yuya Takeuchi, Yuriko Kawamura, Daichi Takahashi, Masaya Hosoyama, Tohru Morikage, Noriyasu Hamano, Kimikazu |
author_sort | Ueno, Koji |
collection | PubMed |
description | Ischemic preconditioning (IPC) has protective effects against ischemia-perfusion injury of organs. In the present study, we investigated the associated mechanisms after performing remote IPC (rIPC) of lower limbs by clamping abdominal aorta in mice. Subsequent experiments showed decreased damage and paralysis of lower limbs following spinal cord injury (SCI). Concomitantly, plasma vascular endothelial growth factor (VEGF) levels were increased 24 h after rIPC compared with those in sham-operated animals. In subsequent microRNA analyses, thirteen microRNAs were downregulated in exosomes 24 h after rIPC. Further studies of femoral CD34-positive bone marrow (BM) cells confirmed downregulation of these seven microRNAs 24 h after rIPC compared with those in sham-operated controls. Subsequent algorithm-based database searches suggested that two of the seven microRNAs bind to the 3′ UTR of VEGF mRNA, and following transfection into CD34-positive BM cells, anti-miR-762, and anti-miR-3072-5p inhibitors led to increased VEGF concentrations. The present data suggest that rIPC transiently increases plasma VEGF levels by downregulating miR-762 and miR-3072-5p in CD34-positive BM cells, leading to protection against organ ischemia. |
format | Online Article Text |
id | pubmed-5131337 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-51313372016-12-15 Increased plasma VEGF levels following ischemic preconditioning are associated with downregulation of miRNA-762 and miR-3072-5p Ueno, Koji Samura, Makoto Nakamura, Tamami Tanaka, Yuya Takeuchi, Yuriko Kawamura, Daichi Takahashi, Masaya Hosoyama, Tohru Morikage, Noriyasu Hamano, Kimikazu Sci Rep Article Ischemic preconditioning (IPC) has protective effects against ischemia-perfusion injury of organs. In the present study, we investigated the associated mechanisms after performing remote IPC (rIPC) of lower limbs by clamping abdominal aorta in mice. Subsequent experiments showed decreased damage and paralysis of lower limbs following spinal cord injury (SCI). Concomitantly, plasma vascular endothelial growth factor (VEGF) levels were increased 24 h after rIPC compared with those in sham-operated animals. In subsequent microRNA analyses, thirteen microRNAs were downregulated in exosomes 24 h after rIPC. Further studies of femoral CD34-positive bone marrow (BM) cells confirmed downregulation of these seven microRNAs 24 h after rIPC compared with those in sham-operated controls. Subsequent algorithm-based database searches suggested that two of the seven microRNAs bind to the 3′ UTR of VEGF mRNA, and following transfection into CD34-positive BM cells, anti-miR-762, and anti-miR-3072-5p inhibitors led to increased VEGF concentrations. The present data suggest that rIPC transiently increases plasma VEGF levels by downregulating miR-762 and miR-3072-5p in CD34-positive BM cells, leading to protection against organ ischemia. Nature Publishing Group 2016-12-01 /pmc/articles/PMC5131337/ /pubmed/27905554 http://dx.doi.org/10.1038/srep36758 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Ueno, Koji Samura, Makoto Nakamura, Tamami Tanaka, Yuya Takeuchi, Yuriko Kawamura, Daichi Takahashi, Masaya Hosoyama, Tohru Morikage, Noriyasu Hamano, Kimikazu Increased plasma VEGF levels following ischemic preconditioning are associated with downregulation of miRNA-762 and miR-3072-5p |
title | Increased plasma VEGF levels following ischemic preconditioning are associated with downregulation of miRNA-762 and miR-3072-5p |
title_full | Increased plasma VEGF levels following ischemic preconditioning are associated with downregulation of miRNA-762 and miR-3072-5p |
title_fullStr | Increased plasma VEGF levels following ischemic preconditioning are associated with downregulation of miRNA-762 and miR-3072-5p |
title_full_unstemmed | Increased plasma VEGF levels following ischemic preconditioning are associated with downregulation of miRNA-762 and miR-3072-5p |
title_short | Increased plasma VEGF levels following ischemic preconditioning are associated with downregulation of miRNA-762 and miR-3072-5p |
title_sort | increased plasma vegf levels following ischemic preconditioning are associated with downregulation of mirna-762 and mir-3072-5p |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5131337/ https://www.ncbi.nlm.nih.gov/pubmed/27905554 http://dx.doi.org/10.1038/srep36758 |
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