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Low-level laser facilitates alternatively activated macrophage/microglia polarization and promotes functional recovery after crush spinal cord injury in rats

Macrophages and resident microglia play an import role in the secondary neuroinflammation response following spinal cord injury. Reprogramming of macrophage/microglia polarization is an import strategy for spinal cord injury restoration. Low-level laser therapy (LLLT) is a noninvasive treatment that...

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Autores principales: Song, Ji Wei, Li, Kun, Liang, Zhuo Wen, Dai, Chen, Shen, Xue Feng, Gong, Yu Ze, Wang, Shuang, Hu, Xue Yu, Wang, Zhe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428709/
https://www.ncbi.nlm.nih.gov/pubmed/28377600
http://dx.doi.org/10.1038/s41598-017-00553-6
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author Song, Ji Wei
Li, Kun
Liang, Zhuo Wen
Dai, Chen
Shen, Xue Feng
Gong, Yu Ze
Wang, Shuang
Hu, Xue Yu
Wang, Zhe
author_facet Song, Ji Wei
Li, Kun
Liang, Zhuo Wen
Dai, Chen
Shen, Xue Feng
Gong, Yu Ze
Wang, Shuang
Hu, Xue Yu
Wang, Zhe
author_sort Song, Ji Wei
collection PubMed
description Macrophages and resident microglia play an import role in the secondary neuroinflammation response following spinal cord injury. Reprogramming of macrophage/microglia polarization is an import strategy for spinal cord injury restoration. Low-level laser therapy (LLLT) is a noninvasive treatment that has been widely used in neurotrauma and neurodegenerative diseases. However, the influence of low-level laser on polarization of macrophage/microglia following spinal cord injury remains unknown. The present study applied low-level laser therapy on a crush spinal cord injury rat model. Using immunofluorescence, flow cytometry, RT-qPCR, and western blot assays, we found that low-level laser therapy altered the polarization state to a M2 tendency. A greater number of neurons survived in the pare injury site, which was accompanied by higher BBB scores in the LLLT group. Furthermore, low-level laser therapy elevated expression of interleukin 4 (IL-4) and interleukin 13 (IL-13). Results from this study show that low-level laser therapy has the potential for reducing inflammation, regulating macrophage/microglia polarization, and promoting neuronal survival. These beneficial effects demonstrate that low-level laser therapy may be an effective candidate for clinical treatment of spinal cord injury.
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spelling pubmed-54287092017-05-15 Low-level laser facilitates alternatively activated macrophage/microglia polarization and promotes functional recovery after crush spinal cord injury in rats Song, Ji Wei Li, Kun Liang, Zhuo Wen Dai, Chen Shen, Xue Feng Gong, Yu Ze Wang, Shuang Hu, Xue Yu Wang, Zhe Sci Rep Article Macrophages and resident microglia play an import role in the secondary neuroinflammation response following spinal cord injury. Reprogramming of macrophage/microglia polarization is an import strategy for spinal cord injury restoration. Low-level laser therapy (LLLT) is a noninvasive treatment that has been widely used in neurotrauma and neurodegenerative diseases. However, the influence of low-level laser on polarization of macrophage/microglia following spinal cord injury remains unknown. The present study applied low-level laser therapy on a crush spinal cord injury rat model. Using immunofluorescence, flow cytometry, RT-qPCR, and western blot assays, we found that low-level laser therapy altered the polarization state to a M2 tendency. A greater number of neurons survived in the pare injury site, which was accompanied by higher BBB scores in the LLLT group. Furthermore, low-level laser therapy elevated expression of interleukin 4 (IL-4) and interleukin 13 (IL-13). Results from this study show that low-level laser therapy has the potential for reducing inflammation, regulating macrophage/microglia polarization, and promoting neuronal survival. These beneficial effects demonstrate that low-level laser therapy may be an effective candidate for clinical treatment of spinal cord injury. Nature Publishing Group UK 2017-04-04 /pmc/articles/PMC5428709/ /pubmed/28377600 http://dx.doi.org/10.1038/s41598-017-00553-6 Text en © The Author(s) 2017 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
Song, Ji Wei
Li, Kun
Liang, Zhuo Wen
Dai, Chen
Shen, Xue Feng
Gong, Yu Ze
Wang, Shuang
Hu, Xue Yu
Wang, Zhe
Low-level laser facilitates alternatively activated macrophage/microglia polarization and promotes functional recovery after crush spinal cord injury in rats
title Low-level laser facilitates alternatively activated macrophage/microglia polarization and promotes functional recovery after crush spinal cord injury in rats
title_full Low-level laser facilitates alternatively activated macrophage/microglia polarization and promotes functional recovery after crush spinal cord injury in rats
title_fullStr Low-level laser facilitates alternatively activated macrophage/microglia polarization and promotes functional recovery after crush spinal cord injury in rats
title_full_unstemmed Low-level laser facilitates alternatively activated macrophage/microglia polarization and promotes functional recovery after crush spinal cord injury in rats
title_short Low-level laser facilitates alternatively activated macrophage/microglia polarization and promotes functional recovery after crush spinal cord injury in rats
title_sort low-level laser facilitates alternatively activated macrophage/microglia polarization and promotes functional recovery after crush spinal cord injury in rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428709/
https://www.ncbi.nlm.nih.gov/pubmed/28377600
http://dx.doi.org/10.1038/s41598-017-00553-6
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