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Rescuing macrophage normal function in spinal cord injury with embryonic stem cell conditioned media

BACKGROUND: Macrophages play an important role in the inflammatory responses involved with spinal cord injury (SCI). We have previously demonstrated that infiltrated bone marrow-derived macrophages (BMDMs) engulf myelin debris, forming myelin-laden macrophages (mye-Mϕ). These mye-Mϕ promote disease...

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Autores principales: Guo, Lei, Rolfe, Alyssa J., Wang, Xi, Tai, Wenjiao, Cheng, Zhijian, Cao, Kai, Chen, Xiaoming, Xu, Yunsheng, Sun, Dongming, Li, Jinhua, He, Xijing, Young, Wise, Fan, Jianqing, Ren, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4858887/
https://www.ncbi.nlm.nih.gov/pubmed/27153974
http://dx.doi.org/10.1186/s13041-016-0233-3
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author Guo, Lei
Rolfe, Alyssa J.
Wang, Xi
Tai, Wenjiao
Cheng, Zhijian
Cao, Kai
Chen, Xiaoming
Xu, Yunsheng
Sun, Dongming
Li, Jinhua
He, Xijing
Young, Wise
Fan, Jianqing
Ren, Yi
author_facet Guo, Lei
Rolfe, Alyssa J.
Wang, Xi
Tai, Wenjiao
Cheng, Zhijian
Cao, Kai
Chen, Xiaoming
Xu, Yunsheng
Sun, Dongming
Li, Jinhua
He, Xijing
Young, Wise
Fan, Jianqing
Ren, Yi
author_sort Guo, Lei
collection PubMed
description BACKGROUND: Macrophages play an important role in the inflammatory responses involved with spinal cord injury (SCI). We have previously demonstrated that infiltrated bone marrow-derived macrophages (BMDMs) engulf myelin debris, forming myelin-laden macrophages (mye-Mϕ). These mye-Mϕ promote disease progression through their pro-inflammatory phenotype, enhanced neurotoxicity, and impaired phagocytic capacity for apoptotic cells. We thus hypothesize that the excessive accumulation of mye-Mϕ is the root of secondary injury, and that targeting mye-Mϕ represents an efficient strategy to improve the local inflammatory microenvironment in injured spinal cords and to further motor neuron function recovery. In this study, we administer murine embryonic stem cell conditioned media (ESC-M) as a cell-free stem cell based therapy to treat a mouse model of SCI. RESULTS: We showed that BMDMs, but not microglial cells, engulf myelin debris generated at the injury site. Phagocytosis of myelin debris leads to the formation of mye-Mϕ in the injured spinal cord, which are surrounded by activated microglia cells. These mye-Mϕ are pro-inflammatory and lose the normal macrophage phagocytic capacity for apoptotic cells. We therefore focus on how to trigger lipid efflux from mye-Mϕ and thus restore their function. Using ESC-M as an immune modulating treatment for inflammatory damage after SCI, we rescued mye-Mϕ function and improved functional locomotor recovery. ESC-M treatment on mye-Mϕ resulted in improved exocytosis of internalized lipids and a normal capacity for apoptotic cell phagocytosis. Furthermore, when ESC-M was administered intraperitoneally after SCI, animals exhibited significant improvements in locomotor recovery. Examination of spinal cords of the ESC-M treated mice revealed similar improvements in macrophage function as well as a shift towards a more anti-inflammatory environment at the lesion and parenchyma. CONCLUSIONS: The embryonic stem cell conditioned media can be used as an effective treatment for SCI to resolve inflammation and improve functional recovery while circumventing the complications involved in whole cell transplantation.
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spelling pubmed-48588872016-05-07 Rescuing macrophage normal function in spinal cord injury with embryonic stem cell conditioned media Guo, Lei Rolfe, Alyssa J. Wang, Xi Tai, Wenjiao Cheng, Zhijian Cao, Kai Chen, Xiaoming Xu, Yunsheng Sun, Dongming Li, Jinhua He, Xijing Young, Wise Fan, Jianqing Ren, Yi Mol Brain Research BACKGROUND: Macrophages play an important role in the inflammatory responses involved with spinal cord injury (SCI). We have previously demonstrated that infiltrated bone marrow-derived macrophages (BMDMs) engulf myelin debris, forming myelin-laden macrophages (mye-Mϕ). These mye-Mϕ promote disease progression through their pro-inflammatory phenotype, enhanced neurotoxicity, and impaired phagocytic capacity for apoptotic cells. We thus hypothesize that the excessive accumulation of mye-Mϕ is the root of secondary injury, and that targeting mye-Mϕ represents an efficient strategy to improve the local inflammatory microenvironment in injured spinal cords and to further motor neuron function recovery. In this study, we administer murine embryonic stem cell conditioned media (ESC-M) as a cell-free stem cell based therapy to treat a mouse model of SCI. RESULTS: We showed that BMDMs, but not microglial cells, engulf myelin debris generated at the injury site. Phagocytosis of myelin debris leads to the formation of mye-Mϕ in the injured spinal cord, which are surrounded by activated microglia cells. These mye-Mϕ are pro-inflammatory and lose the normal macrophage phagocytic capacity for apoptotic cells. We therefore focus on how to trigger lipid efflux from mye-Mϕ and thus restore their function. Using ESC-M as an immune modulating treatment for inflammatory damage after SCI, we rescued mye-Mϕ function and improved functional locomotor recovery. ESC-M treatment on mye-Mϕ resulted in improved exocytosis of internalized lipids and a normal capacity for apoptotic cell phagocytosis. Furthermore, when ESC-M was administered intraperitoneally after SCI, animals exhibited significant improvements in locomotor recovery. Examination of spinal cords of the ESC-M treated mice revealed similar improvements in macrophage function as well as a shift towards a more anti-inflammatory environment at the lesion and parenchyma. CONCLUSIONS: The embryonic stem cell conditioned media can be used as an effective treatment for SCI to resolve inflammation and improve functional recovery while circumventing the complications involved in whole cell transplantation. BioMed Central 2016-05-06 /pmc/articles/PMC4858887/ /pubmed/27153974 http://dx.doi.org/10.1186/s13041-016-0233-3 Text en © Guo et al. 2016 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
Guo, Lei
Rolfe, Alyssa J.
Wang, Xi
Tai, Wenjiao
Cheng, Zhijian
Cao, Kai
Chen, Xiaoming
Xu, Yunsheng
Sun, Dongming
Li, Jinhua
He, Xijing
Young, Wise
Fan, Jianqing
Ren, Yi
Rescuing macrophage normal function in spinal cord injury with embryonic stem cell conditioned media
title Rescuing macrophage normal function in spinal cord injury with embryonic stem cell conditioned media
title_full Rescuing macrophage normal function in spinal cord injury with embryonic stem cell conditioned media
title_fullStr Rescuing macrophage normal function in spinal cord injury with embryonic stem cell conditioned media
title_full_unstemmed Rescuing macrophage normal function in spinal cord injury with embryonic stem cell conditioned media
title_short Rescuing macrophage normal function in spinal cord injury with embryonic stem cell conditioned media
title_sort rescuing macrophage normal function in spinal cord injury with embryonic stem cell conditioned media
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4858887/
https://www.ncbi.nlm.nih.gov/pubmed/27153974
http://dx.doi.org/10.1186/s13041-016-0233-3
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