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Genetically modified mesenchymal stem cells promote spinal fusion through polarized macrophages

Spinal fusion is an effective treatment for low back pain and typically applied with prosthetic fixation devices. Spinal fusion can be improved by transplantation of mesenchymal stem cells (MSCs) into the paraspinal muscle. However, in contrast to the direct contribution of MSCs to spinal fusion, th...

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Autores principales: Yu, Luchao, Shi, Qiang, Zhang, Baokun, Xu, Jianguang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8860744/
https://www.ncbi.nlm.nih.gov/pubmed/34764437
http://dx.doi.org/10.1038/s41374-021-00693-4
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author Yu, Luchao
Shi, Qiang
Zhang, Baokun
Xu, Jianguang
author_facet Yu, Luchao
Shi, Qiang
Zhang, Baokun
Xu, Jianguang
author_sort Yu, Luchao
collection PubMed
description Spinal fusion is an effective treatment for low back pain and typically applied with prosthetic fixation devices. Spinal fusion can be improved by transplantation of mesenchymal stem cells (MSCs) into the paraspinal muscle. However, in contrast to the direct contribution of MSCs to spinal fusion, the indirect effects of MSCs on spinal infusion have not been studied and were thus addressed here. The correlation between the outcome of spinal fusion and the local macrophage number, polarization and the levels of placental growth factor (PlGF) in patients was analyzed. MSCs were genetically modified to overexpress PlGF, and its effects on macrophage proliferation and polarization were analyzed in vitro in a transwell co-culture system, as well as in vivo in a mouse model for spinal fusion, for which the cells were bilaterally injected into paravertebral muscles of the mouse lumbar spine. The effects on spinal fusion were assessed by microcomputed tomography and a custom four-point bending apparatus for structural bending stiffness. Local macrophages were analyzed by flow cytometry. We found that posterior spinal fusion could be improved by PlGF-expressing MSCs, compared to the control MSCs, evident by significant improvement of bone bridging of the targeted vertebrae. Mechanistically, PlGF-expressing MSCs appeared to attract macrophages and induce their M2 polarization, which in turn promotes the bone formation. Together, our data suggest that PlGF-expressing MSCs may improve spinal fusion through macrophage recruitment and polarization.
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spelling pubmed-88607442022-03-15 Genetically modified mesenchymal stem cells promote spinal fusion through polarized macrophages Yu, Luchao Shi, Qiang Zhang, Baokun Xu, Jianguang Lab Invest Article Spinal fusion is an effective treatment for low back pain and typically applied with prosthetic fixation devices. Spinal fusion can be improved by transplantation of mesenchymal stem cells (MSCs) into the paraspinal muscle. However, in contrast to the direct contribution of MSCs to spinal fusion, the indirect effects of MSCs on spinal infusion have not been studied and were thus addressed here. The correlation between the outcome of spinal fusion and the local macrophage number, polarization and the levels of placental growth factor (PlGF) in patients was analyzed. MSCs were genetically modified to overexpress PlGF, and its effects on macrophage proliferation and polarization were analyzed in vitro in a transwell co-culture system, as well as in vivo in a mouse model for spinal fusion, for which the cells were bilaterally injected into paravertebral muscles of the mouse lumbar spine. The effects on spinal fusion were assessed by microcomputed tomography and a custom four-point bending apparatus for structural bending stiffness. Local macrophages were analyzed by flow cytometry. We found that posterior spinal fusion could be improved by PlGF-expressing MSCs, compared to the control MSCs, evident by significant improvement of bone bridging of the targeted vertebrae. Mechanistically, PlGF-expressing MSCs appeared to attract macrophages and induce their M2 polarization, which in turn promotes the bone formation. Together, our data suggest that PlGF-expressing MSCs may improve spinal fusion through macrophage recruitment and polarization. Nature Publishing Group US 2021-11-11 2022 /pmc/articles/PMC8860744/ /pubmed/34764437 http://dx.doi.org/10.1038/s41374-021-00693-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Yu, Luchao
Shi, Qiang
Zhang, Baokun
Xu, Jianguang
Genetically modified mesenchymal stem cells promote spinal fusion through polarized macrophages
title Genetically modified mesenchymal stem cells promote spinal fusion through polarized macrophages
title_full Genetically modified mesenchymal stem cells promote spinal fusion through polarized macrophages
title_fullStr Genetically modified mesenchymal stem cells promote spinal fusion through polarized macrophages
title_full_unstemmed Genetically modified mesenchymal stem cells promote spinal fusion through polarized macrophages
title_short Genetically modified mesenchymal stem cells promote spinal fusion through polarized macrophages
title_sort genetically modified mesenchymal stem cells promote spinal fusion through polarized macrophages
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8860744/
https://www.ncbi.nlm.nih.gov/pubmed/34764437
http://dx.doi.org/10.1038/s41374-021-00693-4
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