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Macrophages Characterization in an Injured Bone Tissue
Biomaterial use is a promising approach to facilitate wound healing of the bone tissue. Biomaterials induce the formation of membrane capsules and the recruitment of different types of macrophages. Macrophages are immune cells that produce diverse combinations of cytokines playing an important role...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9219779/ https://www.ncbi.nlm.nih.gov/pubmed/35740407 http://dx.doi.org/10.3390/biomedicines10061385 |
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author | Nikovics, Krisztina Durand, Marjorie Castellarin, Cédric Burger, Julien Sicherre, Emma Collombet, Jean-Marc Oger, Myriam Holy, Xavier Favier, Anne-Laure |
author_facet | Nikovics, Krisztina Durand, Marjorie Castellarin, Cédric Burger, Julien Sicherre, Emma Collombet, Jean-Marc Oger, Myriam Holy, Xavier Favier, Anne-Laure |
author_sort | Nikovics, Krisztina |
collection | PubMed |
description | Biomaterial use is a promising approach to facilitate wound healing of the bone tissue. Biomaterials induce the formation of membrane capsules and the recruitment of different types of macrophages. Macrophages are immune cells that produce diverse combinations of cytokines playing an important role in bone healing and regeneration, but the exact mechanism remains to be studied. Our work aimed to identify in vivo macrophages in the Masquelet induced membrane in a rat model. Most of the macrophages in the damaged area were M2-like, with smaller numbers of M1-like macrophages. In addition, high expression of IL-1β and IL-6 cytokines were detected in the membrane region by RT-qPCR. Using an innovative combination of two hybridization techniques (in situ hybridization and in situ hybridization chain reaction (in situ HCR)), M2b-like macrophages were identified for the first time in cryosections of non-decalcified bone. Our work has also demonstrated that microspectroscopical analysis is essential for macrophage characterization, as it allows the discrimination of fluorescence and autofluorescence. Finally, this work has revealed the limitations of immunolabelling and the potential of in situ HCR to provide valuable information for in vivo characterization of macrophages. |
format | Online Article Text |
id | pubmed-9219779 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-92197792022-06-24 Macrophages Characterization in an Injured Bone Tissue Nikovics, Krisztina Durand, Marjorie Castellarin, Cédric Burger, Julien Sicherre, Emma Collombet, Jean-Marc Oger, Myriam Holy, Xavier Favier, Anne-Laure Biomedicines Technical Note Biomaterial use is a promising approach to facilitate wound healing of the bone tissue. Biomaterials induce the formation of membrane capsules and the recruitment of different types of macrophages. Macrophages are immune cells that produce diverse combinations of cytokines playing an important role in bone healing and regeneration, but the exact mechanism remains to be studied. Our work aimed to identify in vivo macrophages in the Masquelet induced membrane in a rat model. Most of the macrophages in the damaged area were M2-like, with smaller numbers of M1-like macrophages. In addition, high expression of IL-1β and IL-6 cytokines were detected in the membrane region by RT-qPCR. Using an innovative combination of two hybridization techniques (in situ hybridization and in situ hybridization chain reaction (in situ HCR)), M2b-like macrophages were identified for the first time in cryosections of non-decalcified bone. Our work has also demonstrated that microspectroscopical analysis is essential for macrophage characterization, as it allows the discrimination of fluorescence and autofluorescence. Finally, this work has revealed the limitations of immunolabelling and the potential of in situ HCR to provide valuable information for in vivo characterization of macrophages. MDPI 2022-06-11 /pmc/articles/PMC9219779/ /pubmed/35740407 http://dx.doi.org/10.3390/biomedicines10061385 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Technical Note Nikovics, Krisztina Durand, Marjorie Castellarin, Cédric Burger, Julien Sicherre, Emma Collombet, Jean-Marc Oger, Myriam Holy, Xavier Favier, Anne-Laure Macrophages Characterization in an Injured Bone Tissue |
title | Macrophages Characterization in an Injured Bone Tissue |
title_full | Macrophages Characterization in an Injured Bone Tissue |
title_fullStr | Macrophages Characterization in an Injured Bone Tissue |
title_full_unstemmed | Macrophages Characterization in an Injured Bone Tissue |
title_short | Macrophages Characterization in an Injured Bone Tissue |
title_sort | macrophages characterization in an injured bone tissue |
topic | Technical Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9219779/ https://www.ncbi.nlm.nih.gov/pubmed/35740407 http://dx.doi.org/10.3390/biomedicines10061385 |
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