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Precise immunomodulation of the M1 to M2 macrophage transition enhances mesenchymal stem cell osteogenesis and differs by sex

OBJECTIVES: Up to 10% of fractures result in undesirable outcomes, for which female sex is a risk factor. Cellular sex differences have been implicated in these different healing processes. Better understanding of the mechanisms underlying bone healing and sex differences in this process is key to i...

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Autores principales: Nathan, Karthik, Lu, Laura Y., Lin, Tzuhua, Pajarinen, Jukka, Jämsen, Eemeli, Huang, Jhih-Fong, Romero-Lopez, Monica, Maruyama, Masahiro, Kohno, Yusuke, Yao, Zhenyu, Goodman, Stuart B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6825050/
https://www.ncbi.nlm.nih.gov/pubmed/31728188
http://dx.doi.org/10.1302/2046-3758.810.BJR-2018-0231.R2
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author Nathan, Karthik
Lu, Laura Y.
Lin, Tzuhua
Pajarinen, Jukka
Jämsen, Eemeli
Huang, Jhih-Fong
Romero-Lopez, Monica
Maruyama, Masahiro
Kohno, Yusuke
Yao, Zhenyu
Goodman, Stuart B.
author_facet Nathan, Karthik
Lu, Laura Y.
Lin, Tzuhua
Pajarinen, Jukka
Jämsen, Eemeli
Huang, Jhih-Fong
Romero-Lopez, Monica
Maruyama, Masahiro
Kohno, Yusuke
Yao, Zhenyu
Goodman, Stuart B.
author_sort Nathan, Karthik
collection PubMed
description OBJECTIVES: Up to 10% of fractures result in undesirable outcomes, for which female sex is a risk factor. Cellular sex differences have been implicated in these different healing processes. Better understanding of the mechanisms underlying bone healing and sex differences in this process is key to improved clinical outcomes. This study utilized a macrophage–mesenchymal stem cell (MSC) coculture system to determine: 1) the precise timing of proinflammatory (M1) to anti-inflammatory (M2) macrophage transition for optimal bone formation; and 2) how such immunomodulation was affected by male versus female cocultures. METHODS: A primary murine macrophage-MSC coculture system was used to demonstrate the optimal transition time from M1 to M2 (polarized from M1 with interleukin (IL)-4) macrophages to maximize matrix mineralization in male and female MSCs. Outcome variables included Alizarin Red staining, alkaline phosphatase (ALP) activity, and osteocalcin protein secretion. RESULTS: We found that 96 hours of M1 phenotype in male cocultures allowed for maximum matrix mineralization versus 72 hours in female cocultures. ALP activity and osteocalcin secretion were also enhanced with the addition of IL-4 later in male versus female groups. The sex of the cells had a statistically significant effect on the optimal IL-4 addition time to maximize osteogenesis. CONCLUSION: These results suggest that: 1) a 72- to 96-hour proinflammatory environment is critical for optimal matrix mineralization; and 2) there are immunological differences in this coculture environment due to sex. Optimizing immunomodulation during fracture healing may enhance and expedite the bone regeneration response. These findings provide insight into precise immunomodulation for enhanced bone healing that is sex-specific. Cite this article: K. Nathan, L. Y. Lu, T. Lin, J. Pajarinen, E. Jämsen, J-F. Huang, M. Romero-Lopez, M. Maruyama, Y. Kohno, Z. Yao, S. B. Goodman. Precise immunomodulation of the M1 to M2 macrophage transition enhances mesenchymal stem cell osteogenesis and differs by sex. Bone Joint Res 2019;8:481–488. DOI: 10.1302/2046-3758.810.BJR-2018-0231.R2.
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spelling pubmed-68250502019-11-14 Precise immunomodulation of the M1 to M2 macrophage transition enhances mesenchymal stem cell osteogenesis and differs by sex Nathan, Karthik Lu, Laura Y. Lin, Tzuhua Pajarinen, Jukka Jämsen, Eemeli Huang, Jhih-Fong Romero-Lopez, Monica Maruyama, Masahiro Kohno, Yusuke Yao, Zhenyu Goodman, Stuart B. Bone Joint Res Bone Biology OBJECTIVES: Up to 10% of fractures result in undesirable outcomes, for which female sex is a risk factor. Cellular sex differences have been implicated in these different healing processes. Better understanding of the mechanisms underlying bone healing and sex differences in this process is key to improved clinical outcomes. This study utilized a macrophage–mesenchymal stem cell (MSC) coculture system to determine: 1) the precise timing of proinflammatory (M1) to anti-inflammatory (M2) macrophage transition for optimal bone formation; and 2) how such immunomodulation was affected by male versus female cocultures. METHODS: A primary murine macrophage-MSC coculture system was used to demonstrate the optimal transition time from M1 to M2 (polarized from M1 with interleukin (IL)-4) macrophages to maximize matrix mineralization in male and female MSCs. Outcome variables included Alizarin Red staining, alkaline phosphatase (ALP) activity, and osteocalcin protein secretion. RESULTS: We found that 96 hours of M1 phenotype in male cocultures allowed for maximum matrix mineralization versus 72 hours in female cocultures. ALP activity and osteocalcin secretion were also enhanced with the addition of IL-4 later in male versus female groups. The sex of the cells had a statistically significant effect on the optimal IL-4 addition time to maximize osteogenesis. CONCLUSION: These results suggest that: 1) a 72- to 96-hour proinflammatory environment is critical for optimal matrix mineralization; and 2) there are immunological differences in this coculture environment due to sex. Optimizing immunomodulation during fracture healing may enhance and expedite the bone regeneration response. These findings provide insight into precise immunomodulation for enhanced bone healing that is sex-specific. Cite this article: K. Nathan, L. Y. Lu, T. Lin, J. Pajarinen, E. Jämsen, J-F. Huang, M. Romero-Lopez, M. Maruyama, Y. Kohno, Z. Yao, S. B. Goodman. Precise immunomodulation of the M1 to M2 macrophage transition enhances mesenchymal stem cell osteogenesis and differs by sex. Bone Joint Res 2019;8:481–488. DOI: 10.1302/2046-3758.810.BJR-2018-0231.R2. 2019-11-02 /pmc/articles/PMC6825050/ /pubmed/31728188 http://dx.doi.org/10.1302/2046-3758.810.BJR-2018-0231.R2 Text en © 2019 Author(s) et al Open Access This is an open-access article distributed under the terms of the Creative Commons Attributions licence (CC-BY-NC), which permits unrestricted use, distribution, and reproduction in any medium, but not for commercial gain, provided the original author and source are credited.
spellingShingle Bone Biology
Nathan, Karthik
Lu, Laura Y.
Lin, Tzuhua
Pajarinen, Jukka
Jämsen, Eemeli
Huang, Jhih-Fong
Romero-Lopez, Monica
Maruyama, Masahiro
Kohno, Yusuke
Yao, Zhenyu
Goodman, Stuart B.
Precise immunomodulation of the M1 to M2 macrophage transition enhances mesenchymal stem cell osteogenesis and differs by sex
title Precise immunomodulation of the M1 to M2 macrophage transition enhances mesenchymal stem cell osteogenesis and differs by sex
title_full Precise immunomodulation of the M1 to M2 macrophage transition enhances mesenchymal stem cell osteogenesis and differs by sex
title_fullStr Precise immunomodulation of the M1 to M2 macrophage transition enhances mesenchymal stem cell osteogenesis and differs by sex
title_full_unstemmed Precise immunomodulation of the M1 to M2 macrophage transition enhances mesenchymal stem cell osteogenesis and differs by sex
title_short Precise immunomodulation of the M1 to M2 macrophage transition enhances mesenchymal stem cell osteogenesis and differs by sex
title_sort precise immunomodulation of the m1 to m2 macrophage transition enhances mesenchymal stem cell osteogenesis and differs by sex
topic Bone Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6825050/
https://www.ncbi.nlm.nih.gov/pubmed/31728188
http://dx.doi.org/10.1302/2046-3758.810.BJR-2018-0231.R2
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