Cargando…
Magnetic Stimulation Drives Macrophage Polarization in Cell to–Cell Communication with IL-1β Primed Tendon Cells
Inflammation is part of the natural healing response, but it has been simultaneously associated with tendon disorders, as persistent inflammatory events contribute to physiological changes that compromise tendon functions. The cellular interactions within a niche are extremely important for healing....
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7432806/ https://www.ncbi.nlm.nih.gov/pubmed/32751697 http://dx.doi.org/10.3390/ijms21155441 |
_version_ | 1783571879256129536 |
---|---|
author | Vinhas, Adriana Almeida, Ana F. Gonçalves, Ana I. Rodrigues, Márcia T. Gomes, Manuela E. |
author_facet | Vinhas, Adriana Almeida, Ana F. Gonçalves, Ana I. Rodrigues, Márcia T. Gomes, Manuela E. |
author_sort | Vinhas, Adriana |
collection | PubMed |
description | Inflammation is part of the natural healing response, but it has been simultaneously associated with tendon disorders, as persistent inflammatory events contribute to physiological changes that compromise tendon functions. The cellular interactions within a niche are extremely important for healing. While human tendon cells (hTDCs) are responsible for the maintenance of tendon matrix and turnover, macrophages regulate healing switching their functional phenotype to environmental stimuli. Thus, insights on the hTDCs and macrophages interactions can provide fundamental contributions on tendon repair mechanisms and on the inflammatory inputs in tendon disorders. We explored the crosstalk between macrophages and hTDCs using co-culture approaches in which hTDCs were previously stimulated with IL-1β. The potential modulatory effect of the pulsed electromagnetic field (PEMF) in macrophage-hTDCs communication was also investigated using the magnetic parameters identified in a previous work. The PEMF influences a macrophage pro-regenerative phenotype and favors the synthesis of anti-inflammatory mediators. These outcomes observed in cell contact co-cultures may be mediated by FAK signaling. The impact of the PEMF overcomes the effect of IL-1β-treated-hTDCs, supporting PEMF immunomodulatory actions on macrophages. This work highlights the relevance of intercellular communication in tendon healing and the beneficial role of the PEMF in guiding inflammatory responses toward regenerative strategies. |
format | Online Article Text |
id | pubmed-7432806 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-74328062020-08-27 Magnetic Stimulation Drives Macrophage Polarization in Cell to–Cell Communication with IL-1β Primed Tendon Cells Vinhas, Adriana Almeida, Ana F. Gonçalves, Ana I. Rodrigues, Márcia T. Gomes, Manuela E. Int J Mol Sci Article Inflammation is part of the natural healing response, but it has been simultaneously associated with tendon disorders, as persistent inflammatory events contribute to physiological changes that compromise tendon functions. The cellular interactions within a niche are extremely important for healing. While human tendon cells (hTDCs) are responsible for the maintenance of tendon matrix and turnover, macrophages regulate healing switching their functional phenotype to environmental stimuli. Thus, insights on the hTDCs and macrophages interactions can provide fundamental contributions on tendon repair mechanisms and on the inflammatory inputs in tendon disorders. We explored the crosstalk between macrophages and hTDCs using co-culture approaches in which hTDCs were previously stimulated with IL-1β. The potential modulatory effect of the pulsed electromagnetic field (PEMF) in macrophage-hTDCs communication was also investigated using the magnetic parameters identified in a previous work. The PEMF influences a macrophage pro-regenerative phenotype and favors the synthesis of anti-inflammatory mediators. These outcomes observed in cell contact co-cultures may be mediated by FAK signaling. The impact of the PEMF overcomes the effect of IL-1β-treated-hTDCs, supporting PEMF immunomodulatory actions on macrophages. This work highlights the relevance of intercellular communication in tendon healing and the beneficial role of the PEMF in guiding inflammatory responses toward regenerative strategies. MDPI 2020-07-30 /pmc/articles/PMC7432806/ /pubmed/32751697 http://dx.doi.org/10.3390/ijms21155441 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Vinhas, Adriana Almeida, Ana F. Gonçalves, Ana I. Rodrigues, Márcia T. Gomes, Manuela E. Magnetic Stimulation Drives Macrophage Polarization in Cell to–Cell Communication with IL-1β Primed Tendon Cells |
title | Magnetic Stimulation Drives Macrophage Polarization in Cell to–Cell Communication with IL-1β Primed Tendon Cells |
title_full | Magnetic Stimulation Drives Macrophage Polarization in Cell to–Cell Communication with IL-1β Primed Tendon Cells |
title_fullStr | Magnetic Stimulation Drives Macrophage Polarization in Cell to–Cell Communication with IL-1β Primed Tendon Cells |
title_full_unstemmed | Magnetic Stimulation Drives Macrophage Polarization in Cell to–Cell Communication with IL-1β Primed Tendon Cells |
title_short | Magnetic Stimulation Drives Macrophage Polarization in Cell to–Cell Communication with IL-1β Primed Tendon Cells |
title_sort | magnetic stimulation drives macrophage polarization in cell to–cell communication with il-1β primed tendon cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7432806/ https://www.ncbi.nlm.nih.gov/pubmed/32751697 http://dx.doi.org/10.3390/ijms21155441 |
work_keys_str_mv | AT vinhasadriana magneticstimulationdrivesmacrophagepolarizationincelltocellcommunicationwithil1bprimedtendoncells AT almeidaanaf magneticstimulationdrivesmacrophagepolarizationincelltocellcommunicationwithil1bprimedtendoncells AT goncalvesanai magneticstimulationdrivesmacrophagepolarizationincelltocellcommunicationwithil1bprimedtendoncells AT rodriguesmarciat magneticstimulationdrivesmacrophagepolarizationincelltocellcommunicationwithil1bprimedtendoncells AT gomesmanuelae magneticstimulationdrivesmacrophagepolarizationincelltocellcommunicationwithil1bprimedtendoncells |