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The impact of wavelengths of LED light-therapy on endothelial cells

Low level light therapy receives increasing interest in the fields of tissue regeneration and wound healing. Several in vivo studies demonstrated the positive effects of LLLT on angiogenesis. This study aimed to investigate the underlying properties in vitro by comparing the effects of light therapy...

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Autores principales: Rohringer, Sabrina, Holnthoner, Wolfgang, Chaudary, Sidrah, Slezak, Paul, Priglinger, Eleni, Strassl, Martin, Pill, Karoline, Mühleder, Severin, Redl, Heinz, Dungel, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5587748/
https://www.ncbi.nlm.nih.gov/pubmed/28878330
http://dx.doi.org/10.1038/s41598-017-11061-y
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author Rohringer, Sabrina
Holnthoner, Wolfgang
Chaudary, Sidrah
Slezak, Paul
Priglinger, Eleni
Strassl, Martin
Pill, Karoline
Mühleder, Severin
Redl, Heinz
Dungel, Peter
author_facet Rohringer, Sabrina
Holnthoner, Wolfgang
Chaudary, Sidrah
Slezak, Paul
Priglinger, Eleni
Strassl, Martin
Pill, Karoline
Mühleder, Severin
Redl, Heinz
Dungel, Peter
author_sort Rohringer, Sabrina
collection PubMed
description Low level light therapy receives increasing interest in the fields of tissue regeneration and wound healing. Several in vivo studies demonstrated the positive effects of LLLT on angiogenesis. This study aimed to investigate the underlying properties in vitro by comparing the effects of light therapy by light emitting diodes of different wavelengths on endothelial cells in vitro. Human umbilical vein endothelial cells were treated with either 475 nm, 516 nm or 635 nm light. Control cells were not illuminated. 2D proliferation was quantified by manual counting. HUVEC migration was analyzed by performing a 2D wound scratch assay and a 3D bead assay. The influence of LLLT on early vasculogenic events was determined in a 3D fibrin co-culture model with adipose-derived stem cells. Stimulation with both red and green pulsed LED light significantly increased HUVEC proliferation and 3D migration. Moreover, HUVEC showed increased 2D migration potential with green light stimulation. The treatment with blue light was ineffective. Several parameters showed that green light was even more potent to stimulate proliferation and migration of endothelial cells than clinically well-established red light therapy. Further studies have to focus on intracellular mechanisms induced by different wavelengths in order to optimize this promising therapy in tissue regeneration.
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spelling pubmed-55877482017-09-13 The impact of wavelengths of LED light-therapy on endothelial cells Rohringer, Sabrina Holnthoner, Wolfgang Chaudary, Sidrah Slezak, Paul Priglinger, Eleni Strassl, Martin Pill, Karoline Mühleder, Severin Redl, Heinz Dungel, Peter Sci Rep Article Low level light therapy receives increasing interest in the fields of tissue regeneration and wound healing. Several in vivo studies demonstrated the positive effects of LLLT on angiogenesis. This study aimed to investigate the underlying properties in vitro by comparing the effects of light therapy by light emitting diodes of different wavelengths on endothelial cells in vitro. Human umbilical vein endothelial cells were treated with either 475 nm, 516 nm or 635 nm light. Control cells were not illuminated. 2D proliferation was quantified by manual counting. HUVEC migration was analyzed by performing a 2D wound scratch assay and a 3D bead assay. The influence of LLLT on early vasculogenic events was determined in a 3D fibrin co-culture model with adipose-derived stem cells. Stimulation with both red and green pulsed LED light significantly increased HUVEC proliferation and 3D migration. Moreover, HUVEC showed increased 2D migration potential with green light stimulation. The treatment with blue light was ineffective. Several parameters showed that green light was even more potent to stimulate proliferation and migration of endothelial cells than clinically well-established red light therapy. Further studies have to focus on intracellular mechanisms induced by different wavelengths in order to optimize this promising therapy in tissue regeneration. Nature Publishing Group UK 2017-09-06 /pmc/articles/PMC5587748/ /pubmed/28878330 http://dx.doi.org/10.1038/s41598-017-11061-y Text en © The Author(s) 2017 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/.
spellingShingle Article
Rohringer, Sabrina
Holnthoner, Wolfgang
Chaudary, Sidrah
Slezak, Paul
Priglinger, Eleni
Strassl, Martin
Pill, Karoline
Mühleder, Severin
Redl, Heinz
Dungel, Peter
The impact of wavelengths of LED light-therapy on endothelial cells
title The impact of wavelengths of LED light-therapy on endothelial cells
title_full The impact of wavelengths of LED light-therapy on endothelial cells
title_fullStr The impact of wavelengths of LED light-therapy on endothelial cells
title_full_unstemmed The impact of wavelengths of LED light-therapy on endothelial cells
title_short The impact of wavelengths of LED light-therapy on endothelial cells
title_sort impact of wavelengths of led light-therapy on endothelial cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5587748/
https://www.ncbi.nlm.nih.gov/pubmed/28878330
http://dx.doi.org/10.1038/s41598-017-11061-y
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