In Vitro Effects of High-Intensity Laser Photobiomodulation on Equine Bone Marrow-Derived Mesenchymal Stem Cell Viability and Cytokine Expression.

Autor:	Peat FJ; Orthopaedic Research Center, Colorado State University Veterinary Teaching Hospital , Fort Collins, Colorado., Colbath AC; Orthopaedic Research Center, Colorado State University Veterinary Teaching Hospital , Fort Collins, Colorado., Bentsen LM; Orthopaedic Research Center, Colorado State University Veterinary Teaching Hospital , Fort Collins, Colorado., Goodrich LR; Orthopaedic Research Center, Colorado State University Veterinary Teaching Hospital , Fort Collins, Colorado., King MR; Orthopaedic Research Center, Colorado State University Veterinary Teaching Hospital , Fort Collins, Colorado.
Jazyk:	angličtina
Zdroj:	Photomedicine and laser surgery [Photomed Laser Surg] 2018 Feb; Vol. 36 (2), pp. 83-91. Date of Electronic Publication: 2017 Nov 13.
DOI:	10.1089/pho.2017.4344
Abstrakt:	Objective: This study aimed to examine the influence of neodymium-doped yttrium aluminum garnet (Nd:YAG) laser irradiation on equine bone marrow-derived mesenchymal stem cell (MSC) viability, proliferation, and cytokine expression in vitro. Background: Photobiomodulation of cells using monochromatic light is a technique designed to influence cellular processes. Previous studies have shown dose-dependent effects of low-level laser irradiation on cell proliferation and cytokine expression in a range of cell types and species. Evidence for the influence of 1064 nm wavelength near-infrared irradiation on MSCs is sparse, and high-energy doses have shown inhibitory effects. Methods: MSC cultures from six horses were exposed to 1064 nm irradiation with an energy density of 9.77 J/cm 2 and a mean output power of 13.0 W for 10 sec. MSC viability and proliferation were evaluated through flow cytometry and real-time live cell analysis. Gene expression and cytokine production in the first 24 h after irradiation were analyzed through polymerase chain reaction (PCR), multiplex assay, and enzyme-linked immunosorbent assay. Results: No difference in viability was detected between irradiated and control MSCs. Irradiated cells demonstrated slightly lower proliferation rates, but remained within 3.5% confluence of control cells. Twenty-four hours after irradiation, irradiated MSCs demonstrated a significant increase in expression of interleukin (IL)-10 and vascular endothelial growth factor (VEGF) compared with control MSCs. Conclusions: Under these irradiation parameters, equine MSCs remained viable and expressed increased concentrations of IL-10 and VEGF. IL-10 has an anti-inflammatory action by inhibiting the synthesis of proinflammatory cytokines at the transcriptional level. This response to 1064 nm irradiation shows promise in the photobiomodulation of MSCs to enhance their therapeutic properties.
Databáze:	MEDLINE
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