3.9 Article

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

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PHOTOMEDICINE AND LASER SURGERY
卷 36, 期 2, 页码 83-91

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MARY ANN LIEBERT, INC
DOI: 10.1089/pho.2017.4344

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photobiomodulation; high-intensity laser therapy; Nd:YAG; equine mesenchymal stem cells; IL-10; VEGF

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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 1064nm 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 1064nm irradiation with an energy density of 9.77J/cm(2) and a mean output power of 13.0W for 10sec. MSC viability and proliferation were evaluated through flow cytometry and real-time live cell analysis. Gene expression and cytokine production in the first 24h 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 1064nm irradiation shows promise in the photobiomodulation of MSCs to enhance their therapeutic properties.

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