Red (635 nm), Near-Infrared (808 nm) and Violet-Blue (405 nm) Photobiomodulation Potentiality on Human Osteoblasts and Mesenchymal Stromal Cells: A Morphological and Molecular In Vitro Study.
Red (635 nm), Near-Infrared (808 nm) and Violet-Blue (405 nm) Photobiomodulation Potentiality on Human Osteoblasts and Mesenchymal Stromal Cells: A Morphological and Molecular In Vitro Study.
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DOI:
10.3390/ijms19071946
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发表时间:
2018-07-03
影响因子:
5.6
通讯作者:
Sassoli C
中科院分区:
文献类型:
--
作者:
Tani A;Chellini F;Giannelli M;Nosi D;Zecchi-Orlandini S;Sassoli C
Photobiomodulation (PBM) has been used for bone regenerative purposes in different fields of medicine and dentistry, but contradictory results demand a skeptical look for its potential benefits. This in vitro study compared PBM potentiality by red (635 ± 5 nm) or near-infrared (NIR, 808 ± 10 nm) diode lasers and violet-blue (405 ± 5 nm) light-emitting diode operating in a continuous wave with a 0.4 J/cm2 energy density, on human osteoblast and mesenchymal stromal cell (hMSC) viability, proliferation, adhesion and osteogenic differentiation. PBM treatments did not alter viability (PI/Syto16 and MTS assays). Confocal immunofluorescence and RT-PCR analyses indicated that red PBM (i) on both cell types increased vinculin-rich clusters, osteogenic markers expression (Runx-2, alkaline phosphatase, osteopontin) and mineralized bone-like nodule structure deposition and (ii) on hMSCs induced stress fiber formation and upregulated the expression of proliferation marker Ki67. Interestingly, osteoblast responses to red light were mediated by Akt signaling activation, which seems to positively modulate reactive oxygen species levels. Violet-blue light-irradiated cells behaved essentially as untreated ones and NIR irradiated ones displayed modifications of cytoskeleton assembly, Runx-2 expression and mineralization pattern. Although within the limitations of an in vitro experimentation, this study may suggest PBM with 635 nm laser as potential effective option for promoting/improving bone regeneration.
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影响因子:
12.4
作者:
Chen Q;Shou P;Zheng C;Jiang M;Cao G;Yang Q;Cao J;Xie N;Velletri T;Zhang X;Xu C;Zhang L;Yang H;Hou J;Wang Y;Shi Y
通讯作者:
Shi Y
影响因子:
2.1
作者:
Chellini, Flaminia;Giannelli, Marco;Sassoli, Chiara
通讯作者:
Sassoli, Chiara
影响因子:
2.1
作者:
Ates, Gamze Bolukbasi;Can, Ayse Ak;Gulsoy, Murat
通讯作者:
Gulsoy, Murat
影响因子:
2.4
作者:
Chen, Chung-Huang;Hung, Huey-Shan;Hsu, Shan-Hui
通讯作者:
Hsu, Shan-Hui
影响因子:
2.4
作者:
Chellini, Flaminia;Sassoli, Chiara;Giannelli, Marco
通讯作者:
Giannelli, Marco