Department of Laser Medicine, Chinese People's Liberation Army General Hospital, Beijing, China (mainland).
State Key Laboratory of Proteomics, National Center for Protein Sciences (Beijing), Beijing Institute of Lifeomics, Beijing, China (mainland).
Med Sci Monit. 2019 Nov 19;25:8744-8752. doi: 10.12659/MSM.920396.
BACKGROUND Photobiomodulation (PBM) has been explored as a promising therapeutic strategy to regulate bone cell growth; however, the effects of PBM on osteoblast cell lines remains poorly understood. In addition, as a light source of PBM, the light uniformity of light-emitting diode (LED) devices has not been given enough attention. MATERIAL AND METHODS Here, we sought to investigate the effects of PBM on MC3T3-E1 cells via 630 nm and 810 nm light from a newly designed LED with high uniformity of light. Cell proliferation, flow cytometric analysis, alkaline phosphatase (ALP) staining, ALP activity, Alizarin Red S staining, and quantitative real-time polymerase chain reaction (qRT-PCR) were carried out to assess treatment response. MC3T3-E1 cells were irradiated with LED devices (630±5 nm and 810±10 nm, continuous wave) for 200 seconds at a power density of 5 mW/cm² once daily. RESULTS Increases in cell proliferation and decreases in cell apoptosis were evident following irradiation. ALP staining intensity and activity were also significantly increased following irradiation. Level of mineralization was obviously enhanced in irradiated groups compared with non-irradiated controls. qRT-PCR also showed significant increases in mRNA expression of osteocalcin (OCN) and osteoprotegerin (OPG) in the irradiated groups. CONCLUSIONS Our results showed that LED PBM could promote the proliferation, ALP staining intensity and activity, level of mineralization, gene expression of OCN and OPG of MC3T3-E1 cells, with no significant difference between the 630 nm- and 810 nm-irradiated groups.
光生物调节(PBM)已被探索作为一种有前途的治疗策略,以调节骨细胞的生长;然而,PBM 对成骨细胞系的影响仍知之甚少。此外,作为 PBM 的光源,发光二极管(LED)设备的光均匀性尚未得到足够重视。
在这里,我们试图通过新设计的具有高均匀性的光的 630nm 和 810nm 光来研究 PBM 对 MC3T3-E1 细胞的影响。通过细胞增殖、流式细胞分析、碱性磷酸酶(ALP)染色、ALP 活性、茜素红 S 染色和定量实时聚合酶链反应(qRT-PCR)来评估治疗反应。MC3T3-E1 细胞用 LED 设备(630±5nm 和 810±10nm,连续波)照射 200 秒,功率密度为 5mW/cm²,每天一次。
细胞增殖增加,细胞凋亡减少。ALP 染色强度和活性也明显增加。与未照射对照组相比,照射组的矿化水平明显增强。qRT-PCR 还显示照射组骨钙素(OCN)和骨保护素(OPG)的 mRNA 表达明显增加。
我们的结果表明,LED PBM 可以促进 MC3T3-E1 细胞的增殖、ALP 染色强度和活性、矿化水平、OCN 和 OPG 的基因表达,630nm 和 810nm 照射组之间没有显著差异。