Department of Biological Sciences, Bauru School of Dentistry, University of São Paulo, Bauru, SP, Brazil.
Departamento de Física e Ciência dos Materiais, Instituto de Física de São Carlos, Universidade de São Paulo, São Carlos, SP, Brazil.
J Photochem Photobiol B. 2017 Apr;169:35-40. doi: 10.1016/j.jphotobiol.2017.02.020. Epub 2017 Feb 28.
Low level laser therapy (LLLT) has been shown to stimulate bone cell metabolism but their impact on the matrix metalloproteinase (MMP) expression and activity is little explored. This study evaluated the influence of LLLT at two different wavelengths, red and infrared, on MC3T3-E1 preosteoblast viability, alkaline phosphatase (ALP) and MMP-2 and -9 activities. To accomplish this, MC3T3-E1 cells were irradiated with a punctual application of either red (660nm; InGaAIP active medium) or infrared (780nm; GaAlAs active medium) lasers both at a potency of 20mW, energy dose of 0.08 or 0.16J, and energy density of 1.9J/cm or 3.8J/cm, respectively. The control group received no irradiation. Cellular viability, ALP and MMP-2 and -9 activities were assessed by MTT assay, enzymatic activity and zymography, respectively, at 24, 48 and 72h. The treatment of cells with both red and infrared lasers significantly increased the cellular viability compared to the non-irradiated control group at 24 and 48h. The ALP activity was also up modulated in infrared groups at 24 and 72h, depending on the energy densities. In addition, the irradiation with red laser at the energy density of 1.9J/cm promoted an enhancement of MMP-2 activity at 48 and 72h. However, no differences were observed for the MMP-9 activity. In conclusion, when used at these specific parameters, LLL modulates both preosteoblast viability and differentiation highlighted by the increased ALP and MMP-2 activities induced by irradiation.
低水平激光疗法 (LLLT) 已被证明可刺激骨细胞代谢,但它们对基质金属蛋白酶 (MMP) 表达和活性的影响尚未得到充分探索。本研究评估了两种不同波长的 LLLT(红色和红外线)对 MC3T3-E1 前成骨细胞活力、碱性磷酸酶 (ALP) 和 MMP-2 和 -9 活性的影响。为此,使用红色 (660nm;InGaAIP 有源介质) 或红外线 (780nm;GaAlAs 有源介质) 激光分别对 MC3T3-E1 细胞进行点状照射,激光强度为 20mW,能量剂量为 0.08 或 0.16J,能量密度分别为 1.9J/cm 或 3.8J/cm。对照组未接受照射。通过 MTT 测定法分别在 24、48 和 72 小时评估细胞活力、ALP 和 MMP-2 和 -9 活性,通过酶活性和酶谱法评估。与未照射的对照组相比,两种红色和红外线激光处理细胞在 24 和 48 小时时显著增加了细胞活力。在 24 和 72 小时时,红外组的 ALP 活性也上调,这取决于能量密度。此外,红色激光在 1.9J/cm 的能量密度下照射可在 48 和 72 小时时促进 MMP-2 活性的增强。然而,MMP-9 活性没有差异。总之,在这些特定参数下使用时,LLLT 可调节前成骨细胞活力和分化,这突出表现在照射诱导的 ALP 和 MMP-2 活性增加。