近红外激光对牙周韧带干细胞的光生物调节作用。

Mohammd Ayyoub Rigi-Ladez, S. S. Hendi, Alireza Mirzaei, L. Gholami, R. Fekrazad
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摘要

目的观察波长810 nm和940 nm近红外二极管激光器不同能量密度对牙周韧带源性干细胞(PDLSCs)增殖和存活的影响。方法分离和鉴定后,将PDLSCs培养于透明的96孔板。每口井分别用810 nm (L1)或940 nm (L2)激光照射,能量密度分别为0.5、1.5和2.5 J/cm2,输出功率为100 mW。未辐照井作为对照。采用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基- 2h -溴化四氮唑(MTT)法测定照射后24小时细胞活力,采用台盼蓝染色和计数法测定照射后24、48和72小时细胞增殖。碘化丙啶(PI)染色检测辐照72小时后是否有核固缩或核碎裂。结果仅在能量密度为2.5 J/cm2的940 nm激光照射组细胞活力增加(P < 0.001)。能量密度为2.5 J/cm2的940 nm激光照射组在各时间点细胞增殖均显著高于其他组(P < 0.001)。PI染色各组细胞核未见明显变化。结论能量密度为2.5 J/cm2的940 nm激光照射PDLSCs可促进细胞高效增殖。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Near Infrared Laser Photobiomodulation of Periodontal Ligament Stem Cells.
OBJECTIVE To determine the effect of different energy densities of near infrared diode lasers with wavelengths of 810 or 940 nm on the proliferation and survival of periodontal ligament derived stem cells (PDLSCs). METHODS After isolation and characterisation, PDLSCs were cultured in clear 96-well plates. Each well was irradiated by either 810 nm (L1) or 940 nm (L2) lasers, with energy densities of 0.5, 1.5 and 2.5 J/cm2 and an output power of 100 mW. A non-irradiated well was used as a control. Cellular viability was measured 24 hours after irradiation using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay and proliferation was measured 24, 48 and 72 hours after irradiation using trypan blue staining and counting. Propidium iodide (PI) staining was used to identify any pyknotic nuclei or nuclear fragmentation 72 hours after irradiation. RESULTS An increase in viability was observed only in the group with the 940 nm laser irradiation at energy density of 2.5 J/cm2 (P < 0.001). The proliferation of cells was significantly increased in the group with 940 nm laser irradiation at energy density of 2.5 J/cm2 at all the time points examined in comparison to other groups (P < 0.001). PI staining showed no change in cell nuclei in any of the groups. CONCLUSION Irradiation of PDLSCs with a 940 nm laser at an energy density of 2.5 J/cm2 could promote efficient cell proliferation.
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