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Effects of Low-Level Er:YAG Laser Irradiation on Proliferation and Calcification of Primary Osteoblast-Like Cells Isolated From Rat Calvaria

机译:低级ER的影响:YAG激光辐照对大鼠CALVARIA分离的原发性成骨细胞增殖和钙化的影响

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摘要

Several reports have shown that the photo-bio-modulation of cells by various lasers has favorable biological effects. However, the effects of low-level Er:YAG laser irradiation on osteoblasts remain unclear. The purpose of this study was to evaluate the effects of low-level Er:YAG laser irradiation on proliferation and osteogenic differentiation of primary osteoblast-like cells isolated from the calvariae of 3–5-day-old Wistar rats. Cells were irradiated by Er:YAG laser at energy fluences of 2.2, 3.3, and 4.3 J/cm2, respectively. After irradiation, cell surface temperatures were measured and cell proliferation was evaluated by flow cytometry and CCK-8. Calcification was evaluated by measuring areas of Alizarin red S staining after 7, 14, and 21 days culture in osteoinductive medium. Gene expression in non-irradiated and laser-irradiated cells was evaluated by qPCR at 3, 6, and 12 h, as well as 1, 3, 7, and 14 days after irradiation. Microarray analysis was performed to comprehensively evaluate the gene expression of non-irradiated and irradiated cells at 3.3 J/cm2 at 6 h after irradiation. No pronounced increase of cell surface temperature was induced by irradiation. Irradiation did not affect osteoblast-like cell proliferation. Osteoblast-like cell calcification was significantly increased 7 days after Er:YAG laser irradiation at 3.3 J/cm2. Bglap expression was significantly increased in cells irradiated at 3.3 J/cm2 6 h post-irradiation. Microarray analysis showed that irradiation at 3.3 J/cm2 caused an upregulation of inflammation-related genes and downregulation of Wisp2. Gene set enrichment analysis also clarified enrichment of inflammation-related and Notch signaling gene sets. In conclusion, low-level Er:YAG laser irradiation at 3.3 J/cm2 enhanced calcification of primary osteoblast-like cells via enhanced Bglap expression and enriched Notch signaling.
机译:有几个报告表明,各种激光器的细胞的光生物调制具有良好的生物效应。然而,低级ER的影响:对成骨细胞的YAG激光照射仍然不清楚。本研究的目的是评估低水平ER的影响:YAG激光辐照对从3-5天的Wistar大鼠的Calvariae分离的原发性成骨细胞样细胞的增殖和成骨分化。通过ER:ER的细胞照射:YAG激光的能量流量分别为2.2,3.3和4.3J / cm2。在照射后,测量细胞表面温度,通过流式细胞术和CCK-8评价细胞增殖。通过在骨诱导培养基中7,14和21天培养后的茜素红S染色的施用区域来评估钙化。通过Q,6和12小时的QPCR评估非照射和激光辐照细胞中的基因表达,以及照射后的1,3,7和14天。进行微阵列分析以在照射后6小时在3.3J / cm 2下综合评价非照射和辐照细胞的基因表达。通过照射诱导细胞表面温度的明显增加。辐射不影响成骨细胞样细胞增殖。 ER后7天的成骨细胞样细胞钙化显着增加:YAG激光照射在3.3J / cm2。在照射后照射3.3J / cm2 6 H照射的细胞中,Bglap表达显着增加。微阵列分析表明,3.3J / cm2的照射导致炎症相关基因的上调和智能的下调。基因设定浓缩分析还澄清了炎症相关和Notch信号基因集的富集。总之,低水平ER:YAG激光照射在3.3J / cm2通过增强的BGLAP表达和富集的NOTCH信号传导增强初级成骨细胞样细胞的钙化。

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