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Laser irradiation did not increase the proliferation or the differentiation of stem cells from normal and inflamed dental pulp

机译:激光照射不会增加正常和发炎的牙髓中干细胞的增殖或分化

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Objective: Low-level laser therapy (LLLT) has been reported to be responsible for promoting photostimulatory and photobiomodulatory effects in vivo and in vitro, stimulating cell growth, increasing cell metabolism, improving cell regeneration and invoking an anti-inflammatory response. This study was performed in order to investigate whether low-level laser therapy could increase the proliferation and differentiation potentials of hDPSC isolated from healthy dental pulps and from inflamed pulps. Design: Human dental pulp stem cells (hDPSC) were isolated from normal and inflamed dental pulps from different patients. STRO-1-positive cells were isolated and irradiated with a red low-level laser (660 nm) in four different energy fluences (0.05, 0.30, 7 and 42 J/cm 2); the authors hypothesized that the first three fluences would promote biostimulatory effects, whereas the highest dose would induce antiproliferative effects. The two lower fluences were produced by irradiating the two higher fluences through a dentine disc, which was used to simulate a clinical condition. The proliferation and the cell odonto-osteogenic differentiation competence were compared. Results: No statistically significant differences were observed between the proliferation rates and the relative productions of mineralized nodules compared to the respective controls, either for hDPSC from normal or inflamed dental pulps. Conclusions: The irradiation with low-level InGaAlP red low-level laser (660 nm) in four different energy fluences (0.05, 0.30, 7 and 42 J/cm 2) potentiated neither proliferation nor odonto-osteogenic differentiation of hDPSC isolated from patients with normal and inflamed pulps.
机译:目的:据报道,低水平激光疗法(LLLT)可以在体内和体外促进光刺激和光生物调节作用,刺激细胞生长,增加细胞代谢,改善细胞再生并引发抗炎反应。进行这项研究是为了研究低水平激光疗法是否可以增加从健康牙髓和发炎牙髓中分离出的hDPSC的增殖和分化潜能。设计:从不同患者的正常牙髓和发炎牙髓中分离出人牙髓干细胞(hDPSC)。分离STRO-1阳性细胞,并用红色低能激光(660 nm)以四种不同的能量通量(0.05、0.30、7和42 J / cm 2)辐照;作者假设前三个注量会促进生物刺激作用,而最高剂量会诱导抗增殖作用。这两种较低的注量是通过用牙本质盘照射两种较高的注量来产生的,该牙本质盘用于模拟临床状况。比较了增殖和细胞成骨细胞分化能力。结果:与正常对照组或发炎的牙髓中的hDPSC相比,与相应的对照组相比,矿化结节的增殖速率和相对产量之间没有观察到统计学上的显着差异。结论:在4种不同能量通量(0.05、0.30、7和42 J / cm 2)下,用InGaAlP红色低能级激光(660 nm)辐照,既不会增强hDPSC的增殖,也不会促进其成牙分化。正常和发炎的牙髓。

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