University of Pavia, Department of Molecular Medicine, Biochemistry Unit "A.Castellani," INSTM UdR of Pavia, 27100 Pavia, ItalyeUniversity of Pavia, Interdipartimental Center for Tissue Engineering (CIT), 27100 Pavia, Italy.
University of Pavia, Department of Public Health, Experimental Medicine and Forensics, 27100 Pavia, ItalyeUniversity of Pavia, Interdipartimental Center for Tissue Engineering (CIT), 27100 Pavia, Italy.
J Biomed Opt. 2013 Dec;18(12):128006. doi: 10.1117/1.JBO.18.12.128006.
Several studies have shown that low-level laser irradiation (LLLI) has beneficial effects on bone regeneration. The objective of this study was to examine the in vitro effects of LLLI on proliferation and differentiation of a human osteoblast-like cell line (Saos-2 cell line). Cultured cells were exposed to different doses of LLLI with a semiconductor diode laser (659 nm; 10 mW power output). The effects of laser on proliferation were assessed daily up to seven days of culture in cells irradiated once or for three consecutive days with laser doses of 1 or 3 J/cm(2). The obtained results showed that laser stimulation enhances the proliferation potential of Saos-2 cells without changing their telomerase pattern or morphological characteristics. The effects on cell differentiation were assessed after three consecutive laser irradiation treatments in the presence or absence of osteo-inductive factors on day 14. Enhanced secretion of proteins specific for differentiation toward bone as well as calcium deposition and alkaline phosphatase activity were observed in irradiated cells cultured in a medium not supplemented with osteogenic factors. Taken together these findings indicate that laser treatment enhances the in vitro proliferation of Saos-2 cells, and also influences their osteogenic maturation, which suggest it is a helpful application for bone tissue regeneration.
几项研究表明,低水平激光照射(LLLI)对骨再生有有益的影响。本研究的目的是研究体外低水平激光照射对人成骨样细胞系(Saos-2 细胞系)增殖和分化的影响。将培养的细胞暴露于半导体二极管激光(659nm;10mW 功率输出)的不同剂量下。在照射一次或连续照射三天的激光剂量为 1 或 3J/cm2的情况下,评估了激光对增殖的影响,培养时间长达 7 天。结果表明,激光刺激增强了 Saos-2 细胞的增殖潜力,而不会改变其端粒酶模式或形态特征。在第 14 天,在存在或不存在成骨诱导因子的情况下,对连续三次激光照射处理后的细胞分化进行了评估。在未补充成骨因子的培养基中培养的照射细胞中,观察到对骨分化特异的蛋白质的增强分泌、钙沉积和碱性磷酸酶活性。这些发现表明,激光处理增强了 Saos-2 细胞的体外增殖,并且还影响其成骨成熟,这表明它是一种有助于骨组织再生的应用。
Beijing Da Xue Xue Bao Yi Xue Ban. 2017-4-18
Photomed Laser Surg. 2005-4
J Biomed Opt. 2013-12
J Photochem Photobiol B. 2016-2
Int J Mol Sci. 2021-10-13
Aesthetic Plast Surg. 2021-8
Int J Mol Sci. 2020-11-26