Oral& Maxillofacial Diseases Research Center, Faculty of Dentistry, Mashhad University of Medical Sciences, Mashhad, Iran.
Pharmaceutical Research Center, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran.
Iran J Basic Med Sci. 2013 Oct;16(10):1071-4.
OBJECTIVE(S): Recent investigations show that both proliferation and secretion of macromolecules by cells can be regulated by low level laser therapy (LLLT). The aim of this study was to determine whether LLLT could induce a bio-stimulatory effects on human gingival fibroblasts (HGF3-PI 53). Therefore, the effect of laser irradiation on human gingival cell proliferation and collagen type I gene expression was studied.
HGF3-PI 53 were cultured in 96-well plate and then irradiated with LLLT gallium-aluminum-arsenide (Ga-Al-As), 810 nm, 50 mW diode laser (energy: 4 J/cm(2)) for three consecutive days. The cell proliferation was measured on days 1, 2 and 3 after irradiation with LLLT using MTT assay. Real time PCR analysis was utilized on day 3 to evaluate the expression of collagen type I gene. Results : Evaluation of cellular proliferation, one day after laser treatment showed no difference compared to control group. But on days 2 and 3, significant increase in proliferation was observed in the irradiated cell populations in comparison to the control group. Treatment of HGF3-PI 53 by laser resulted in a significant increase in collagen I gene expression on 3 day.
The results demonstrated that LLLT stimulated human gingival fibroblast proliferation as well as collagen type I gene expression in vitro.
最近的研究表明,细胞的增殖和大分子分泌均可受到低水平激光治疗(LLLT)的调节。本研究旨在确定 LLLT 是否能对人牙龈成纤维细胞(HGF3-PI 53)产生生物刺激作用。因此,研究了激光照射对人牙龈细胞增殖和 I 型胶原基因表达的影响。
将 HGF3-PI 53 培养在 96 孔板中,然后用 810nm、50mW 砷化镓铝二极管激光(能量:4J/cm2)连续照射 3 天。用 MTT 法在激光照射后第 1、2 和 3 天测量细胞增殖。第 3 天用实时 PCR 分析评估 I 型胶原基因的表达。
激光处理后第 1 天,细胞增殖的评估与对照组无差异。但在第 2 和第 3 天,与对照组相比,照射细胞群的增殖明显增加。激光处理 HGF3-PI 53 导致 I 型胶原基因表达在第 3 天显著增加。
结果表明,LLLT 刺激人牙龈成纤维细胞增殖以及体外 I 型胶原基因表达。