Pansani Taisa Nogueira, Basso Fernanda Gonçalves, Turrioni Ana Paula Silveira, Soares Diana Gabriela, Hebling Josimeri, de Souza Costa Carlos Alberto
Department of Dental Materials and Prosthodontics, Araraquara School of Dentistry, University Estadual Paulista (UNESP), Araraquara, Brazil.
Department of Orthodontics and Pediatric Dentistry, Araraquara School of Dentistry, University Estadual Paulista (UNESP), Araraquara, Brazil.
Lasers Med Sci. 2017 Jan;32(1):45-52. doi: 10.1007/s10103-016-2081-x. Epub 2016 Sep 27.
This study evaluated the effects of low-level laser therapy (LLLT) and epidermal growth factor (EGF) on fibroblasts obtained from young and elderly individuals. Gingival fibroblasts from young (Y) and elderly (E) individuals were seeded in wells of 24-well plates with Dulbecco's modified Eagle's medium (DMEM) containing 10 % of fetal bovine serum (FBS). After 24 h, the cells were irradiated (LASERTable-InGaAsP-780 ± 3 nm, 25 mW, 3 J/cm) or exposed to EGF (100 μM). After 72 h, cells were evaluated for viability, migration, collagen and vascular endothelial growth factor (VEGF) synthesis, and gene expression of growth factors. Data were analyzed by Kruskal-Wallis and Mann-Whitney tests (α = 5 %). Y and E fibroblasts irradiated with laser or exposed to EGF showed increased viability and collagen synthesis. Enhanced cell migration was observed for Y fibroblasts after both treatments, whereas only the LLLT stimulated migration of E cells. VEGF synthesis was higher for Y and E cells exposed to EGF, while this synthesis was reduced when E fibroblasts were irradiated. Increased gene expression of VEGF was observed only for Y and E fibroblasts treated with LLLT. Regardless of a patient's age, the LLLT and EGF applications can biostimulate gingival fibroblast functions involved in tissue repair.
本研究评估了低强度激光疗法(LLLT)和表皮生长因子(EGF)对从年轻人和老年人获取的成纤维细胞的影响。将来自年轻(Y)和老年(E)个体的牙龈成纤维细胞接种于含有10%胎牛血清(FBS)的杜尔贝科改良伊格尔培养基(DMEM)的24孔板孔中。24小时后,对细胞进行照射(LASERTable-InGaAsP-780±3纳米,25毫瓦,3焦耳/平方厘米)或暴露于EGF(100微摩尔)。72小时后,评估细胞的活力、迁移、胶原蛋白和血管内皮生长因子(VEGF)合成以及生长因子的基因表达。数据采用克鲁斯卡尔-沃利斯检验和曼-惠特尼检验进行分析(α=5%)。用激光照射或暴露于EGF的Y和E成纤维细胞显示活力和胶原蛋白合成增加。两种处理后,Y成纤维细胞均观察到细胞迁移增强,而仅LLLT刺激E细胞迁移。暴露于EGF的Y和E细胞的VEGF合成较高,而E成纤维细胞经照射后该合成减少。仅在用LLLT处理的Y和E成纤维细胞中观察到VEGF基因表达增加。无论患者年龄如何,LLLT和EGF应用均可对参与组织修复的牙龈成纤维细胞功能进行生物刺激。