Department of Physiology and Pathology, Araraquara School of Dentistry, UNESP, R. Humaita, 1680, Araraquara, SP, Brazil.
Department of Pediatric Dentistry, Araraquara School of Dentistry, UNESP, Araraquara, SP, Brazil.
Lasers Med Sci. 2020 Jul;35(5):1205-1212. doi: 10.1007/s10103-020-02974-8. Epub 2020 Feb 7.
The aim of this study was to assess the effects of IL-6 and IL-8 cytokines on human gingival fibroblasts (HGF) cultured in a 3-D model and the possible photobiomodulation (PBM) of such effects by low-level laser therapy. In complete culture medium (DMEM), HGF from a healthy patient were seeded in a type I collagen matrix inserted into 24-well plates. After 5 days of incubation, the cytokines were added or not to serum-free DMEM, which was applied to the cell-enriched matrices. Then, PBM was performed: three consecutive irradiations using LaserTable diode device (780 nm, 0.025 W) at 0.5 J/cm were delivered or not to the cells. Twenty-four hours after the last irradiation, cell viability and morphology, gene expression, and synthesis of inflammatory cytokines and growth factors were assessed. The histological evaluation demonstrated that, for all groups, matrices presented homogeneous distribution of cells with elongated morphology. However, numerous cytokine-exposed cells were rounded. IL-6 and IL-8 decreased cell viability, synthesis of VEGF, and gene expression of collagen type I. PBM enhanced cell density in the matrices and stimulated VEGF expression, even after IL-6 challenge. Reduced TNF-α synthesis occurred in those cells subjected to PBM. In conclusion, PBM can penetrate collagen matrix and stimulate HGF, highlighting the relevance of this research model for further phototherapy studies and in vitro biomodulation of the healing process.
本研究旨在评估白细胞介素-6(IL-6)和白细胞介素-8(IL-8)细胞因子对三维模型中培养的人牙龈成纤维细胞(HGF)的影响,以及低水平激光疗法(PBM)对这些影响的可能光生物调节作用。在完全培养基(DMEM)中,将来自健康患者的 HGF 接种到插入 24 孔板的 I 型胶原基质中。孵育 5 天后,向无血清 DMEM 中添加或不添加细胞因子,然后将其应用于富含细胞的基质。然后进行 PBM:使用 LaserTable 二极管设备(780nm,0.025W)连续进行三次照射,每次照射 0.5J/cm,或不对细胞进行照射。最后一次照射后 24 小时,评估细胞活力和形态、基因表达以及炎症细胞因子和生长因子的合成。组织学评估表明,对于所有组,基质均呈现出细胞均匀分布和伸长形态。然而,许多暴露于细胞因子的细胞呈圆形。IL-6 和 IL-8 降低了细胞活力、VEGF 的合成和 I 型胶原的基因表达。PBM 增强了基质中细胞的密度,并刺激了 VEGF 的表达,即使在受到 IL-6 挑战后也是如此。那些接受 PBM 的细胞中 TNF-α 的合成减少。总之,PBM 可以穿透胶原基质并刺激 HGF,这突出了该研究模型在进一步的光疗研究和体外生物调节愈合过程中的重要性。