Key Laboratory of Shaanxi Province for Craniofacial Precision Medicine Research, College of Stomatology, Xi'an Jiaotong University, Xi'an, Shaanxi, China.
Clinical Research Center of Shaanxi Province for Dental and Maxillofacial Diseases, College of Stomatology, Xi'an Jiaotong University, Xi'an, Shaanxi, China.
Lasers Med Sci. 2022 Dec;37(9):3591-3599. doi: 10.1007/s10103-022-03638-5. Epub 2022 Sep 15.
Periodontitis often causes damage to the periodontal tissue and affects the function of human periodontal ligament stem cells (hPDLSCs). Low-level laser therapy (LLLT) has been used for periodontal treatment and can upregulate the proliferation and osteogenesis of hPDLSCs. The purpose of this study was to investigate the effects of LLLT on the proliferation, osteogenic differentiation, inflammatory reaction, and oxidative stress of hPDLSCs in an inflammatory environment (pPDLSCs). We designed one control group and three testing groups (treated with Nd:YAG laser at 4, 8, and 16 J/cm) of hPDLSCs from periodontitis patients who were diagnosed with stable phase periodontitis. Cell proliferation was measured by colony-forming unit fibroblast (CFU-F) assays and 3-(4,5-dimethylthiazol-2yl)-2,5-diphenyltetrazolium bromide (MTT) assays. The osteogenic capacity of the cells was determined by alkaline phosphatase (ALP) staining, ALP activity assays, Alizarin Red S staining and the mRNA transcript levels of runt-related transcription factor 2 (Runx2), ALP, and osteocalcin (OCN). The effects of LLLT on the secretion of tumor necrosis factor-α (TNF-α) and interleukin (IL)-1β by PDLSCs were measured by enzyme-linked immunosorbent assay (ELISA). We also evaluated the oxidative stress of hPDLSCs and pPDLSCs by measuring the reactive oxygen species (ROS) level, malondialdehyde (MDA) level, and superoxide dismutase (SOD) activity after treatment with LLLT at 4, 8, and 16 J/cm. Our results demonstrated that LLLT could modulate the osteogenic potential of pPDLSCs at 8 J/cm. Inflammatory stimuli induced excess ROS release, and LLLT at 4-8 J/cm promoted oxidative stress levels in hPDLSCs but decreased the expression of inflammatory cytokines and ROS levels in pPDLSCs. Moreover, LLLT at 16 J/cm could significantly suppress proliferation and osteogenic differentiation and promote inflammatory cytokines and ROS levels in pPDLSCs. In conclusion, LLLT could regulate proliferation, osteogenesis, inflammatory reaction, and oxidative stress of human periodontal ligament stem cells under inflammatory conditions.
牙周炎常导致牙周组织损伤,并影响人牙周韧带干细胞(hPDLSCs)的功能。低水平激光疗法(LLLT)已用于牙周治疗,可上调 hPDLSCs 的增殖和成骨分化。本研究旨在探讨 LLLT 对牙周炎患者来源的 hPDLSCs(pPDLSCs)在炎症环境下的增殖、成骨分化、炎症反应和氧化应激的影响。我们设计了一个对照组和三个实验组(用 Nd:YAG 激光处理,激光能量密度分别为 4、8 和 16 J/cm²),实验组的细胞均来自牙周炎患者。采用集落形成单位成纤维细胞(CFU-F)实验和 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)实验来检测细胞增殖。通过碱性磷酸酶(ALP)染色、ALP 活性测定、茜素红 S 染色和 runt 相关转录因子 2(Runx2)、ALP 和骨钙素(OCN)的 mRNA 转录水平来检测细胞的成骨能力。通过酶联免疫吸附测定(ELISA)检测 LLLT 对 PDLSCs 分泌肿瘤坏死因子-α(TNF-α)和白细胞介素(IL)-1β的影响。我们还通过测量 LLLT 在 4、8 和 16 J/cm²处理后 hPDLSCs 和 pPDLSCs 的活性氧(ROS)水平、丙二醛(MDA)水平和超氧化物歧化酶(SOD)活性来评估 hPDLSCs 和 pPDLSCs 的氧化应激。结果表明,LLLT 可在 8 J/cm²调节 pPDLSCs 的成骨潜能。炎症刺激诱导过量的 ROS 释放,4-8 J/cm²的 LLLT 促进 hPDLSCs 的氧化应激水平,但降低 pPDLSCs 中炎症细胞因子和 ROS 水平的表达。此外,16 J/cm²的 LLLT 可显著抑制 pPDLSCs 的增殖和成骨分化,并促进 pPDLSCs 中炎症细胞因子和 ROS 水平的升高。总之,LLLT 可调节炎症条件下人牙周韧带干细胞的增殖、成骨分化、炎症反应和氧化应激。