Hebei Key Laboratory of Stomatology, Department of Periodontology (II), Hebei Clinical Research Center for Oral Diseases, School and Hospital of Stomatology, Hebei Medical University, Zhongshan East Road 383, Shijiazhuang, 050017, Hebei, People's Republic of China.
Hebei Key Laboratory of Stomatology, Department of Laser Medicine, Hebei Clinical Research Center for Oral Diseases, School and Hospital of Stomatology, Hebei Medical University, Shijiazhuang, 050017, Hebei, People's Republic of China.
BMC Oral Health. 2023 Jul 19;23(1):501. doi: 10.1186/s12903-023-03132-6.
The key to the success of endogenous regeneration is to improve the homing rate of stem cells, and low-energy laser is an effective auxiliary means to promote cell migration and proliferation. The purpose of this study was to observe whether low-energy neodymium (Nd: YAG) laser with appropriate parameters can affect the proliferation and migration of periodontal ligament stem cells (PDLSCs) through SDF-1/CXCR4 pathway.
h PDLSCs were cultured and identified. CCK8 assay was used to detect the proliferation of h PDLSCs after different power (0, 0.25, 0.5, 1, and 1.5 W) Nd: YAG laser (MSP, 10 Hz, 30 s, 300 μ m) irradiation at 2th, 3rd,5th, and 7th days, and the optimal laser irradiation parameters were selected for subsequent experiments. Then, the cells were categorized into five groups: control group (C), SDF-1 group (S), AMD3100 group (A), Nd: YAG laser irradiation group (N), and Nd: YAG laser irradiation + AMD3100 group (N + A). the migration of h PDLSCs was observed using Transwell, and the SDF-1 expression was evaluated using ELISA andRT-PCR. The SPSS Statistics 21.0 software was used for statistical analysis.
The fibroblasts cultured were identified as h PDLSCs. Compared with the C, when the power was 1 W, the proliferation rate of h PDLSCs was accelerated (P < 0.05). When the power was 1.5 W, the proliferation rate decreased (P < 0.05). When the power was 0.25 and 0.5 W, no statistically significant difference in the proliferation rate was observed (P > 0.05). The number of cell perforations values as follows: C (956.5 ± 51.74), A (981.5 ± 21.15), S (1253 ± 87.21), N (1336 ± 48.54), and N + A (1044 ± 22.13), that increased significantly in group N (P < 0.05), but decreased in group N + A (P < 0.05). The level of SDF-1 and the expression level of SDF-1 mRNA in groups N and N + A was higher than that in group C (P < 0.05) but lower than that in group A (P < 0.05).
Nd: YAG laser irradiation with appropriate parameters provides a new method for endogenous regeneration of periodontal tissue. SDF-1/CXCR4 signaling pathway may be the mechanism of LLLT promoting periodontal regeneration.
内源性再生的关键在于提高干细胞的归巢率,低能量激光是促进细胞迁移和增殖的有效辅助手段。本研究旨在观察适当参数的低能量钕(Nd:YAG)激光是否通过 SDF-1/CXCR4 途径影响牙周膜干细胞(PDLSCs)的增殖和迁移。
培养并鉴定 hPDLSCs。CCK8 检测不同功率(0、0.25、0.5、1 和 1.5 W)Nd:YAG 激光(MSP,10 Hz,30 s,300 μm)照射 2、3、5 和 7 天后 hPDLSCs 的增殖情况,选择最佳激光照射参数进行后续实验。然后,将细胞分为五组:对照组(C)、SDF-1 组(S)、AMD3100 组(A)、Nd:YAG 激光照射组(N)和 Nd:YAG 激光照射+AMD3100 组(N+A)。使用 Transwell 观察 hPDLSCs 的迁移,ELISA 和 RT-PCR 评估 SDF-1 的表达。采用 SPSS Statistics 21.0 软件进行统计分析。
培养的成纤维细胞被鉴定为 hPDLSCs。与 C 组相比,当功率为 1 W 时,hPDLSCs 的增殖速度加快(P<0.05)。当功率为 1.5 W 时,增殖速度下降(P<0.05)。当功率为 0.25 和 0.5 W 时,增殖率无统计学差异(P>0.05)。细胞穿孔数分别为:C(956.5±51.74)、A(981.5±21.15)、S(1253±87.21)、N(1336±48.54)和 N+A(1044±22.13),N 组显著增加(P<0.05),但 N+A 组减少(P<0.05)。N 组和 N+A 组的 SDF-1 水平和 SDF-1mRNA 表达水平均高于 C 组(P<0.05),但低于 A 组(P<0.05)。
适当参数的 Nd:YAG 激光照射为牙周组织的内源性再生提供了一种新方法。SDF-1/CXCR4 信号通路可能是 LLLT 促进牙周再生的机制。