Zhou Yan, Chen Qiang, Zhang Wantong, Ye Lin, Wang Yao
The Department of Preventive Dentistry, The Affiliated Stomatological Hospital, Southwest Medical University, Luzhou, 646000, China.
Luzhou Key Laboratory of Oral & Maxillofacial Reconstruction and Regeneration, Southwest Medical University, Luzhou, 646000, China.
Lasers Med Sci. 2025 Jan 28;40(1):52. doi: 10.1007/s10103-025-04303-3.
The purpose of this study was to examine how low-energy LED red light influences the early to middle stage of osteogenic differentiation of periodontal ligament stem cells (PDLSCs) via the ERK5 signaling pathway. METHODS: PDLSCs were extracted from periodontal membrane tissue using enzymatic digestion. At three time points of 7, 10, and 14 days after irradiation with 5J/cm LED red light, the expression levels of early to middle-stage osteogenic-related genes ALP, Col-1, BSP, and OPN were detected by real-time fluorescence quantitative PCR(qRT-PCR) in both control and osteogenesis experimental groups. The addition of BIX02189 could block the ERK5 signaling pathway. Under irradiation with 5J/cm LED red light, the expression levels of the ERK5 gene, related proteins ERK5, p-ERK5, as well as early to middle-stage osteogenic-related genes ALP, Col-1, BSP, and OPN were detected by qRT-PCR and Western blot in the osteogenic medium group and the osteogenic medium + BIX02189 group. RESULTS: Both low-energy LED red light and osteogenic medium could induce osteogenesis and differentiation of PDLSCs, upregulating the expression of ALP, Col-1, BSP, and OPN genes in PDLSCs. Their combination also produced a synergistic effect. Moreover, the ERK5 signaling pathway participated in the promoting effect of LED red light on the early to middle-stage osteogenic differentiation of PDLSCs, indicating a positive role of LED red light in this process. CONCLUSIONS: The ERK5 signaling pathway can mediate the promotion of early to middle-stage osteogenic differentiation of PDLSCs by low-energy LED red light.
本研究的目的是探讨低能量LED红光如何通过ERK5信号通路影响牙周膜干细胞(PDLSCs)成骨分化的早期至中期。方法:采用酶消化法从牙周膜组织中提取PDLSCs。在5J/cm LED红光照射后的第7、10和14天三个时间点,通过实时荧光定量PCR(qRT-PCR)检测对照组和成骨实验组中早期至中期成骨相关基因ALP、Col-1、BSP和OPN的表达水平。添加BIX02189可阻断ERK5信号通路。在5J/cm LED红光照射下,通过qRT-PCR和蛋白质免疫印迹法检测成骨培养基组和成骨培养基+BIX02189组中ERK5基因、相关蛋白ERK5、p-ERK5以及早期至中期成骨相关基因ALP、Col-1、BSP和OPN的表达水平。结果:低能量LED红光和成骨培养基均可诱导PDLSCs的成骨分化,上调PDLSCs中ALP、Col-1、BSP和OPN基因的表达。它们的联合使用还产生了协同效应。此外,ERK5信号通路参与了LED红光对PDLSCs早期至中期成骨分化的促进作用,表明LED红光在此过程中发挥了积极作用。结论:ERK5信号通路可介导低能量LED红光促进PDLSCs早期至中期的成骨分化。