Department of Orthodontics and Craniofacial Development Biology, Graduate School of Biomedical & Health Sciences, Hiroshima University, Hiroshima, Japan.
Department of Oral and Maxillofacial Pathobiology, Graduate School of Biomedical & Health Sciences, Hiroshima University, Hiroshima, Japan.
Lasers Med Sci. 2024 Jul 6;39(1):174. doi: 10.1007/s10103-024-04127-7.
PURPOSE: Laser irradiation activates a range of cellular processes in the periodontal components and promotes tissue repair. However, its effect on osteogenic differentiation of human cementoblast lineage cells remains unclear. This study aimed to examine the effects of high-frequency semiconductor laser irradiation on the osteogenic differentiation of human cementoblast lineage (HCEM) cells. METHODS: HCEM cells were cultured to reach 80% confluence and irradiated with a gallium-aluminum-arsenide (Ga-Al-As) semiconductor laser with a pulse width of 200 ns and wavelength of 910 at a dose of 0-2.0 J/cm. The outcomes were assessed by analyzing the mRNA levels of alkaline phosphatase (ALP), runt-related transcription factor 2 (RUNX2), and type I collagen (COLL1) using real-time polymerase chain reaction (PCR) analysis 24 h after laser irradiation. Cell mineralization was evaluated using ALP activity, calcium deposition, and Alizarin Red staining. RESULTS: The laser-irradiated HCEM cells showed significantly enhanced gene expression levels of ALP, RUNX2, and COLL1 as well as ALP activity and calcium concentration in the culture medium compared with the non-irradiated cells. In addition, enhanced calcification deposits were confirmed in the laser-irradiated group compared with the non-irradiated group at 21 and 28 days after the induction of osteogenic differentiation. CONCLUSION: High-frequency semiconductor laser irradiation enhances the osteogenic differentiation potential of cultured HCEM cells, underscoring its potential utility for periodontal tissue regeneration.
目的:激光照射激活牙周组织中的一系列细胞过程,促进组织修复。然而,其对人成牙骨质细胞系的成骨分化的影响尚不清楚。本研究旨在探讨高频半导体激光照射对人成牙骨质细胞系(HCEM)细胞成骨分化的影响。
方法:将 HCEM 细胞培养至 80%汇合,并用脉冲宽度为 200ns、波长为 910nm 的砷化镓-铝-砷(Ga-Al-As)半导体激光照射,剂量为 0-2.0J/cm。激光照射 24h 后,通过实时聚合酶链反应(PCR)分析碱性磷酸酶(ALP)、 runt 相关转录因子 2(RUNX2)和 I 型胶原(COLL1)的 mRNA 水平来评估结果。通过碱性磷酸酶活性、钙沉积和茜素红染色来评估细胞矿化。
结果:与未照射细胞相比,激光照射的 HCEM 细胞的 ALP、RUNX2 和 COLL1 的基因表达水平以及培养基中的 ALP 活性和钙浓度均显著增强。此外,在诱导成骨分化后 21 天和 28 天,与未照射组相比,激光照射组的钙化沉积物明显增多。
结论:高频半导体激光照射增强了培养的 HCEM 细胞的成骨分化潜能,这突显了其在牙周组织再生中的潜在应用价值。
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