Karimi Mohammad Reza, Abdollahi Shahrzad, Etemadi Ardavan, Hakimiha Neda
Department of Periodontics, Faculty of Dentistry, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran.
Laser Application in Medical Sciences Research Center, Shahid Beheshti university of Medical Sciences, Tehran, Iran.
J Lasers Med Sci. 2024 Nov 3;15:e53. doi: 10.34172/jlms.2024.53. eCollection 2024.
Photobiomodulation (PBM) is considered a promising adjunctive approach in regenerative medicine. This study aimed to investigate the proliferation and adhesion of human gingival fibroblast (HGF) cells to a collagen membrane following PBM. Cultured HGF cells on a collagen membrane received PBM at wavelengths of 808 nm, 915 nm (2 and 4 J/cm), and 660 nm (2.1 and 4.2 J/cm) in interventional groups, while non-irradiated cells served as the control. On days 1 and 3 post-irradiation, cell proliferation was measured by MTT assay, and adhesion to the membrane was assessed under the scanning electron microscope (SEM). Cell proliferation significantly increased in interventional groups compared to the control, with the most significant increase at 915 nm (4 J/cm) in both time points. On the first day, the 808 nm and 660 nm lasers demonstrated similar results, significantly lower than the 915 nm laser (2 J/cm). On day 3, the 660 nm, 808 nm, and 915 nm (2 J/cm) groups showed comparable results. Qualitative analysis by the SEM identified spindle-shaped cells with multiple extended projections in 915 nm groups, especially at an energy density of 4 J/cm. Groups of 660 nm and 808 nm (4 J/cm) showed spindle-shaped cell morphology. No distinct cellular morphology indicative of enhanced adhesion was observed at 808 nm (2 J/cm). The most effective PBM setup for promoting HGF proliferation and adhesion to a collagen membrane was identified at 915 nm (4 J/cm).
光生物调节作用(PBM)被认为是再生医学中一种很有前景的辅助方法。本研究旨在调查光生物调节作用后人类牙龈成纤维细胞(HGF)在胶原膜上的增殖和黏附情况。在胶原膜上培养的HGF细胞,干预组分别接受波长为808nm、915nm(2和4J/cm)以及660nm(2.1和4.2J/cm)的光生物调节作用,未照射的细胞作为对照。在照射后第1天和第3天,通过MTT法测量细胞增殖,并在扫描电子显微镜(SEM)下评估细胞与膜的黏附情况。与对照组相比,干预组细胞增殖显著增加,在两个时间点上915nm(4J/cm)时增加最为显著。在第1天,808nm和660nm激光显示出相似的结果,显著低于915nm激光(2J/cm)。在第3天,660nm、808nm和915nm(2J/cm)组显示出相当的结果。通过扫描电子显微镜进行的定性分析发现,915nm组出现了具有多个延伸突起的纺锤形细胞,特别是在能量密度为4J/cm时。660nm和808nm(4J/cm)组呈现纺锤形细胞形态。在808nm(2J/cm)时未观察到明显表明黏附增强的细胞形态。促进HGF在胶原膜上增殖和黏附的最有效光生物调节作用设置为915nm(4J/cm)。