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808纳米光生物调节疗法后人牙髓干细胞的线粒体氧消耗及免疫细胞化学:一项三维细胞培养研究

Mitochondrial Oxygen Consumption and Immunocytochemistry of Human Dental Pulp Stem Cell Following 808 nm PBM Therapy: A 3D Cell Culture Study.

作者信息

Sleep Simone L, Ranjit Eliza, Gunter Jennifer, Hryciw Deanne H, Arany Praveen, George Roy

机构信息

School of Medicine and Dentistry, Griffith University, Southport, Australia.

Australian Prostate Cancer Research Centre, QLD, Centre for Genomics and Personalised Health, School of Biomedical Science, Queensland University of Technology, Translational Research Institute, Brisbane, Australia.

出版信息

J Biophotonics. 2025 Apr 28:e70051. doi: 10.1002/jbio.70051.

Abstract

This study investigated the impact of 808 nm laser photobiomodulation (PBM) on mitochondrial respiration and osteogenic protein expression (OCN, OPN, ALP, RUNX2, COL-1, BMP-2) in human dental pulp stem cells (hDPSCs) within a 3D hydrogel model. hDPSCs were isolated from third molars and maintained under hypoxic conditions. Cells received PBM at 5 and 15 J/cm using an 808 nm diode laser. The study showed that 808 nm PBM can alter mitochondrial respiration, with 5 J/cm enhancing osteogenic protein expression (OCN, ALP, OPN, RUNX2) but failing to sustain BMP-2 at 24 h. In contrast, 15 J/cm induced stronger upregulation and prolonged BMP-2 expression, suggesting an optimal dose for sustained osteogenic activity. BMP-2 was later downregulated, and COL-1 remained unchanged post-PBM. Importantly, this study indicates the dose-specific PBM modulation of mitochondrial respiration and protein expression, but further research is required to optimize treatment protocols.

摘要

本研究在三维水凝胶模型中,探究了808纳米激光光生物调节(PBM)对人牙髓干细胞(hDPSCs)线粒体呼吸和成骨蛋白表达(骨钙素、骨桥蛋白、碱性磷酸酶、RUNX2、I型胶原蛋白、骨形态发生蛋白-2)的影响。从第三磨牙中分离出hDPSCs,并在低氧条件下培养。使用808纳米二极管激光,以5和15焦每平方厘米的剂量对细胞进行PBM照射。研究表明,808纳米PBM可改变线粒体呼吸,5焦每平方厘米可增强成骨蛋白表达(骨钙素、碱性磷酸酶、骨桥蛋白、RUNX2),但在24小时时无法维持骨形态发生蛋白-2的表达。相比之下,15焦每平方厘米诱导更强的上调并延长了骨形态发生蛋白-2的表达,表明这是持续成骨活性的最佳剂量。骨形态发生蛋白-2随后下调,I型胶原蛋白在PBM后保持不变。重要的是,本研究表明了PBM对线粒体呼吸和蛋白表达的剂量特异性调节,但需要进一步研究以优化治疗方案。

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