Institute of Biomedical Engineering, National Cheng Kung University, Tainan, Taiwan.
Int J Oral Sci. 2013 Jun;5(2):85-91. doi: 10.1038/ijos.2013.38. Epub 2013 Jun 21.
Retaining or improving periodontal ligament (PDL) function is crucial for restoring periodontal defects. The aim of this study was to evaluate the physiological effects of low-power laser irradiation (LPLI) on the proliferation and osteogenic differentiation of human PDL (hPDL) cells. Cultured hPDL cells were irradiated (660 nm) daily with doses of 0, 1, 2 or 4 J⋅cm(-2). Cell proliferation was evaluated by the 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide (MTT) assay, and the effect of LPLI on osteogenic differentiation was assessed by Alizarin Red S staining and alkaline phosphatase (ALP) activity. Additionally, osteogenic marker gene expression was confirmed by real-time reverse transcription-polymerase chain reaction (RT-PCR). Our data showed that LPLI at a dose of 2 J⋅cm(-2) significantly promoted hPDL cell proliferation at days 3 and 5. In addition, LPLI at energy doses of 2 and 4 J⋅cm(-2) showed potential osteogenic capacity, as it stimulated ALP activity, calcium deposition, and osteogenic gene expression. We also showed that cyclic adenosine monophosphate (cAMP) is a critical regulator of the LPLI-mediated effects on hPDL cells. This study shows that LPLI can promote the proliferation and osteogenic differentiation of hPDL cells. These results suggest the potential use of LPLI in clinical applications for periodontal tissue regeneration.
保留或改善牙周韧带(PDL)功能对于牙周缺损的修复至关重要。本研究旨在评估低功率激光照射(LPLI)对人牙周韧带(hPDL)细胞增殖和成骨分化的生理影响。培养的 hPDL 细胞每天用 0、1、2 或 4 J ⋅ cm(-2) 的剂量进行照射(660nm)。通过 3-[4,5-二甲基噻唑-2-基]-2,5-二苯基四氮唑溴盐(MTT)测定评估细胞增殖,通过茜素红 S 染色和碱性磷酸酶(ALP)活性评估 LPLI 对成骨分化的影响。此外,通过实时逆转录-聚合酶链反应(RT-PCR)证实成骨标记基因的表达。我们的数据显示,2 J ⋅ cm(-2) 的 LPLI 显著促进了 hPDL 细胞在第 3 天和第 5 天的增殖。此外,2 J ⋅ cm(-2) 和 4 J ⋅ cm(-2) 的 LPLI 显示出潜在的成骨能力,因为它刺激了 ALP 活性、钙沉积和成骨基因表达。我们还表明,环磷酸腺苷(cAMP)是 LPLI 对 hPDL 细胞影响的关键调节剂。本研究表明,LPLI 可以促进 hPDL 细胞的增殖和成骨分化。这些结果表明 LPLI 在牙周组织再生的临床应用中具有潜力。