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Low-power laser irradiation promotes the proliferation and osteogenic differentiation of human periodontal ligament cells via cyclic adenosine monophosphate

机译:低功率激光照射通过环状磷酸腺苷促进人牙周膜细胞的增殖和成骨分化

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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 (660nm) daily with doses of 0, 1, 2 or 4J?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 2J?cm?2 significantly promoted hPDL cell proliferation at days 3 and 5. In addition, LPLI at energy doses of 2 and 4J?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.
机译:保持或改善牙周膜(PDL)功能对于恢复牙周缺损至关重要。这项研究的目的是评估低功率激光照射(LPLI)对人PDL(hPDL)细胞增殖和成骨分化的生理影响。每天用0、1、2或4J?cm?2的剂量辐照培养的hPDL细胞(660nm)。细胞增殖通过3- [4,5-二甲基噻唑-2-基] -2,5-二苯基四氮唑溴化物(MTT)分析进行评估,LPLI对茜素红S染色和碱性磷酸酶的诱导对成骨分化的影响( ALP)活动。此外,通过实时逆转录-聚合酶链反应(RT-PCR)确认了成骨标记基因的表达。我们的数据表明,剂量为2J?cm?2的LPLI在第3天和第5天显着促进了hPDL细胞的增殖。此外,能量剂量为2J和4J?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,环磷酸一腺苷(cAMP)是LPLI介导的对hPDL细胞作用的关键调节剂。这项研究表明,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的潜在用途。

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