首页> 外文期刊>国际口腔科学杂志(英文版) >Low-power laser irradiation promotes the proliferation and osteogenic differentiation of human periodontal ligament cells via cyclic adenosine monophosphate
【24h】

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单磷酸环状腺苷促进人牙周膜细胞的增殖和成骨分化

获取原文
获取原文并翻译 | 示例
           

摘要

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?cm22. 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?cm22 significantly promoted hPDL cell proliferation at days 3 and 5. In addition, LPLI at energy doses of 2 and 4 J?cm22 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4 J?cm22的剂量辐照培养的hPDL细胞(660 nm)。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。我们的数据显示,在第3天和第5天,剂量为2 J?cm22的LPLI显着促进hPDL细胞增殖。此外,在能量剂量为2和4 J?cm22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。

著录项

  • 来源
    《国际口腔科学杂志(英文版)》 |2013年第2期|85-91|共7页
  • 作者单位

    Institute of Biomedical Engineering, National Cheng Kung University, Tainan, Taiwan;

    Department of Physical Medicine and Rehabilitation, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan;

    Department of oral Hygiene, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan;

    Institute of Biomedical Engineering, National Cheng Kung University, Tainan, Taiwan;

    School of Dentistry, College of Dental Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan;

    School of Dentistry, College of Dental Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan;

  • 收录信息 中国科学引文数据库(CSCD);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号