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Effects of hydrogen sulfide on the expression of alkaline phosphatase, osteocalcin and collagen type I in human periodontal ligament cells induced by tension force stimulation

机译:硫化氢对张力刺激诱导的人牙周膜细胞碱性磷酸酶,骨钙素和Ⅰ型胶原蛋白表达的影响

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Periodontal ligament cells (PDLCs) are important in homeostasis and remodeling in the mechanically-stimulated periodontium. The aim of the present study was to investigate the effects of hydrogen sulfide (H2S) on periodontal tissue remodeling by examining the mRNA and protein expression levels of alkaline phosphatase (ALP), osteocalcin (OCN) and collagen type I (COL-1) in human (h)PDLCs induced by tension force application. Cultured hPDLCs were treated with H2S for 24 h, followed by application of a tension force for 1, 3 and 6 h. Cell proliferation and apoptosis were determined using a Cell Counting Kit 8 assay and flow cytometric analysis, respectively. The mRNA expression levels of ALP, OCN and COL-1 were quantified using reverse transcription-quantitative polymerase chain reaction analysis, and western blot analysis was used to detect the protein levels of ALP, OCN and COL-1. The results demonstrated that the mRNA and protein expression levels of ALP, OCN and COL-1 increased with H2S treatment in a concentration-dependent manner, which was enhanced by the application of tension force in a relatively short period of time. These findings suggested that H2S may be important in periodontal tissue remodeling during orthodontic tooth movement via increasing hPDLC differentiation, tissue mineralization, bone formation and collagen synthesis.
机译:牙周膜细胞(PDLC)在机械刺激的牙周膜的稳态和重塑中很重要。本研究的目的是通过检查碱性磷酸酶(ALP),骨钙素(OCN)和I型胶原(COL-1)的mRNA和蛋白质表达水平来研究硫化氢(H2S)对牙周组织重塑的影响。通过施加张力诱导的人(h)PDLC。将培养的hPDLC用H2S处理24小时,然后施加拉力1、3和6小时。分别使用Cell Counting Kit 8分析法和流式细胞仪分析确定细胞增殖和凋亡。使用逆转录定量聚合酶链反应分析定量ALP,OCN和COL-1的mRNA表达水平,并使用western blot分析检测ALP,OCN和COL-1的蛋白水平。结果表明,H2S处理后,ALP,OCN和COL-1的mRNA和蛋白表达水平呈浓度依赖性增加,而在相对较短的时间内施加张力会增强这种表达。这些发现表明,H2S可能通过增加hPDLC分化,组织矿化,骨形成和胶原蛋白合成,在正畸牙齿移动过程中对牙周组织重塑起重要作用。

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