首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Synthetic Human β Defensin-3-C15 Peptide in Endodontics: Potential Therapeutic Agent in Streptococcus gordonii Lipoprotein-Stimulated Human Dental Pulp-Derived Cells
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Synthetic Human β Defensin-3-C15 Peptide in Endodontics: Potential Therapeutic Agent in Streptococcus gordonii Lipoprotein-Stimulated Human Dental Pulp-Derived Cells

机译:牙髓学中的合成人βDefensin-3-C15肽:戈登氏链球菌脂蛋白刺激的人牙髓衍生细胞中的潜在治疗剂

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摘要

Human β defensin-3-C15, an epithelium-derived cationic peptide that has antibacterial/antifungal and immuno-regulatory properties, is getting attention as potential therapeutic agent in endodontics. This study aimed to investigate if synthetic human β defensin-3-C15 (HBD3-C15) peptides could inhibit inflammatory responses in human dental pulp cells (hDPCs), which had been induced by gram-positive endodontic pathogen. hDPC explant cultures were stimulated with lipoprotein extracts for 24 h to induce expression of pro-inflammatory mediators. The cells were then treated with either HBD3-C15 (50 μg/mL) or calcium hydroxide (CH, 100 μg/mL) as control for seven days, to assess their anti-inflammatory effects. Quantitative RT-PCR analyses and multiplex assays showed that lipoprotein induced the inflammatory reaction in hDPCs. There was a significant reduction of IL-8 and MCP-1 within 24 h of treatment with either CH or HBD3-C15 ( < 0.05), which was sustained over 1 week of treatment. Alleviation of inflammation in both medications was related to COX-2 expression and PGE2 secretion ( < 0.05), rather than TLR2 changes ( > 0.05). These findings demonstrate comparable effects of CH and HDB3-C15 as therapeutic agents for inflamed hDPCs.
机译:人β防御素3-C15是一种具有抗菌/抗真菌和免疫调节特性的上皮衍生阳离子肽,在牙髓治疗中作为潜在的治疗剂受到关注。这项研究旨在研究合成的人β防御素-3-C15(HBD3-C15)肽是否能抑制人牙髓细胞(hDPC)的炎症反应,而该反应是由革兰氏阳性牙髓病原体引起的。用脂蛋白提取物刺激hDPC外植体培养物24小时,以诱导促炎性介质的表达。然后将细胞用HBD3-C15(50μg/ mL)或氢氧化钙(CH,100μg/ mL)作为对照处理7天,以评估其抗炎作用。定量RT-PCR分析和多重分析表明,脂蛋白诱导了hDPC中的炎症反应。 CH或HBD3-C15治疗24小时内IL-8和MCP-1明显减少(<0.05),治疗1周后持续。两种药物的炎症缓解均与COX-2表达和PGE2分泌有关(<0.05),而不是与TLR2的变化有关(> 0.05)。这些发现证明CH和HDB3-C15作为发炎的hDPC的治疗剂具有可比的效果。

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