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Leptin receptor is up-regulated in inflamed human dental pulp

机译:瘦人受体在发炎的人类牙髓中上调

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Introduction After leptin receptor (LEPR) identification in hematopoietic, immune system, and other tissues, a role for leptin regulating inflammation and immune response has been accepted. This study aims to describe the possible expression of LEPR in healthy human dental pulp and to compare it with LEPR expression in inflamed human dental pulp. Methods Twenty-one pulp samples were obtained from freshly extracted caries-free and restoration-free human third molars. In 7 third molars (inflamed pulp group), inflammation was experimentally induced before extraction. Pulp samples were processed, and LEPR expression was determined by quantitative real-time polymerase chain reaction, and the amount of LEPR protein was analyzed by immunoblot. Results All healthy and inflamed dental pulp samples expressed LEPR. Western blot analysis of human dental pulp revealed the presence of a protein with an apparent molecular weight of approximately 120 kDa, which corresponds to the estimated molecular weight of LEPR. The expression of LEPR mRNA was confirmed by quantitative real-time polymerase chain reaction analysis, and the size of the amplified fragment (338 base pairs for LEPR and 194 base pairs for cyclophilin) was assessed by agarose gel electrophoresis. The relative amount of LEPR in inflamed pulps was approximately 50% higher than in healthy pulps (P <.05). Conclusions The presence of LEPR in human dental pulp tissues has been demonstrated for the first time. The up-regulation of LEPR expression in inflamed pulp samples suggests that leptin can play a role in inflammatory and local immune responses in human dental pulp.
机译:简介在瘦素受体(LEPR)在造血,免疫系统和其他组织中鉴定后,瘦素调节炎症和免疫反应的作用已被接受。这项研究旨在描述在健康的人类牙髓中LEPR的可能表达,并将其与发炎的人类牙髓中的LEPR表达进行比较。方法从新鲜提取的无龋和无修复的人类第三磨牙中提取二十一个牙髓样品。在7个第三磨牙(发炎的牙髓组)中,在提取前实验性地诱发了炎症。处理纸浆样品,并通过定量实时聚合酶链反应确定LEPR表达,并通过免疫印迹分析LEPR蛋白的量。结果所有健康和发炎的牙髓样品均表达LEPR。对人牙髓的蛋白质印迹分析表明,存在表观分子量约为120 kDa的蛋白质,该蛋白质与LEPR的估计分子量相对应。通过实时定量聚合酶链反应分析确认了LEPR mRNA的表达,并通过琼脂糖凝胶电泳评估了扩增片段的大小(LEPR为338个碱基对,亲环蛋白为194个碱基对)。发炎果肉中LEPR的相对量比健康果肉中高约50%(P <.05)。结论首次证明了人牙髓组织中存在LEPR。炎症牙髓样品中LEPR表达的上调提示瘦蛋白可以在人类牙髓的炎症和局部免疫反应中发挥作用。

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