首页> 外文期刊>Journal of Indian Society of Periodontology >Evaluation of mRNA expression of the transcription factors of Th1 and Th2 subsets (T-bet and GATA-3) in periodontal health and disease - A pilot study in south Indian population
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Evaluation of mRNA expression of the transcription factors of Th1 and Th2 subsets (T-bet and GATA-3) in periodontal health and disease - A pilot study in south Indian population

机译:牙周健康和疾病中Th1和Th2子集转录因子(T-bet和GATA-3)mRNA表达的评估-印度南部人群的一项初步研究

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Background: Based on their respective pro- or anti-inflammatory cytokine profiles, the Th1/Th2 paradigm explains pathogenic mechanisms involved in periodontal disease. Establishment of Th1 and Th2 subsets from a naive T-cell precursor depends on transcriptional regulation. The aim of this study was to compare the expression of master transcription factor regulators T-bet and GATA-3, respectively, to indicate the predominance of Th1 and Th2 subsets in the presence and absence of periodontal disease. Materials and Methods: A gingival tissue biopsy sample was obtained from each of 10 severe periodontitis patients (>5 mm attachment loss) and 10 periodontally healthy patients (no attachment loss). Biopsies were immediately processed by real-time reverse transcriptase polymerase chain reaction and the difference in mRNA expression of T-bet and GATA-3 was assessed for each group. Results: The mRNA expression of T-bet was marginally increased about 1.31-fold in disease, while the GATA-3 levels showed a significant decrease of 4.39-fold in disease. Conclusion: The advanced periodontal lesions lack Th2 cells, which produce anti-inflammatory cytokines. The biopsies were therefore dominated by Th1 cells, which activate macrophages and osteoclasts.
机译:背景:Th1 / Th2范式基于它们各自的促炎或抗炎细胞因子谱,解释了牙周疾病的致病机制。从幼稚的T细胞前体中建立Th1和Th2子集取决于转录调控。这项研究的目的是比较主转录因子调节剂T-bet和GATA-3的表达,以表明在有牙周病和无牙周病的情况下Th1和Th2亚型占优势。材料和方法:从10位重度牙周炎患者(> 5 mm附着力丧失)和10位牙周健康患者(无附着力丧失)中分别获取牙龈组织活检样品。立即通过实时逆转录酶聚合酶链反应处理活检,并评估每组T-bet和GATA-3 mRNA表达的差异。结果:疾病中T-bet的mRNA表达略有增加约1.31倍,而疾病中GATA-3水平显着下降了4.39倍。结论:晚期牙周病变缺乏Th2细胞,产生抗炎细胞因子。因此,活检是由Th1细胞控制的,Th1细胞激活了巨噬细胞和破骨细胞。

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