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功能性 Toll 样受体-9 启动子多态性(-1237T/C)在终末期肾病风险增加中的作用:一项病例对照研究。

Role of the functional Toll-Like receptor-9 promoter polymorphism (-1237T/C) in increased risk of end-stage renal disease: a case-control study.

机构信息

School of Public Health, National Defense Medical Center, Taipei, Taiwan, Republic of China.

出版信息

PLoS One. 2013;8(3):e58444. doi: 10.1371/journal.pone.0058444. Epub 2013 Mar 5.

Abstract

Inflammation induced by infectious and noninfectious triggers in the kidney may lead to end stage renal disease (ESRD). Toll-like receptor 9 (TLR-9) a receptor for CpG DNA is involved in activation of immune cells in renal disease and may contribute to chronic inflammatory disease progression through an interleukin-6 (IL-6) dependent pathway. Previous studies indicate that -1237T/C confers regulatory effects on TLR-9 transcription. To date the effect of TLR-9 polymorphisms on ESRD remains unknown. We performed a case-control study and genotyped 630 ESRD patients and 415 controls for -1237T/C, -1486T/C and 1635G/A by real-time PCR assays and assessed plasma concentration of IL-6 by ELISA. Haplotype association analysis was performed using the Haploview package. A luciferase reporter assay and real-time PCR were used to test the function of the -1237T/C promoter polymorphism. A significant association between -1237T/C in TLR-9 and ESRD was identified. The TCA, TTA and CCA haplotype of TLR-9 were associated with ESRD. ESRD patients carrying -1237TC had a higher mean plasma IL-6 level when compared with -1237TT. The TLR-9 transcriptional activity of the variant -1237CC allele is higher than the -1237TT allele. The results indicate that in a Han Chinese population the presence of the C allele of -1237T/C in the TLR-9 gene increases susceptibility towards development of ESRD. In vitro studies demonstrate that -1237T/C may be involved in the development of ESRD through transcriptional modulation of TLR-9.

摘要

在肾脏中,由传染性和非传染性触发因素引起的炎症可能导致终末期肾病 (ESRD)。Toll 样受体 9 (TLR-9) 是一种 CpG DNA 的受体,它参与了肾脏疾病中免疫细胞的激活,并且可能通过白细胞介素-6 (IL-6) 依赖性途径促进慢性炎症疾病的进展。以前的研究表明,-1237T/C 对 TLR-9 转录具有调节作用。迄今为止,TLR-9 多态性对 ESRD 的影响尚不清楚。我们进行了一项病例对照研究,通过实时 PCR 检测和 ELISA 评估 IL-6 的血浆浓度,对 630 名 ESRD 患者和 415 名对照者进行了-1237T/C、-1486T/C 和 1635G/A 的基因分型。使用 Haploview 包进行单体型关联分析。使用荧光素酶报告基因检测和实时 PCR 检测了-1237T/C 启动子多态性的功能。TLR-9 中的-1237T/C 与 ESRD 之间存在显著关联。TLR-9 的 TCA、TTA 和 CCA 单体型与 ESRD 相关。与-1237TT 相比,携带-1237TC 的 ESRD 患者的平均血浆 IL-6 水平更高。变异体-1237CC 等位基因的 TLR-9 转录活性高于-1237TT 等位基因。结果表明,在汉族人群中,TLR-9 基因中的 C 等位基因-1237T/C 的存在增加了发展为 ESRD 的易感性。体外研究表明,-1237T/C 可能通过 TLR-9 的转录调节参与 ESRD 的发生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd7e/3589433/0c93498eb673/pone.0058444.g001.jpg

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