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白细胞介素-6/信号转导子和转录激活子途径负责在唾液腺导管上皮细胞中诱导REI Iα(干燥综合征患者的一种新自身抗原)的基因表达。

Interleukin-6/STAT pathway is responsible for the induction of gene expression of REG Iα, a new auto-antigen in Sjögren׳s syndrome patients, in salivary duct epithelial cells.

作者信息

Fujimura Takanori, Fujimoto Takashi, Itaya-Hironaka Asako, Miyaoka Tomoko, Yoshimoto Kiyomi, Yamauchi Akiyo, Sakuramoto-Tsuchida Sumiyo, Kondo Saori, Takeda Maiko, Tsujinaka Hiroki, Azuma Masayuki, Tanaka Yasuhito, Takasawa Shin

机构信息

Department of Biochemistry, Nara Medical University, Kashihara 634-8521, Nara, Japan.

The Center for Rheumatic Diseases, Nara Medical University Hospital, Kashihara 634-8522, Nara, Japan.

出版信息

Biochem Biophys Rep. 2015 May 30;2:69-74. doi: 10.1016/j.bbrep.2015.05.006. eCollection 2015 Jul.

Abstract

The regenerating gene, , was originally isolated from a rat regenerating islet cDNA library, and its human homolog was named . Recently, we reported that mRNA as well as its product were overexpressed in ductal epithelial cells in the minor salivary glands of Sjögren׳s syndrome (SS) patients. This study was undertaken to elucidate the role of cytokines and the subsequent intracellular mechanism for induction of in the salivary glands of SS patients. We prepared a reporter plasmid containing promoter (-1190/+26) upstream of a luciferase reporter gene. The promoter plasmid was introduced by lipofection into human NS-SV-DC and rat A5 salivary ductal cells. The cells were treated with interleukin (IL)-6, IL-8, and a combination of the two. Thereafter transcriptional activity of was measured by luciferase assay. We found that IL-6 stimulation, but not IL-8, significantly enhanced the promoter activity in salivary ductal cells. Deletion analysis revealed that the region of -141 to -117 of the gene was responsible for the promoter activation by IL-6, which contains a consensus sequence for signal transduction and activation of transcription (STAT). The introduction of siRNA for human STAT3 abolished IL-6-induced transcription. These results showed that IL-6 stimulation induced transcription through STAT3 activation and binding to the consensus sequence of promoter in salivary ductal cells. This IL-6/STAT dependent induction might play a role in the pathogenesis of SS.

摘要

再生基因最初是从大鼠再生胰岛cDNA文库中分离出来的,其人类同源基因被命名为 。最近,我们报道了在干燥综合征(SS)患者小唾液腺的导管上皮细胞中, 信使核糖核酸及其产物均过度表达。本研究旨在阐明细胞因子的作用以及随后SS患者唾液腺中诱导 表达的细胞内机制。我们制备了一个报告质粒,该质粒在荧光素酶报告基因上游含有 启动子(-1190/+26)。通过脂质转染将启动子质粒导入人NS-SV-DC和大鼠A5唾液导管细胞。用白细胞介素(IL)-6、IL-8以及二者的组合处理这些细胞。此后,通过荧光素酶测定法测量 的转录活性。我们发现IL-6刺激而非IL-8能显著增强唾液导管细胞中的 启动子活性。缺失分析表明, 基因-141至-117区域负责IL-6对启动子的激活,该区域包含信号转导和转录激活因子(STAT)的共有序列。导入针对人STAT3的小干扰RNA可消除IL-6诱导的 转录。这些结果表明,IL-6刺激通过激活STAT3并与唾液导管细胞中 启动子的共有序列结合来诱导 转录。这种IL-6/STAT依赖性的 诱导可能在SS的发病机制中起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6b9/5668644/ba9ed3953a6b/fx1.jpg

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