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口腔扁平苔藓T细胞中自噬相关基因表达的改变与临床特征相关。

Altered Autophagy-Associated Genes Expression in T Cells of Oral Lichen Planus Correlated with Clinical Features.

作者信息

Tan Ya-Qin, Zhang Jing, Du Ge-Fei, Lu Rui, Chen Guan-Ying, Zhou Gang

机构信息

The State Key Laboratory Breeding Base of Basic Science of Stomatology (Hubei-MOST) and Key Laboratory of Oral Biomedicine Ministry of Education, School and Hospital of Stomatology, Wuhan University, Luoyu Road 237, Wuhan 430079, China.

The State Key Laboratory Breeding Base of Basic Science of Stomatology (Hubei-MOST) and Key Laboratory of Oral Biomedicine Ministry of Education, School and Hospital of Stomatology, Wuhan University, Luoyu Road 237, Wuhan 430079, China; Department of Oral Medicine, School and Hospital of Stomatology, Wuhan University, Luoyu Road 237, Wuhan 430079, China.

出版信息

Mediators Inflamm. 2016;2016:4867368. doi: 10.1155/2016/4867368. Epub 2016 Feb 15.

Abstract

Oral lichen planus (OLP) is a T cell-mediated inflammatory autoimmune disease. Autophagy has emerged as a fundamental trafficking event in mediating T cell response, which plays crucial roles in innate and adaptive immunity. The present study mainly investigated the mRNA expression of autophagy-associated genes in peripheral blood T cells of OLP patients and evaluated correlations between their expression and the clinical features of OLP. Five differentially expressed autophagy-associated genes were identified by autophagy array. Quantitative real-time RT-PCR results confirmed that IGF1 expression in the peripheral blood T cells of OLP patients was significantly higher than that in controls, especially in female and middle-aged (30-50 years old) OLP patients. In addition, ATG9B mRNA levels were significantly lower in nonerosive OLP patients. However, no significant differences were found in the expression of HGS, ESR1, and SNCA between OLP patients and controls. Taken together, dysregulation of T cell autophagy may be involved in immune response of OLP and may be correlated with clinical patterns.

摘要

口腔扁平苔藓(OLP)是一种T细胞介导的炎症性自身免疫性疾病。自噬已成为介导T细胞反应的一种基本转运事件,在固有免疫和适应性免疫中起关键作用。本研究主要调查了OLP患者外周血T细胞中自噬相关基因的mRNA表达,并评估了其表达与OLP临床特征之间的相关性。通过自噬芯片鉴定出五个差异表达的自噬相关基因。定量实时RT-PCR结果证实,OLP患者外周血T细胞中IGF1的表达显著高于对照组,尤其是女性和中年(30 - 50岁)OLP患者。此外,非糜烂性OLP患者的ATG9B mRNA水平显著降低。然而,OLP患者与对照组之间HGS、ESR1和SNCA的表达未发现显著差异。综上所述,T细胞自噬失调可能参与OLP的免疫反应,并可能与临床类型相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3d1/4770128/f5489dab0f14/MI2016-4867368.001.jpg

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