Khalkhal Ensieh, Nobakht Fatemeh, Haidari Mohammad Hossain, Razaghi Zahra, Ghasemzad Mahsa, Sheikhan Melika, Rostami Nejad Mohammad
Proteomics Research Center, Faculty of Paramedical Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Chemical Injuries Research Center, Systems Biology and Poisoning Institute, Baqiyatallah University of Medical Sciences, Tehran, Iran.
Gastroenterol Hepatol Bed Bench. 2020 Winter;13(Suppl1):S60-S67.
this study was conducted to investigate expression of the genes associated with CD in the target tissue in order to estimate contribution of each single gene to development of immune response. Then, the same set of genes was evaluated in peripheral blood mononuclear cells (PBMCs).
Celiac disease (CD) is a chronic systemic autoimmune disease of the small intestine occurring in genetically-susceptible individuals. There are several genes related to immune response.
For this purpose, the genes related to CD were extracted from public databases (documents of proteomics and microarray-based techniques) and were organized in a protein-protein interaction network using the search tool for retrieval of interacting genes/proteins (STRING) database as a plugin of Cytoscape software version 3.6.0. The main genes were introduced and enriched via ClueGO to find the related biochemical pathways. The network was analyzed, and the most important genes were introduced based on central indices.
Among 20 CD genes as hub and bottleneck nodes, there were 7 genes with common expression in blood and intestinal tissue (C-X-C motif chemokine 11(CXCL11), granzyme B (GZMB), interleukin 15(IL-15), interleukin 17(IL-17A), interleukin 23(IL-23A), t-box transcription factor 21(TBX21), and tumor necrosis factor alpha-induced protein 3(TNFAIP3)).
The enriched biological process related to the central nodes of celiac network indicated that most of hub-bottleneck genes are the well-known ones involved in different types of autoimmune and inflammatory diseases.
本研究旨在调查与乳糜泻相关的基因在靶组织中的表达情况,以评估每个单个基因对免疫反应发展的贡献。然后,对同一组基因在外周血单个核细胞(PBMC)中进行评估。
乳糜泻(CD)是一种发生在遗传易感个体中的小肠慢性全身性自身免疫性疾病。有几个与免疫反应相关的基因。
为此,从公共数据库(蛋白质组学和基于微阵列技术的文献)中提取与乳糜泻相关的基因,并使用检索相互作用基因/蛋白质的搜索工具(STRING)数据库作为Cytoscape软件3.6.0版本的插件,将其组织成一个蛋白质-蛋白质相互作用网络。通过ClueGO引入并富集主要基因,以找到相关的生化途径。对该网络进行分析,并根据中心指标引入最重要的基因。
在作为枢纽和瓶颈节点的20个乳糜泻基因中,有7个基因在血液和肠道组织中共同表达(C-X-C基序趋化因子11(CXCL11)、颗粒酶B(GZMB)、白细胞介素15(IL-15)、白细胞介素17(IL-17A)、白细胞介素23(IL-23A)、T-box转录因子21(TBX21)和肿瘤坏死因子α诱导蛋白3(TNFAIP3))。
与乳糜泻网络中心节点相关的富集生物学过程表明,大多数枢纽-瓶颈基因是参与不同类型自身免疫和炎症性疾病的知名基因。