首页|炎症性肠病合并皮肤损害患者外泌体差异表达蛋白质及发病机制研究

炎症性肠病合并皮肤损害患者外泌体差异表达蛋白质及发病机制研究

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目的 探讨炎症性肠病(IBD)合并皮肤损害患者外泌体差异表达蛋白质及发病机制.方法 选取杭州市第三人民医院2020年1月至2021年12月收治的5例IBD以及5例IBD合并皮肤损害患者为研究对象,分别为IBD组、IBD+皮肤损害组;另选取本院同期体检的5名年龄和性别匹配的健康志愿者为对照组.提取3组对象血清外泌体,检测差异表达蛋白质;采用基因本论(GO)和京都基因和基因组数据库(KEGG)对差异表达蛋白质进行生物信息学分析.结果 共鉴定829种蛋白质,其中包含定量信息的蛋白质726种.与对照组比较,IBD组有15种蛋白质表达上调,21种蛋白质表达下调;IBD+皮肤损害组有24种蛋白质表达上调,25种蛋白质表达下调;与IBD组比较,IBD+皮肤损害组有12种蛋白质表达上调和8种蛋白质表达下调.GO分析显示,IBD组与对照组、IBD+皮肤损害组与对照组、IBD+皮肤损害组与IBD组差异表达蛋白质涉及的生物过程包括刺激反应、细胞过程、单有机过程、生物调节等,细胞组成主要包括细胞、细胞膜外域、细胞器等,分子功能主要包括结合、催化活性等.KEGG分析显示,旧D组与对照组差异表达蛋白质主要与细胞黏附、离子跨膜运输调控、细胞形态分化等有关;旧D+皮肤损害组与对照组差异表达蛋白质主要与细胞分泌、细胞分解代谢、分泌调节有关;IBD+皮肤损害组与IBD组差异表达蛋白质主要与细胞胺代谢、NIK/NF-κB信号通路、细胞周期过程的负调控等有关.结论 本研究基于TMT蛋白质组学分析筛选出IBD+皮肤损害患者血清外泌体差异表达蛋白质,这些蛋白质参与IBD合并皮肤损害的代谢相关通路及病变的发生.
Differential expression of exosome protein and its pathogenesis in patients with inflammatory bowel disease complicated with skin lesions
Objective To investigate the differential expression of exosome protein and its pathogenesis in patients with inflammatory bowel disease(IBD)complicated with skin lesions.Methods Five patients with IBD and another five patients with IBD combined with skin damage admitted to Hangzhou Third People's Hospital from January 2020 to December 2021 were selected as the study objects as respectively the IBD group and IBD+skin damage group.In addition,five age-and sex-matched healthy volunteers were selected as the control group.Serum exosomes were extracted from patients in the 3 groups and their differentially expressed proteins were identified.Bioinformatic analysis of differentially expressed proteins was performed using gene ontology(GO)and Kyoto encyclopedia of genes and genomes(KEGG).Results According to proteomic results,a total of 829 proteins were identified,including 726 proteins with quantitative information.Compared with the control group,15 proteins were up-regulated and 21 proteins were down-regulated in IBD group,while in IBD+skin damage group,24 proteins were up-regulated and 25 proteins were down-regulated.Compared with IBD group,12 proteins were up-regulated and 8 proteins were down-regulated in IBD+skin damage group.GO analysis showed that the biological processes involved in the differential expression of proteins between the IBD group and the control group,between the IBD+skin damage group and the control group,and between the IBD+skin damage group and the IBD group included stimulation response,cellular processes,single organic processes,biological regulation,etc.The cell composition mainly included cells,outer membrane domain,organelles,etc.The molecular functions mainly included binding and catalytic activity.KEGG analysis showed that the difference of protein expression between IBD group and control group was mainly related to cell adhesion,ion transmembrane transport and cell morphological differentiation.The difference of expression of protein between IBD+skin damage group and control group was mainly related to cell secretion,cell catabolism and secretion regulation.The difference of protein expression between IBD+skin damage group and IBD group was mainly related to negative regulation of cellular amine metabolism,NIK/NF-κB signaling pathway,and cell cycle processes.Conclusion In this study,based on TMT proteomic analysis,differential expression proteins of serum exosomes in patients with IBD+skin damage are screened,and these proteins are involved in metabolic pathways and biological functions associated with IBD and skin damage.

Inflammatory bowel diseaseSkin diseasesExosomesDifferentially expressed proteinSignaling pathway

吴俊俊、李珍、李华铭、李春霞、朱伟琴、王宇芳

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310000 杭州市第三人民医院消化内科

炎症性肠病 皮肤损害 外泌体 差异表达蛋白质 信号通路

浙江省医药卫生科技计划项目

2019KY505

2024

浙江医学
浙江省医学会

浙江医学

CSTPCD
影响因子:0.428
ISSN:1006-2785
年,卷(期):2024.46(1)
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