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对比分析炎症和非炎症结肠活检组织,揭示溃疡性结肠炎患者存在强烈的蛋白质组学炎症特征。

Comparative analysis of inflamed and non-inflamed colon biopsies reveals strong proteomic inflammation profile in patients with ulcerative colitis.

机构信息

Department of Food Science, Aarhus University, Tjele 8830, Denmark.

出版信息

BMC Gastroenterol. 2012 Jun 24;12:76. doi: 10.1186/1471-230X-12-76.

DOI:10.1186/1471-230X-12-76
PMID:22726388
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3441502/
Abstract

BACKGROUND

Accurate diagnostic and monitoring tools for ulcerative colitis (UC) are missing. Our aim was to describe the proteomic profile of UC and search for markers associated with disease exacerbation. Therefore, we aimed to characterize specific proteins associated with inflamed colon mucosa from patients with acute UC using mass spectrometry-based proteomic analysis.

METHODS

Biopsies were sampled from rectum, sigmoid colon and left colonic flexure from twenty patients with active proctosigmoiditis and from four healthy controls for proteomics and histology. Proteomic profiles of whole colonic biopsies were characterized using 2D-gel electrophoresis, and peptide mass fingerprinting using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) was applied for identification of differently expressed protein spots.

RESULTS

A total of 597 spots were annotated by image analysis and 222 of these had a statistically different protein level between inflamed and non-inflamed tissue in the patient group. Principal component analysis clearly grouped non-inflamed samples separately from the inflamed samples indicating that the proteomic signature of colon mucosa with acute UC is strong. Totally, 43 individual protein spots were identified, including proteins involved in energy metabolism (triosephosphate isomerase, glycerol-3-phosphate-dehydrogenase, alpha enolase and L-lactate dehydrogenase B-chain) and in oxidative stress (superoxide dismutase, thioredoxins and selenium binding protein).

CONCLUSIONS

A distinct proteomic profile of inflamed tissue in UC patients was found. Specific proteins involved in energy metabolism and oxidative stress were identified as potential candidate markers for UC.

摘要

背景

溃疡性结肠炎(UC)缺乏准确的诊断和监测工具。我们的目的是描述 UC 的蛋白质组特征,并寻找与疾病恶化相关的标志物。因此,我们旨在使用基于质谱的蛋白质组分析来描述来自急性 UC 患者的炎症结肠黏膜相关的特定蛋白质。

方法

从二十名患有活动期直肠乙状结肠炎和四名健康对照者的直肠、乙状结肠和左结肠弯曲处采集活检组织,用于蛋白质组学和组织学研究。使用 2D 凝胶电泳对整个结肠活检组织的蛋白质组特征进行描述,并应用基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF MS)的肽质量指纹图谱进行鉴定差异表达的蛋白质斑点。

结果

通过图像分析注释了 597 个斑点,其中 222 个斑点在患者组中炎症和非炎症组织之间的蛋白质水平存在统计学差异。主成分分析清楚地将非炎症样本与炎症样本分开,表明急性 UC 结肠黏膜的蛋白质组特征很强。总共鉴定了 43 个单独的蛋白质斑点,包括参与能量代谢(磷酸丙糖异构酶、甘油-3-磷酸脱氢酶、α烯醇酶和 L-乳酸脱氢酶 B 链)和氧化应激(超氧化物歧化酶、硫氧还蛋白和硒结合蛋白)的蛋白质。

结论

发现 UC 患者炎症组织存在独特的蛋白质组特征。鉴定出参与能量代谢和氧化应激的特定蛋白质可能是 UC 的潜在候选标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05d2/3441502/1b24439b9fd0/1471-230X-12-76-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05d2/3441502/a088d95b7ecb/1471-230X-12-76-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05d2/3441502/f7308c278938/1471-230X-12-76-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05d2/3441502/1b24439b9fd0/1471-230X-12-76-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05d2/3441502/a088d95b7ecb/1471-230X-12-76-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05d2/3441502/f7308c278938/1471-230X-12-76-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05d2/3441502/1b24439b9fd0/1471-230X-12-76-3.jpg

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本文引用的文献

1
The role of reactive oxygen metabolites in ulcerative colitis.活性氧代谢物在溃疡性结肠炎中的作用。
Inflamm Bowel Dis. 1997 Winter;3(4):260-4.
2
Proteomics at the interface of psychology, gut physiology and dysfunction: an underexploited approach that deserves expansion.蛋白质组学在心理学、肠道生理学和功能障碍之间的界面:一种值得扩展的未充分利用的方法。
Expert Rev Proteomics. 2011 Oct;8(5):605-14. doi: 10.1586/epr.11.50.
3
Biospecimen reporting for improved study quality (BRISQ).生物标本报告改进研究质量(BRISQ)。
狼疮疾病发作期间纵向肠道微生物组分析和致病性菌株的爆发。
Ann Rheum Dis. 2023 Oct;82(10):1315-1327. doi: 10.1136/ard-2023-223929. Epub 2023 Jun 26.
4
A Current State of Proteomics in Adult and Pediatric Inflammatory Bowel Diseases: A Systematic Search and Review.蛋白质组学在成人和儿童炎症性肠病中的现状:系统检索和综述。
Int J Mol Sci. 2023 May 27;24(11):9386. doi: 10.3390/ijms24119386.
5
Loss of Peroxiredoxin IV Protects Mice from Azoxymethane/Dextran Sulfate Sodium-Induced Colorectal Cancer Development.过氧化物酶体增殖物激活受体IV缺失可保护小鼠免受氧化偶氮甲烷/葡聚糖硫酸钠诱导的结直肠癌发展。
Antioxidants (Basel). 2023 Mar 9;12(3):677. doi: 10.3390/antiox12030677.
6
Essential Roles of Peroxiredoxin IV in Inflammation and Cancer.过氧化物酶 4 在炎症和癌症中的基本作用
Molecules. 2022 Oct 2;27(19):6513. doi: 10.3390/molecules27196513.
7
Proteomic characterisations of ulcerative colitis endoscopic biopsies associate with clinically relevant histological measurements of disease severity.溃疡性结肠炎内镜活检的蛋白质组学特征与临床相关的疾病严重程度组织学测量相关。
J Clin Pathol. 2022 Sep;75(9):636-642. doi: 10.1136/jclinpath-2021-207718. Epub 2021 Aug 5.
8
Assessment of the usefulness of imaging studies and biomarkers in the activity of Crohn's disease.评估影像学检查和生物标志物在克罗恩病活动中的有用性。
Prz Gastroenterol. 2021;16(1):15-22. doi: 10.5114/pg.2020.93539. Epub 2020 Mar 9.
9
Oxidative Stress Markers in Inflammatory Bowel Diseases: Systematic Review.炎症性肠病中的氧化应激标志物:系统评价
Diagnostics (Basel). 2020 Aug 17;10(8):601. doi: 10.3390/diagnostics10080601.
10
New Insights into Inflammatory Bowel Diseases from Proteomic and Lipidomic Studies.蛋白质组学和脂质组学研究对炎症性肠病的新见解
Proteomes. 2020 Aug 10;8(3):18. doi: 10.3390/proteomes8030018.
J Proteome Res. 2011 Aug 5;10(8):3429-38. doi: 10.1021/pr200021n. Epub 2011 Jun 21.
4
The utility of biomarkers in the diagnosis and therapy of inflammatory bowel disease.生物标志物在炎症性肠病的诊断和治疗中的应用。
Gastroenterology. 2011 May;140(6):1817-1826.e2. doi: 10.1053/j.gastro.2010.11.058.
5
Genetics of ulcerative colitis.溃疡性结肠炎的遗传学。
Inflamm Bowel Dis. 2011 Mar;17(3):831-48. doi: 10.1002/ibd.21375. Epub 2010 Nov 12.
6
Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.荟萃分析确定了 29 个额外的溃疡性结肠炎风险位点,使已确认的关联数量增加到 47 个。
Nat Genet. 2011 Mar;43(3):246-52. doi: 10.1038/ng.764. Epub 2011 Feb 6.
7
Polymorphisms in NF-κB, PXR, LXR, PPARγ and risk of inflammatory bowel disease.NF-κB、PXR、LXR、PPARγ 基因多态性与炎症性肠病的易感性研究
World J Gastroenterol. 2011 Jan 14;17(2):197-206. doi: 10.3748/wjg.v17.i2.197.
8
Cyclooxygenase-2 (COX-2) polymorphisms and risk of inflammatory bowel disease in a Scottish and Danish case-control study.环氧化酶-2(COX-2)多态性与苏格兰和丹麦病例对照研究中炎症性肠病的风险。
Inflamm Bowel Dis. 2011 Apr;17(4):937-46. doi: 10.1002/ibd.21440. Epub 2010 Aug 27.
9
The polymorphism rs3024505 proximal to IL-10 is associated with risk of ulcerative colitis and Crohns disease in a Danish case-control study.丹麦病例对照研究表明,IL-10 近端 rs3024505 多态性与溃疡性结肠炎和克罗恩病的发病风险相关。
BMC Med Genet. 2010 May 28;11:82. doi: 10.1186/1471-2350-11-82.
10
New proteomic approaches for biomarker discovery in inflammatory bowel disease.用于炎症性肠病生物标志物发现的新蛋白质组学方法。
Inflamm Bowel Dis. 2010 Jul;16(7):1239-46. doi: 10.1002/ibd.21212.