丙烯醛暴露后moesin的蛋白质组学鉴定。

IF 2.1 3区 生物学 Q3 BIOCHEMICAL RESEARCH METHODS
Proteome Science Pub Date : 2018-01-17 eCollection Date: 2018-01-01 DOI:10.1186/s12953-017-0130-4
Pureun-Haneul Lee, Byeong-Gon Kim, Sun-Hye Lee, George D Leikauf, An-Soo Jang
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引用次数: 1

摘要

背景:丙烯醛(烯丙醛)作为烟雾刺激物之一,可加重慢性气道疾病,并在哮喘和慢性阻塞性肺疾病患者的痰液中增加。但潜在的机制仍未解决。研究的目的是鉴定丙烯醛暴露的人肺微血管内皮细胞(HMVEC-L)中的蛋白表达。方法:采用蛋白质组学方法测定丙烯醛30 nM和300 nM作用于hvec - l后8 h和24 h的蛋白表达情况。丙烯醛30 nM和300 nM处理HMVEC-L后,在二维凝胶上改变了21个蛋白点,用MALDI-TOF ms对其进行了分析。结果:这些蛋白包括抗氧化、信号转导、细胞骨架、蛋白转导、催化还原等。根据蛋白表达模式的时间进程将其分为持续增加、短暂增加、短暂减少和持续减少四组。为验证,对丙烯醛暴露小鼠肺组织进行免疫组化染色和Western blotting。与假处理小鼠相比,丙烯醛暴露小鼠的内皮细胞、上皮细胞和炎症细胞均表达Moesin,肺组织中Moesin表达增加。结论:这些结果提示一些蛋白质可能在丙烯醛暴露引起的气道疾病恶化中起重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Proteomic identification of moesin upon exposure to acrolein.

Proteomic identification of moesin upon exposure to acrolein.

Proteomic identification of moesin upon exposure to acrolein.

Proteomic identification of moesin upon exposure to acrolein.

Background: Acrolein (allyl Aldehyde) as one of smoke irritant exacerbates chronic airway diseases and increased in sputum of patients with asthma and chronic obstructive lung disease. But underlying mechanism remains unresolved. The aim of study was to identify protein expression in human lung microvascular endothelial cells (HMVEC-L) exposed to acrolein.

Methods: A proteomic approach was used to determine the different expression of proteins at 8 h and 24 h after treatment of acrolein 30 nM and 300 nM to HMVEC-L. Treatment of HMVEC-L with acrolein 30 nM and 300 nM altered 21 protein spots on the two-dimensional gel, and these were then analyzed by MALDI-TOF MS.

Results: These proteins included antioxidant, signal transduction, cytoskeleton, protein transduction, catalytic reduction. The proteins were classified into four groups according to the time course of their expression patterns such as continually increasing, transient increasing, transient decreasing, and continually decreasing. For validation immunohistochemical staining and Western blotting was performed on lung tissues from acrolein exposed mice. Moesin was expressed in endothelium, epithelium, and inflammatory cells and increased in lung tissues of acrolein exposed mice compared with sham treated mice.

Conclusions: These results indicate that some of proteins may be an important role for airway disease exacerbation caused by acrolein exposure.

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来源期刊
Proteome Science
Proteome Science 生物-生化研究方法
CiteScore
2.90
自引率
0.00%
发文量
17
审稿时长
4.5 months
期刊介绍: Proteome Science is an open access journal publishing research in the area of systems studies. Proteome Science considers manuscripts based on all aspects of functional and structural proteomics, genomics, metabolomics, systems analysis and metabiome analysis. It encourages the submissions of studies that use large-scale or systems analysis of biomolecules in a cellular, organismal and/or environmental context. Studies that describe novel biological or clinical insights as well as methods-focused studies that describe novel methods for the large-scale study of any and all biomolecules in cells and tissues, such as mass spectrometry, protein and nucleic acid microarrays, genomics, next-generation sequencing and computational algorithms and methods are all within the scope of Proteome Science, as are electron topography, structural methods, proteogenomics, chemical proteomics, stem cell proteomics, organelle proteomics, plant and microbial proteomics. In spite of its name, Proteome Science considers all aspects of large-scale and systems studies because ultimately any mechanism that results in genomic and metabolomic changes will affect or be affected by the proteome. To reflect this intrinsic relationship of biological systems, Proteome Science will consider all such articles.
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