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鼠与人:支气管肺泡液的比较蛋白质组学。

Of mice and men: comparative proteomics of bronchoalveolar fluid.

机构信息

Center for Lung Biology, Division of Pulmonary and Critical Care Medicine, Seattle, WA, USA.

出版信息

Eur Respir J. 2010 Jun;35(6):1388-95. doi: 10.1183/09031936.00089409. Epub 2009 Dec 23.

Abstract

We hypothesised that comparing the protein mixture in bronchoalveolar lavage fluid (BALF) between humans and mice may lead to mechanistic insights into common and divergent pathways that evolved in each species. BALF from four humans and six mice was pooled separately and underwent identical shotgun proteomic analysis. Functional and network analysis was applied to identify overlapping and distinct pathways enriched in the BALF. Follow-up experiments using Western analysis in unpooled BALF samples were performed. We identified 91 unique proteins in human and 117 unique proteins in mouse BALF samples. Functional analysis of the proteins revealed conservation of several key processes between the species, including defence response. Oxidative stress response, however, was selectively enriched only in mouse BALF. Differences in the expression of peroxiredoxin-1, a key member of the defence pathway against oxidative injury, were confirmed between normal human and mouse BALF and in models of lung injury. A computational proteomics approach of mouse and human BALF confirms the conservation of immune and defence-mediated pathways while highlighting differences in response to oxidative stress. These observations suggest that the use of mice models to study human lung disorders should be undertaken with an appreciation of interspecies variability.

摘要

我们假设,比较人类和小鼠的支气管肺泡灌洗液(BALF)中的蛋白质混合物,可能会深入了解在每个物种中进化的共同和不同的途径。分别对 4 名人类和 6 名小鼠的 BALF 进行混合,并对其进行相同的鸟枪法蛋白质组学分析。应用功能和网络分析来识别在 BALF 中富集的重叠和独特途径。使用未混合的 BALF 样本进行 Western 分析的后续实验。我们在人类 BALF 样本中鉴定出 91 种独特蛋白质,在小鼠 BALF 样本中鉴定出 117 种独特蛋白质。蛋白质的功能分析表明,几个关键过程在物种间具有保守性,包括防御反应。然而,氧化应激反应仅在小鼠 BALF 中选择性富集。在正常人和小鼠 BALF 以及肺损伤模型中,防御途径中关键成员过氧化物酶 1 的表达差异得到了证实。对小鼠和人类 BALF 的计算蛋白质组学方法证实了免疫和防御介导途径的保守性,同时突出了对氧化应激反应的差异。这些观察结果表明,在使用小鼠模型研究人类肺部疾病时,应考虑种间变异性。

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