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首页> 外文期刊>Inhalation toxicology >Effects of subchronic exposures to concentrated ambient particles (CAPs) in mice. VI. Gene expression in heart and lung tissue.
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Effects of subchronic exposures to concentrated ambient particles (CAPs) in mice. VI. Gene expression in heart and lung tissue.

机译:亚慢性暴露于小鼠集中环境颗粒(CAP)的影响。 VI。心脏和肺组织中的基因表达。

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The purpose of this exploratory study within the integrated subchronic inhalation exposure study (Lippmann et al., 2005) was to identify genes in heart and lung tissue that changed in expression level as a result of subchronic exposure to concentrated ambient particles (CAPs). Identification of CAPs exposure-related changes in gene expression could serve in the formulation of mechanistic hypotheses and/or to suggest possible biomarkers of exposure. In this exploratory study undertaken here, tissues from multiple replicates of ApoE/low-density-lipoprotein double knockout (DK) mice were examined for relative exposure-related changes in gene expression. Due to limited resources, the number of replicates was three for each tissue (lung and heart) of each exposure condition (CAPs or air control). A rigorous comparison of exposure versus control data using the "significance analysis of microarrays" (SAM) method indicated that only one gene was differentially expressed at a significant level. However, when using a less restrictive, nonstatistical analytical treatment of the data, several genes that might be involved in PM-related heart or lung pathology, and/or the circadian rhythm of physiological processes, were identified. A more comprehensive study is required to mre definitively assess differences in gene expression in heart and lung resulting from exposure to CAPs.
机译:这项综合性亚慢性吸入暴露研究(Lippmann等,2005)中的探索性研究的目的是鉴定心脏和肺组织中由于亚慢性暴露于集中环境颗粒(CAPs)而导致表达水平发生变化的基因。 CAPs暴露相关基因表达变化的鉴定可用于机制假设的提出和/或提示可能的暴露生物标志物。在这里进行的这项探索性研究中,检查了来自ApoE /低密度脂蛋白双敲除(DK)小鼠多个复制品的组织中基因表达的相对暴露相关变化。由于资源有限,每种暴露条件(CAP或空气控制)的每个组织(肺和心脏)的重复次数均为3。使用“微阵列的显着性分析”(SAM)方法对暴露数据与对照数据进行严格比较,结果表明只有一个基因在显着水平上差异表达。但是,当使用数据的限制较少的非统计分析处理时,已确定了可能与PM相关的心脏或肺部病理和/或生理过程的昼夜节律有关的几个基因。需要更全面的研究以明确评估由于暴露于CAP而导致的心脏和肺部基因表达的差异。

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