Response biomarkers of inhalation exposure to cigarette smoke in the mouse lung.

IF 0.9 4区 医学 Q4 PATHOLOGY Journal of Toxicologic Pathology Pub Date : 2022-07-01 Epub Date: 2022-05-21 DOI:10.1293/tox.2021-0077
Shugo Suzuki, Kazuhisa Asai, Min Gi, Kazuya Kojima, Anna Kakehashi, Yuji Oishi, Taisuke Matsue, Nao Yukimatsu, Kazuto Hirata, Tomoya Kawaguchi, Hideki Wanibuchi
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引用次数: 1

Abstract

Cigarette smoking is known to increase the risk of cancer and chronic obstructive pulmonary disease (COPD). In this study, we evaluated the effects of short-term nose-only inhalation exposure to cigarette smoke in mice. Male 10-week-old C57BL mice were exposed to clean air (control) or mainstream cigarette smoke for 1 h/day, 5 days/week, for 2 or 4 weeks. Exposure to cigarette smoke increased the number of inflammatory cells, especially neutrophils, in the bronchoalveolar lavage fluid, increased inflammatory cell infiltration foci, and caused an increase in the thickness of the peripheral bronchial epithelium. Microarray gene expression analysis indicated that smoke exposure induced inflammatory responses, including leukocyte migration and activation of phagocytes and myeloid cells, as early as two weeks after the initiation of exposure. Importantly, chemokine (C-C motif) ligand 17, resistin-like alpha, and lipocalin 2 were upregulated and may serve as useful markers of the toxic effects of exposure to cigarette smoke before pulmonary histological changes become evident.

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小鼠肺部吸入暴露于香烟烟雾的反应生物标志物。
众所周知,吸烟会增加患癌症和慢性阻塞性肺病(COPD)的风险。在这项研究中,我们评估了短期仅用鼻子吸入香烟烟雾对小鼠的影响。将10周龄雄性C57BL小鼠分别暴露于清洁空气(对照)或主流香烟烟雾中1小时/天、5天/周、2周或4周。暴露于香烟烟雾中,支气管肺泡灌洗液中炎症细胞,特别是中性粒细胞的数量增加,炎症细胞浸润灶增加,并引起支气管周围上皮厚度增加。微阵列基因表达分析表明,烟雾暴露诱导炎症反应,包括白细胞迁移和吞噬细胞和骨髓细胞的激活,早在暴露开始后两周。重要的是,趋化因子(C-C基序)配体17、抵抗素样α和脂质体蛋白2上调,可能在肺部组织学改变变得明显之前作为暴露于香烟烟雾的毒性作用的有用标记。
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来源期刊
Journal of Toxicologic Pathology
Journal of Toxicologic Pathology PATHOLOGY-TOXICOLOGY
CiteScore
2.10
自引率
16.70%
发文量
22
审稿时长
>12 weeks
期刊介绍: JTP is a scientific journal that publishes original studies in the field of toxicological pathology and in a wide variety of other related fields. The main scope of the journal is listed below. Administrative Opinions of Policymakers and Regulatory Agencies Adverse Events Carcinogenesis Data of A Predominantly Negative Nature Drug-Induced Hematologic Toxicity Embryological Pathology High Throughput Pathology Historical Data of Experimental Animals Immunohistochemical Analysis Molecular Pathology Nomenclature of Lesions Non-mammal Toxicity Study Result or Lesion Induced by Chemicals of Which Names Hidden on Account of the Authors Technology and Methodology Related to Toxicological Pathology Tumor Pathology; Neoplasia and Hyperplasia Ultrastructural Analysis Use of Animal Models.
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