Suzuki Shugo, Asai Kazuhisa, Gi Min, Kojima Kazuya, Kakehashi Anna, Oishi Yuji, Matsue Taisuke, Yukimatsu Nao, Hirata Kazuto, Kawaguchi Tomoya, Wanibuchi Hideki
Department of Molecular Pathology, Osaka Metropolitan University Graduate School of Medicine, 1-4-3 Asahi-machi, Abeno-ku, Osaka 545-8585, Japan.
Department of Respiratory Medicine, Osaka Metropolitan University Graduate School of Medicine, 1-4-3 Asahi-machi, Abeno-ku, Osaka 545-8585, Japan.
J Toxicol Pathol. 2022 Jul;35(3):247-254. doi: 10.1293/tox.2021-0077. Epub 2022 May 21.
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.
众所周知,吸烟会增加患癌症和慢性阻塞性肺疾病(COPD)的风险。在本研究中,我们评估了小鼠短期仅经鼻吸入香烟烟雾的影响。10周龄雄性C57BL小鼠每天暴露于清洁空气(对照组)或主流香烟烟雾中1小时,每周5天,持续2周或4周。暴露于香烟烟雾会增加支气管肺泡灌洗液中炎症细胞的数量,尤其是中性粒细胞,增加炎症细胞浸润灶,并导致外周支气管上皮厚度增加。基因芯片基因表达分析表明,早在暴露开始后两周,烟雾暴露就会引发炎症反应,包括白细胞迁移以及吞噬细胞和髓样细胞的激活。重要的是,趋化因子(C-C基序)配体17、抵抗素样α和脂质运载蛋白2上调,并且在肺部组织学变化明显之前,它们可能作为暴露于香烟烟雾毒性作用的有用标志物。