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主流香烟烟雾会影响小鼠声带上皮和黏液屏障。

Mainstream Cigarette Smoke Impacts the Mouse Vocal Fold Epithelium and Mucus Barrier.

机构信息

Department of Otolaryngology - Head & Neck Surgery, Stanford University School of Medicine, Stanford, California, U.S.A.

出版信息

Laryngoscope. 2021 Nov;131(11):2530-2539. doi: 10.1002/lary.29572. Epub 2021 Apr 17.

DOI:10.1002/lary.29572
PMID:33864646
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8502200/
Abstract

OBJECTIVES/HYPOTHESIS: Cigarette smoke (CS) is a primary risk factor for the development of numerous benign and malignant laryngeal diseases. The epithelium and mucus lining the vocal folds (VF) are the first barriers against CS. The primary objective of this study was to investigate epithelial and mucus barrier changes in the mouse laryngeal mucosa upon exposure to subacute CS. The secondary objective was to compare mucus barrier changes in mice and human smokers and nonsmokers. Study Design Animal model.

METHODS

Mice were exposed to CS for 4 weeks for 4 hours (N = 12, high dose [HD]) or 1 hour (N = 12, low dose [LD]) per day. Air-exposed mice were used as a control group (N = 10). Larynges were harvested and VF epithelial barrier integrity was evaluated including cellular proliferation and expression of cell junctions. We also investigated mucus production by examining mucus cell area and mucin expression in mice and human smokers and nonsmokers.

RESULTS

HD CS increased VF epithelial cellular proliferation but did not alter the expression of cell junctions. HD CS also induced hypertrophy of the mucus-producing submucosal glands. However, only LD CS increased MUC5AC gene expression. MUC5AC staining appeared elevated in laryngeal specimens from smokers, but this was not significant as compared to nonsmokers.

CONCLUSIONS

These findings help us identify potential adaptive mechanisms to CS exposure as well as set the foundation for further study of key aspects of epithelial and mucus barrier integrity that may be implicated in laryngeal disease development following prolonged smoking.

LEVEL OF EVIDENCE

NA Laryngoscope, 131:2530-2539, 2021.

摘要

目的/假设:香烟烟雾(CS)是许多良性和恶性喉病发展的主要危险因素。声带(VF)的上皮和黏膜衬里是抵御 CS 的第一道屏障。本研究的主要目的是研究亚急性 CS 暴露后小鼠喉黏膜上皮和黏液屏障的变化。次要目的是比较吸烟和非吸烟的人和小鼠的黏液屏障变化。

研究设计

动物模型。

方法

小鼠每天暴露于 CS 中 4 小时(高剂量 [HD],N=12)或 1 小时(低剂量 [LD],N=12),持续 4 周。空气暴露的小鼠作为对照组(N=10)。采集喉组织,评估 VF 上皮屏障完整性,包括细胞增殖和细胞连接的表达。我们还通过检测小鼠和吸烟及非吸烟人群中黏液细胞面积和黏蛋白表达,研究了黏液产生情况。

结果

HD CS 增加了 VF 上皮细胞的增殖,但不改变细胞连接的表达。HD CS 还诱导了产生黏液的黏膜下腺的肥大。然而,只有 LD CS 增加了 MUC5AC 基因的表达。与非吸烟者相比,吸烟者的喉部标本中 MUC5AC 染色似乎升高,但差异无统计学意义。

结论

这些发现有助于我们确定对 CS 暴露的潜在适应机制,并为进一步研究可能与长期吸烟后喉病发展有关的上皮和黏液屏障完整性的关键方面奠定基础。

证据水平

无 喉镜,131:2530-2539,2021。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e865/8502200/34100209d206/nihms-1707743-f0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e865/8502200/8ef7c144a004/nihms-1707743-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e865/8502200/2f8b3aefb8e5/nihms-1707743-f0002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e865/8502200/a81a27d07742/nihms-1707743-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e865/8502200/ba10f04dd143/nihms-1707743-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e865/8502200/4f4a427670e6/nihms-1707743-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e865/8502200/af9509eea29b/nihms-1707743-f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e865/8502200/34100209d206/nihms-1707743-f0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e865/8502200/8ef7c144a004/nihms-1707743-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e865/8502200/2f8b3aefb8e5/nihms-1707743-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e865/8502200/db60ef53c45a/nihms-1707743-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e865/8502200/a81a27d07742/nihms-1707743-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e865/8502200/ba10f04dd143/nihms-1707743-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e865/8502200/4f4a427670e6/nihms-1707743-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e865/8502200/af9509eea29b/nihms-1707743-f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e865/8502200/34100209d206/nihms-1707743-f0008.jpg

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