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吸烟人群中气道上皮细胞与肺泡巨噬细胞的氧化应激基因表达存在差异。

Disparate oxidant gene expression of airway epithelium compared to alveolar macrophages in smokers.

机构信息

Department of Genetic Medicine, Weill Cornell Medical College, New York, New York, USA.

出版信息

Respir Res. 2009 Nov 17;10(1):111. doi: 10.1186/1465-9921-10-111.

Abstract

BACKGROUND

The small airway epithelium and alveolar macrophages are exposed to oxidants in cigarette smoke leading to epithelial dysfunction and macrophage activation. In this context, we asked: what is the transcriptome of oxidant-related genes in small airway epithelium and alveolar macrophages, and does their response differ substantially to inhaled cigarette smoke?

METHODS

Using microarray analysis, with TaqMan RT-PCR confirmation, we assessed oxidant-related gene expression in small airway epithelium and alveolar macrophages from the same healthy nonsmoker and smoker individuals.

RESULTS

Of 155 genes surveyed, 87 (56%) were expressed in both cell populations in nonsmokers, with higher expression in alveolar macrophages (43%) compared to airway epithelium (24%). In smokers, there were 15 genes (10%) up-regulated and 7 genes (5%) down-regulated in airway epithelium, but only 3 (2%) up-regulated and 2 (1%) down-regulated in alveolar macrophages. Pathway analysis of airway epithelium showed oxidant pathways dominated, but in alveolar macrophages immune pathways dominated.

CONCLUSION

Thus, the response of different cell-types with an identical genome exposed to the same stress of smoking is different; responses of alveolar macrophages are more subdued than those of airway epithelium. These findings are consistent with the observation that, while the small airway epithelium is vulnerable, alveolar macrophages are not "diseased" in response to smoking.

TRIAL REGISTRATION

ClinicalTrials.gov ID: NCT00224185 and NCT00224198.

摘要

背景

小气道上皮细胞和肺泡巨噬细胞暴露于香烟烟雾中的氧化剂中,导致上皮细胞功能障碍和巨噬细胞活化。在这种情况下,我们提出了以下问题:小气道上皮细胞和肺泡巨噬细胞中与氧化剂相关的基因的转录组是什么,它们对吸入的香烟烟雾的反应是否有很大的不同?

方法

我们使用微阵列分析,并结合 TaqMan RT-PCR 确认,评估了来自同一健康不吸烟者和吸烟者的小气道上皮细胞和肺泡巨噬细胞中与氧化剂相关的基因表达。

结果

在调查的 155 个基因中,有 87 个(56%)在不吸烟者的两种细胞群体中表达,肺泡巨噬细胞中的表达(43%)高于气道上皮细胞(24%)。在吸烟者中,气道上皮细胞中有 15 个基因(10%)上调,7 个基因(5%)下调,但肺泡巨噬细胞中只有 3 个(2%)上调和 2 个(1%)下调。气道上皮细胞的通路分析表明,氧化剂通路占主导地位,但在肺泡巨噬细胞中,免疫通路占主导地位。

结论

因此,暴露于相同吸烟应激的不同细胞类型的相同基因组的反应是不同的;肺泡巨噬细胞的反应比气道上皮细胞的反应更为温和。这些发现与以下观察结果一致,即虽然小气道上皮细胞很脆弱,但肺泡巨噬细胞在吸烟反应中没有“患病”。

试验注册

ClinicalTrials.gov 注册号:NCT00224185 和 NCT00224198。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a56e/2787510/708627f72675/1465-9921-10-111-1.jpg

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本文引用的文献

1
The Effect of Cigarette Smoke-derived Oxidants on the Inflammatory Response of the Lung.
Clin Appl Immunol Rev. 2006 Jan 1;6(1):53-72. doi: 10.1016/j.cair.2006.04.002.
2
Genetic variation and gene expression in antioxidant related enzymes and risk of COPD: a systematic review.
Thorax. 2008 Nov;63(11):956-61. doi: 10.1136/thx.2007.086199. Epub 2008 Jun 19.
3
Altered Nrf2/Keap1-Bach1 equilibrium in pulmonary emphysema.
Thorax. 2008 Oct;63(10):916-24. doi: 10.1136/thx.2007.091181. Epub 2008 Jun 17.
4
Decline in NRF2-regulated antioxidants in chronic obstructive pulmonary disease lungs due to loss of its positive regulator, DJ-1.
Am J Respir Crit Care Med. 2008 Sep 15;178(6):592-604. doi: 10.1164/rccm.200803-380OC. Epub 2008 Jun 12.
5
IL-10: the master regulator of immunity to infection.
J Immunol. 2008 May 1;180(9):5771-7. doi: 10.4049/jimmunol.180.9.5771.
6
Expression of genes involved in oxidative stress responses in airway epithelial cells of smokers with chronic obstructive pulmonary disease.
Am J Respir Crit Care Med. 2007 Mar 15;175(6):577-86. doi: 10.1164/rccm.200607-931OC. Epub 2006 Dec 7.
7
Modification of gene expression of the small airway epithelium in response to cigarette smoking.
J Mol Med (Berl). 2007 Jan;85(1):39-53. doi: 10.1007/s00109-006-0103-z. Epub 2006 Nov 8.
8
Airway epithelial stem cells and the pathophysiology of chronic obstructive pulmonary disease.
Proc Am Thorac Soc. 2006 Nov;3(8):718-25. doi: 10.1513/pats.200605-117SF.
9
Cytochrome P450 4F subfamily: at the crossroads of eicosanoid and drug metabolism.
Pharmacol Ther. 2006 Dec;112(3):589-611. doi: 10.1016/j.pharmthera.2006.03.008. Epub 2006 Aug 22.

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