• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

UPM 暴露的上皮细胞与巨噬细胞和树突状细胞共培养在阻塞性肺疾病中的 RNA-Seq 分析。

RNA-Seq Analysis of UPM-Exposed Epithelium Co-Cultivated with Macrophages and Dendritic Cells in Obstructive Lung Diseases.

机构信息

Department of Internal Medicine, Pulmonary Diseases and Allergy, Medical University of Warsaw, 02-091 Warsaw, Poland.

Postgraduate School of Molecular Medicine, Medical University of Warsaw, 02-091 Warsaw, Poland.

出版信息

Int J Mol Sci. 2022 Aug 15;23(16):9125. doi: 10.3390/ijms23169125.

DOI:10.3390/ijms23169125
PMID:36012391
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9408857/
Abstract

BACKGROUND

Elevated concentrations of airborne pollutants are correlated with an enlarged rate of obstructive lung disease morbidity as well as acute disease exacerbations. This study aimed to analyze the epithelium mRNA profile in response to airborne particulate matter in the control, asthma, and COPD groups.

RESULTS

A triple co-culture of nasal epithelium, monocyte-derived macrophages, and monocyte-derived dendritic cells obtained from the controls, asthma, and COPD were exposed to urban particulate matter (UPM) for 24 h. RNA-Seq analysis found differences in seven (CYP1B1, CYP1B1-AS1, NCF1, ME1, LINC02029, BPIFA2, EEF1A2), five (CYP1B1, ARC, ENPEP, RASD1, CYP1B1-AS1), and six (CYP1B1, CYP1B1-AS1, IRF4, ATP1B2, TIPARP, CCL22) differentially expressed genes between UPM exposed and unexposed triple co-cultured epithelium in the control, asthma, and COPD groups, respectively. PCR analysis showed that mRNA expression of BPIFA2 and ENPEP was upregulated in both asthma and COPD, while the expression of CYP1B1-AS1 and TIPARP was increased in the epithelium from COPD patients only. Biological processes changed in UPM exposed triple co-cultured epithelium were associated with epidermis development and epidermal cell differentiation in asthma and with response to toxic substances in COPD.

CONCLUSIONS

The biochemical processes associated with pathophysiology of asthma and COPD impairs the airway epithelial response to UPM.

摘要

背景

空气中污染物浓度的升高与阻塞性肺部疾病发病率的增加以及急性疾病恶化有关。本研究旨在分析对照、哮喘和 COPD 组中空气中颗粒物作用下的上皮细胞 mRNA 谱。

结果

从对照、哮喘和 COPD 患者中获得的鼻上皮、单核细胞衍生的巨噬细胞和单核细胞衍生的树突状细胞的三重共培养物暴露于城市颗粒物 (UPM) 24 小时。RNA-Seq 分析发现,在对照、哮喘和 COPD 组中,暴露于 UPM 和未暴露于 UPM 的三重共培养上皮细胞之间存在 7 个(CYP1B1、CYP1B1-AS1、NCF1、ME1、LINC02029、BPIFA2、EEF1A2)、5 个(CYP1B1、ARC、ENPEP、RASD1、CYP1B1-AS1)和 6 个(CYP1B1、CYP1B1-AS1、IRF4、ATP1B2、TIPARP、CCL22)差异表达基因。PCR 分析显示,BPIFA2 和 ENPEP 的 mRNA 表达在哮喘和 COPD 中均上调,而 CYP1B1-AS1 和 TIPARP 的表达仅在 COPD 患者的上皮细胞中增加。暴露于 UPM 的三重共培养上皮细胞中改变的生物学过程与哮喘中的表皮发育和表皮细胞分化以及 COPD 中的对有毒物质的反应有关。

结论

与哮喘和 COPD 病理生理学相关的生化过程会损害气道上皮对 UPM 的反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22eb/9408857/48e4361d1283/ijms-23-09125-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22eb/9408857/b19df6770cb9/ijms-23-09125-g0A1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22eb/9408857/7ddaa437991f/ijms-23-09125-g0A2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22eb/9408857/da3caf694692/ijms-23-09125-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22eb/9408857/45abb82e2795/ijms-23-09125-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22eb/9408857/9717d7217cc8/ijms-23-09125-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22eb/9408857/484d74a1294b/ijms-23-09125-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22eb/9408857/5d60b5a4137d/ijms-23-09125-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22eb/9408857/93c1fd594bf1/ijms-23-09125-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22eb/9408857/2f70f3edf6bc/ijms-23-09125-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22eb/9408857/48e4361d1283/ijms-23-09125-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22eb/9408857/b19df6770cb9/ijms-23-09125-g0A1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22eb/9408857/7ddaa437991f/ijms-23-09125-g0A2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22eb/9408857/da3caf694692/ijms-23-09125-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22eb/9408857/45abb82e2795/ijms-23-09125-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22eb/9408857/9717d7217cc8/ijms-23-09125-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22eb/9408857/484d74a1294b/ijms-23-09125-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22eb/9408857/5d60b5a4137d/ijms-23-09125-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22eb/9408857/93c1fd594bf1/ijms-23-09125-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22eb/9408857/2f70f3edf6bc/ijms-23-09125-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22eb/9408857/48e4361d1283/ijms-23-09125-g008.jpg

相似文献

1
RNA-Seq Analysis of UPM-Exposed Epithelium Co-Cultivated with Macrophages and Dendritic Cells in Obstructive Lung Diseases.UPM 暴露的上皮细胞与巨噬细胞和树突状细胞共培养在阻塞性肺疾病中的 RNA-Seq 分析。
Int J Mol Sci. 2022 Aug 15;23(16):9125. doi: 10.3390/ijms23169125.
2
Interactions of nasal epithelium with macrophages and dendritic cells variously alter urban PM-induced inflammation in healthy, asthma and COPD.鼻腔上皮与巨噬细胞和树突状细胞的相互作用可改变健康人群、哮喘和 COPD 患者对城市 PM 诱导的炎症反应。
Sci Rep. 2021 Jun 24;11(1):13259. doi: 10.1038/s41598-021-92626-w.
3
The Expressions of TSLP, IL-33, and IL-17A in Monocyte Derived Dendritic Cells from Asthma and COPD Patients are Related to Epithelial-Macrophage Interactions.哮喘和 COPD 患者来源的树突状细胞中 TSLP、IL-33 和 IL-17A 的表达与上皮-巨噬细胞相互作用有关。
Cells. 2020 Aug 22;9(9):1944. doi: 10.3390/cells9091944.
4
Urban particulate matter in Beijing, China, enhances allergen-induced murine lung eosinophilia.中国北京城市颗粒物增强变应原诱导的小鼠肺部嗜酸性粒细胞增多。
Inhal Toxicol. 2010 Aug;22(9):709-18. doi: 10.3109/08958371003631608.
5
Urban particulate matter induces pro-remodeling factors by airway epithelial cells from healthy and asthmatic children.城市颗粒物通过健康和哮喘儿童的气道上皮细胞诱导促重塑因子。
Inhal Toxicol. 2013 Oct;25(12):653-60. doi: 10.3109/08958378.2013.827283.
6
Tumor necrosis factor-α mediates interactions between macrophages and epithelial cells underlying proinflammatory gene expression induced by particulate matter.肿瘤坏死因子-α介导颗粒物诱导的促炎基因表达中巨噬细胞和上皮细胞之间的相互作用。
Toxicology. 2012 Sep 28;299(2-3):125-32. doi: 10.1016/j.tox.2012.05.014. Epub 2012 May 23.
7
Urban particulate matter stimulation of human dendritic cells enhances priming of naive CD8 T lymphocytes.城市颗粒物刺激人树突状细胞增强幼稚 CD8 T 淋巴细胞的启动。
Immunology. 2018 Apr;153(4):502-512. doi: 10.1111/imm.12852. Epub 2017 Nov 28.
8
Posttranscriptional Gene Regulatory Networks in Chronic Airway Inflammatory Diseases: Mapping of RNA-Binding Protein Expression in Airway Epithelium.慢性气道炎症性疾病中的转录后基因调控网络:气道上皮中RNA结合蛋白表达图谱
Front Immunol. 2020 Oct 16;11:579889. doi: 10.3389/fimmu.2020.579889. eCollection 2020.
9
Epithelial-macrophage-dendritic cell interactions impact alarmins expression in asthma and COPD.上皮细胞-巨噬细胞-树突状细胞相互作用影响哮喘和 COPD 中警报素的表达。
Clin Immunol. 2020 Jun;215:108421. doi: 10.1016/j.clim.2020.108421. Epub 2020 Apr 14.
10
Vitamin D Counteracts an IL-23-Dependent IL-17AIFN-γ Response Driven by Urban Particulate Matter.维生素D可对抗由城市颗粒物驱动的依赖白细胞介素-23的白细胞介素-17A/干扰素-γ反应。
Am J Respir Cell Mol Biol. 2017 Sep;57(3):355-366. doi: 10.1165/rcmb.2016-0409OC.

引用本文的文献

1
LncRNA CYP1B1-AS1 as a clinical biomarker exacerbates sepsis inflammatory response via targeting miR- 18a- 5p.长链非编码RNA CYP1B1-AS1作为一种临床生物标志物,通过靶向miR-18a-5p加剧脓毒症炎症反应。
BMC Immunol. 2025 Apr 16;26(1):32. doi: 10.1186/s12865-025-00712-9.
2
The impaired response of nasal epithelial cells to microplastic stimulation in asthma and COPD.哮喘和慢性阻塞性肺疾病中鼻上皮细胞对微塑料刺激的反应受损。
Sci Rep. 2025 Feb 4;15(1):4242. doi: 10.1038/s41598-025-87242-x.
3
Airborne fine particulate matter exposure induces transcriptomic alterations resembling asthmatic signatures: insights from integrated omics analysis.

本文引用的文献

1
Interactions of nasal epithelium with macrophages and dendritic cells variously alter urban PM-induced inflammation in healthy, asthma and COPD.鼻腔上皮与巨噬细胞和树突状细胞的相互作用可改变健康人群、哮喘和 COPD 患者对城市 PM 诱导的炎症反应。
Sci Rep. 2021 Jun 24;11(1):13259. doi: 10.1038/s41598-021-92626-w.
2
Particulate matter less than 10 μm (PM) activates cancer related genes in lung epithelial cells.小于 10 μm 的颗粒物 (PM) 可激活肺上皮细胞中的癌症相关基因。
Inhal Toxicol. 2020 Nov-Dec;32(13-14):487-493. doi: 10.1080/08958378.2020.1850936. Epub 2020 Dec 7.
3
UniProt: the universal protein knowledgebase in 2021.
暴露于空气中的细颗粒物会引发类似于哮喘特征的转录组改变:综合组学分析的见解。
Environ Epigenet. 2025 Jan 2;11(1):dvae026. doi: 10.1093/eep/dvae026. eCollection 2024.
4
The different response of PM stimulated nasal epithelial spheroids in control, asthma and COPD groups.在对照组、哮喘组和慢性阻塞性肺疾病组中,颗粒物刺激鼻上皮球体的不同反应。
Respir Res. 2025 Jan 8;26(1):8. doi: 10.1186/s12931-025-03097-w.
5
Dynamic and prognostic proteomic associations with FEV decline in chronic obstructive pulmonary disease.慢性阻塞性肺疾病中与第一秒用力呼气容积下降相关的动态和预后蛋白质组学关联
medRxiv. 2024 Aug 8:2024.08.07.24311507. doi: 10.1101/2024.08.07.24311507.
6
IRF4-mediated Treg phenotype switching can aggravate hyperoxia-induced alveolar epithelial cell injury.IRF4 介导的 Treg 表型转换可加重高氧诱导的肺泡上皮细胞损伤。
BMC Pulm Med. 2024 Mar 15;24(1):130. doi: 10.1186/s12890-024-02940-y.
7
On the path to predicting immune responses in the lung: Modeling the pulmonary innate immune system at the air-liquid interface (ALI).在预测肺部免疫反应的道路上:在气液界面(ALI)模拟肺部先天免疫系统。
Eur J Pharm Sci. 2023 Dec 1;191:106596. doi: 10.1016/j.ejps.2023.106596. Epub 2023 Sep 26.
UniProt:2021 年的通用蛋白质知识库。
Nucleic Acids Res. 2021 Jan 8;49(D1):D480-D489. doi: 10.1093/nar/gkaa1100.
4
Downregulation of enhancer RNA EMX2OS is associated with poor prognosis in kidney renal clear cell carcinoma.增强子 RNA EMX2OS 的下调与肾透明细胞癌的不良预后相关。
Aging (Albany NY). 2020 Nov 25;12(24):25865-25877. doi: 10.18632/aging.202151.
5
Ensembl 2021.Ensembl 2021.
Nucleic Acids Res. 2021 Jan 8;49(D1):D884-D891. doi: 10.1093/nar/gkaa942.
6
Epithelial-macrophage-dendritic cell interactions impact alarmins expression in asthma and COPD.上皮细胞-巨噬细胞-树突状细胞相互作用影响哮喘和 COPD 中警报素的表达。
Clin Immunol. 2020 Jun;215:108421. doi: 10.1016/j.clim.2020.108421. Epub 2020 Apr 14.
7
Single cell RNA sequencing of 13 human tissues identify cell types and receptors of human coronaviruses.单细胞 RNA 测序分析 13 个人体组织样本,鉴定出人类冠状病毒的细胞类型和受体。
Biochem Biophys Res Commun. 2020 May 21;526(1):135-140. doi: 10.1016/j.bbrc.2020.03.044. Epub 2020 Mar 19.
8
Air pollution-derived particulate matter dysregulates hepatic Krebs cycle, glucose and lipid metabolism in mice.空气污染衍生的颗粒物扰乱了小鼠肝脏的克雷布斯循环、葡萄糖和脂质代谢。
Sci Rep. 2019 Nov 22;9(1):17423. doi: 10.1038/s41598-019-53716-y.
9
A combined epigenome- and transcriptome-wide association study of the oral masticatory mucosa assigns CYP1B1 a central role for epithelial health in smokers.一项针对口腔咀嚼黏膜的表观基因组和转录组全基因组关联研究将 CYP1B1 确定为吸烟人群中上皮健康的核心因素。
Clin Epigenetics. 2019 Jul 22;11(1):105. doi: 10.1186/s13148-019-0697-y.
10
PM-related DNA damage, cytokinetic defects, and cell death in COPD patients from Chiang Dao district, Chiang Mai, Thailand.泰国清迈昌道地区 COPD 患者与 PM 相关的 DNA 损伤、胞质分裂缺陷和细胞死亡。
Environ Sci Pollut Res Int. 2019 Aug;26(24):25326-25340. doi: 10.1007/s11356-019-05641-w. Epub 2019 Jun 29.