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囊性纤维化小鼠经鼻腔接种后易反复发生急性肺炎。

Cystic Fibrosis Mice Are Highly Susceptible to Repeated Acute Pneumonia after Intranasal Inoculation.

机构信息

Department of Anesthesiology, Critical Care and Pain Medicine, Cardiac Anesthesia Division, Boston Children's Hospital, Boston, USA.

Department of Anaesthesia, Harvard Medical School, Boston, USA.

出版信息

Biomed Res Int. 2024 Feb 5;2024:4769779. doi: 10.1155/2024/4769779. eCollection 2024.

DOI:10.1155/2024/4769779
PMID:38347907
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10861279/
Abstract

Cystic fibrosis (CF) is a genetic disorder caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) that controls chloride current. A number of different CFTR transgenic mouse lines have been developed and subjected to both acute and chronic infection models. However, prior studies showed no substantial differences in bacterial clearance between CF and non-CF mice after single inoculations. Here, using F508del transgenic CF mice, we examined the role of repeated acute (PA) infection, with the second inoculation 7 days after the first. We found that CF mice were more susceptible to PA infection than non-CF mice following the second inoculation, with non-CF mice showing better neutrophil recruitment and effector functions. We further investigated the characteristics of lung immune cells using single-cell RNA sequencing, finding that non-CF lung neutrophils had more prominent upregulation of adhesion molecules including intercellular adhesion molecule-1 (ICAM-1) compared to CF lung neutrophils. Although people with CF are often colonized with bacteria and have high numbers of neutrophils in the airways during chronic infection, these data suggest that CF neutrophils have deficient effector functions in the setting of repeated acute infection.

摘要

囊性纤维化 (CF) 是一种由囊性纤维化跨膜电导调节因子 (CFTR) 基因突变引起的遗传性疾病,该基因控制氯离子电流。已经开发了许多不同的 CFTR 转基因小鼠品系,并对其进行了急性和慢性感染模型的研究。然而,先前的研究表明,在单次接种后,CF 和非 CF 小鼠之间的细菌清除没有明显差异。在这里,我们使用 F508del 转基因 CF 小鼠,研究了反复急性 (PA) 感染的作用,第二次接种是在第一次接种后 7 天进行的。我们发现,第二次接种后,CF 小鼠比非 CF 小鼠更容易受到 PA 感染,而非 CF 小鼠显示出更好的中性粒细胞募集和效应功能。我们进一步使用单细胞 RNA 测序研究了肺免疫细胞的特征,发现非 CF 肺中性粒细胞中包括细胞间黏附分子-1 (ICAM-1) 在内的黏附分子的上调更为显著,而 CF 肺中性粒细胞的效应功能则存在缺陷。尽管 CF 患者在慢性感染期间经常被细菌定植,并且气道中中性粒细胞数量较高,但这些数据表明,CF 中性粒细胞在反复急性感染的情况下,其效应功能存在缺陷。

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本文引用的文献

1
Age-dependent transcriptomic profiles of leukocytes in pediatric population.儿童人群中性粒细胞转录组随年龄变化的特征。
Clin Immunol. 2023 Oct;255:109728. doi: 10.1016/j.clim.2023.109728. Epub 2023 Aug 9.
2
Cystic Fibrosis: A Review.囊性纤维化:综述。
JAMA. 2023 Jun 6;329(21):1859-1871. doi: 10.1001/jama.2023.8120.
3
Pharmacologic improvement of CFTR function rapidly decreases sputum pathogen density, but lung infections generally persist.药物改善 CFTR 功能可迅速降低痰中病原体密度,但肺部感染通常持续存在。
J Clin Invest. 2023 May 15;133(10):e167957. doi: 10.1172/JCI167957.
4
DAVID: a web server for functional enrichment analysis and functional annotation of gene lists (2021 update).DAVID:一个用于基因列表功能富集分析和功能注释的网络服务器(2021 更新)。
Nucleic Acids Res. 2022 Jul 5;50(W1):W216-W221. doi: 10.1093/nar/gkac194.
5
Altered Degranulation and pH of Neutrophil Phagosomes Impacts Antimicrobial Efficiency in Cystic Fibrosis.中性粒细胞吞噬体脱粒和 pH 值改变影响囊性纤维化中的抗菌效率。
Front Immunol. 2020 Dec 18;11:600033. doi: 10.3389/fimmu.2020.600033. eCollection 2020.
6
Animal and Cell Culture Models for Cystic Fibrosis: Which Model Is Right for Your Application?动物和细胞培养模型在囊性纤维化研究中的应用:哪种模型适合您的应用?
Am J Pathol. 2021 Feb;191(2):228-242. doi: 10.1016/j.ajpath.2020.10.017. Epub 2020 Nov 21.
7
Protease inhibitors elicit anti-inflammatory effects in CF mice with Pseudomonas aeruginosa acute lung infection.蛋白酶抑制剂可在铜绿假单胞菌急性肺部感染的 CF 小鼠中发挥抗炎作用。
Clin Exp Immunol. 2021 Jan;203(1):87-95. doi: 10.1111/cei.13518. Epub 2020 Oct 12.
8
Volatile anesthetics isoflurane and sevoflurane directly target and attenuate Toll-like receptor 4 system.挥发性麻醉剂异氟烷和七氟烷直接靶向并减弱 Toll 样受体 4 系统。
FASEB J. 2019 Dec;33(12):14528-14541. doi: 10.1096/fj.201901570R. Epub 2019 Nov 2.
9
Complete Genome Sequence of Pseudomonas aeruginosa Reference Strain PAK.铜绿假单胞菌参考菌株PAK的全基因组序列
Microbiol Resour Announc. 2019 Oct 10;8(41):e00865-19. doi: 10.1128/MRA.00865-19.
10
Dysregulated Calcium Homeostasis in Cystic Fibrosis Neutrophils Leads to Deficient Antimicrobial Responses.囊性纤维化中性粒细胞钙稳态失调导致抗菌反应缺陷。
J Immunol. 2018 Oct 1;201(7):2016-2027. doi: 10.4049/jimmunol.1800076. Epub 2018 Aug 17.