Suppr超能文献

γδT 细胞在感染伯氏疟原虫的 C57BL/6 小鼠肺部的特征。

Characterization of γδT cells in lung of Plasmodium yoelii-infected C57BL/6 mice.

机构信息

Key Laboratory of Immunology, State Key Laboratory of Respiratory Disease, Guangzhou Institute of Respiratory Health, The First Affliated Hospital of Guangzhou Medical University, Guangzhou, 510120, China.

Biological Resource Center, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, 510120, China.

出版信息

Malar J. 2021 Feb 15;20(1):89. doi: 10.1186/s12936-021-03619-z.

Abstract

BACKGROUND

Malaria has high morbidity and mortality rates in some parts of tropical and subtropical countries. Besides respiratory and metabolic function, lung plays a role in immune system. γδT cells have multiple functions in producing cytokines and chemokines, regulating the immune response by interacting with other cells. It remains unclear about the role of γδT cells in the lung of mice infected by malaria parasites.

METHODS

Flow cytometry (FCM) was used to evaluate the frequency of γδT cells and the effects of γδT cells on the phenotype and function of B and T cells in Plasmodium yoelii-infected wild-type (WT) or γδTCR knockout (γδT KO) mice. Haematoxylin-eosin (HE) staining was used to observe the pathological changes in the lungs.

RESULTS

The percentage and absolute number of γδT cells in the lung increased after Plasmodium infection (p < 0.01). More γδT cells were expressing CD80, CD11b, or PD-1 post-infection (p < 0.05), while less γδT cells were expressing CD34, CD62L, and CD127 post-infection (p < 0.05). The percentages of IL-4, IL-5, IL-6, IL-21, IL-1α, and IL-17 γδT cells were increased (p < 0.05), but the percentage of IFN-γ-expressing γδT cells decreased (p < 0.05) post-infection. The pathological changes in the lungs of the infected γδT KO mice were not obvious compared with the infected WT mice. The proportion of CD3 cells and absolute numbers of CD3 cells, CD3 CD4 cells, CD3 CD8 cells decreased in γδT KO infected mice (p < 0.05). γδT KO infected mice exhibited no significant difference in the surface molecular expression of T cells compared with the WT infected mice (p > 0.05). While, the percentage of IFN-γ-expressing CD3 and CD3 CD8 cells increased in γδT KO infected mice (p < 0.05). There was no significant difference in the absolute numbers of the total, CD69, ICOS, and CD80 B cells between the WT infected and γδT KO infected mice (p > 0.05).

CONCLUSIONS

The content, phenotype, and function of γδT cells in the lung of C57BL/6 mice were changed after Plasmodium infection. γδT cells contribute to T cell immune response in the progress of Plasmodium infection.

摘要

背景

疟疾在一些热带和亚热带国家的发病率和死亡率很高。除了呼吸和代谢功能外,肺在免疫系统中也发挥作用。γδT 细胞在产生细胞因子和趋化因子方面具有多种功能,通过与其他细胞相互作用来调节免疫反应。γδT 细胞在疟原虫感染的小鼠肺部中的作用尚不清楚。

方法

采用流式细胞术(FCM)评估γδT 细胞的频率以及 γδT 细胞对 Plasmodium yoelii 感染的野生型(WT)或 γδTCR 敲除(γδT KO)小鼠中 B 和 T 细胞表型和功能的影响。苏木精-伊红(HE)染色观察肺的病理变化。

结果

疟原虫感染后,肺中γδT 细胞的百分比和绝对数量增加(p<0.01)。感染后,更多的γδT 细胞表达 CD80、CD11b 或 PD-1(p<0.05),而更少的γδT 细胞表达 CD34、CD62L 和 CD127(p<0.05)。IL-4、IL-5、IL-6、IL-21、IL-1α 和 IL-17 γδT 细胞的百分比增加(p<0.05),但 IFN-γ 表达的 γδT 细胞的百分比减少(p<0.05)。与感染 WT 小鼠相比,感染 γδT KO 小鼠的肺部病理变化不明显。γδT KO 感染小鼠的 CD3 细胞比例和 CD3 细胞、CD3 CD4 细胞、CD3 CD8 细胞的绝对数量减少(p<0.05)。与感染 WT 小鼠相比,γδT KO 感染小鼠的 T 细胞表面分子表达没有显著差异(p>0.05)。然而,在感染 γδT KO 的小鼠中,IFN-γ 表达的 CD3 和 CD3 CD8 细胞的百分比增加(p<0.05)。WT 感染和 γδT KO 感染小鼠的总、CD69、ICOS 和 CD80 B 细胞的绝对数量没有显著差异(p>0.05)。

结论

C57BL/6 小鼠感染疟原虫后,肺中 γδT 细胞的含量、表型和功能发生改变。γδT 细胞有助于疟原虫感染过程中的 T 细胞免疫反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2106/7885449/d29dd0e1dff3/12936_2021_3619_Fig1_HTML.jpg

相似文献

1
Characterization of γδT cells in lung of Plasmodium yoelii-infected C57BL/6 mice.
Malar J. 2021 Feb 15;20(1):89. doi: 10.1186/s12936-021-03619-z.
2
Properties and Roles of γδT Cells in NSM Infected C57BL/6 Mice.
Front Cell Infect Microbiol. 2022 Jan 20;11:788546. doi: 10.3389/fcimb.2021.788546. eCollection 2021.
3
Characteristics of splenic PD-1 γδT cells in Plasmodium yoelii nigeriensis infection.
Immunol Res. 2024 Jun;72(3):383-394. doi: 10.1007/s12026-023-09441-w. Epub 2024 Jan 24.
4
Immunological characteristics of CD103CD8 Tc cells in the liver of C57BL/6 mouse infected with plasmodium NSM.
Parasitol Res. 2023 Nov;122(11):2513-2524. doi: 10.1007/s00436-023-07950-z. Epub 2023 Sep 14.
5
Characteristics of γδTCR on myeloid cells from C57BL/6 mice with Plasmodium yoelii nigeriensis infection.
Mol Biochem Parasitol. 2023 Feb;253:111540. doi: 10.1016/j.molbiopara.2022.111540. Epub 2022 Dec 9.
8
[Proportion and characteristics of γδT cells in different tissues and organs of C57BL/6 mice].
Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2013 May;29(5):449-52, 457.
9
Adjustments of γδ T Cells in the Lung of -Infected C56BL/6 Mice.
Front Immunol. 2020 Jun 4;11:1045. doi: 10.3389/fimmu.2020.01045. eCollection 2020.
10
Changes of CD103-expressing pulmonary CD4 and CD8 T cells in S. japonicum infected C57BL/6 mice.
BMC Infect Dis. 2019 Nov 27;19(1):999. doi: 10.1186/s12879-019-4633-8.

引用本文的文献

1
Glycyrrhiza polysaccharides may have an antitumor effect in γδT cells through gut microbiota and TLRs/NF-κB pathway in mice.
FEBS Open Bio. 2024 Jun;14(6):1011-1027. doi: 10.1002/2211-5463.13800. Epub 2024 Apr 11.
2
γδ T cells as immunotherapy for malaria: balancing challenges and opportunities.
Front Immunol. 2023 Dec 6;14:1242306. doi: 10.3389/fimmu.2023.1242306. eCollection 2023.
3
Integrated Network Pharmacology Analysis and Serum Metabolomics to Reveal the Anti-malaria Mechanism of Artesunate.
ACS Omega. 2022 Aug 24;7(35):31482-31494. doi: 10.1021/acsomega.2c04157. eCollection 2022 Sep 6.
4
Experimental Models to Study the Pathogenesis of Malaria-Associated Acute Respiratory Distress Syndrome.
Front Cell Infect Microbiol. 2022 May 23;12:899581. doi: 10.3389/fcimb.2022.899581. eCollection 2022.
5
Properties and Roles of γδT Cells in NSM Infected C57BL/6 Mice.
Front Cell Infect Microbiol. 2022 Jan 20;11:788546. doi: 10.3389/fcimb.2021.788546. eCollection 2021.

本文引用的文献

1
Merozoite surface protein 2 adsorbed onto acetalated dextran microparticles for malaria vaccination.
Int J Pharm. 2021 Jan 25;593:120168. doi: 10.1016/j.ijpharm.2020.120168. Epub 2020 Dec 10.
2
Adjustments of γδ T Cells in the Lung of -Infected C56BL/6 Mice.
Front Immunol. 2020 Jun 4;11:1045. doi: 10.3389/fimmu.2020.01045. eCollection 2020.
3
Lung endothelial cell antigen cross-presentation to CD8T cells drives malaria-associated lung injury.
Nat Commun. 2019 Sep 18;10(1):4241. doi: 10.1038/s41467-019-12017-8.
4
Caspase-11-dependent IL-1α release boosts Th17 immunity against Paracoccidioides brasiliensis.
PLoS Pathog. 2019 Aug 19;15(8):e1007990. doi: 10.1371/journal.ppat.1007990. eCollection 2019 Aug.
6
Human lung tissue resident memory T cells in health and disease.
Curr Opin Immunol. 2019 Aug;59:101-108. doi: 10.1016/j.coi.2019.05.011. Epub 2019 Jun 29.
7
Erythrocyte binding ligand region VI specific IgA confers tissue protection in malaria infection.
Mol Biol Rep. 2019 Aug;46(4):3801-3808. doi: 10.1007/s11033-019-04822-7. Epub 2019 Apr 22.
8
T cell-mediated immunity to malaria.
Nat Rev Immunol. 2019 Jul;19(7):457-471. doi: 10.1038/s41577-019-0158-z.
9
Gamma/Delta T Cells and Their Role in Protection Against Malaria.
Front Immunol. 2018 Dec 20;9:2973. doi: 10.3389/fimmu.2018.02973. eCollection 2018.
10
γδ T cells modulate humoral immunity against Plasmodium berghei infection.
Immunology. 2018 Dec;155(4):519-532. doi: 10.1111/imm.12997. Epub 2018 Sep 24.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验