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基于小鼠肠道共生微生物差异的CD4CD25Foxp3调节性T细胞TCRβ CDR3库的异质性

Heterogeneity of CD4CD25Foxp3Treg TCR β CDR3 Repertoire Based on the Differences of Symbiotic Microorganisms in the Gut of Mice.

作者信息

Li Jun, Xue Huaijuan, Ma Qingqing, He Xiaoyan, Ma Long, Shi Bin, Sun Suhong, Yao Xinsheng

机构信息

Department of Immunology, Center of Immunomolecular Engineering, Innovation & Practice Base for Graduate Students Education, Zunyi Medical University, Zunyi, China.

Department of Laboratory Medicine, Guizhou Aerospace Hospital, Zunyi, China.

出版信息

Front Cell Dev Biol. 2020 Sep 1;8:576445. doi: 10.3389/fcell.2020.576445. eCollection 2020.

Abstract

Gut microbes play a crucial role in the occurrence and development of autoimmune diseases. The diversity of intestinal microorganisms affected by the living environment, regulate the immune function of peripheral immune organs and local tissues. In the study, the diversity of intestinal microorganisms of Germ-free (GF), Specific Pathogen-free (SPF), and Clean (CL) BALB/c mice were conducted by 16S rDNA sequencing. High-throughput sequencing technology was used to analysis the composition and characterization of TCR β chain CDR3 repertoires in Regulatory T cells (Treg) in intestine and spleen of GF, SPF, and CL mice, so as to investigate the effects of differential composition of intestinal microorganisms on the CD4CD25Foxp3Treg TCR β CDR3 repertoire of intestine and spleen. We observed that GF, SPF, and CL mice have different gut microorganism composition, and the abundance and quantity of microorganisms are positively correlated with the level of feeding environment. Interestingly, incomplete structure of spleen and small intestine in GF mice was found. Moreover, a significant difference in the usage of high frequency unique CDR3 amino acid sequences was detected in the intestinal Treg TCRβ CDR3 repertoire among GF, SPF and CL mice, and there were a greater heterogeneity in the usage frequency of , and combinations gene segments. However, the effect of different feeding environment on the mice Treg TCRβ CDR3 repertoire of spleen was weak, implying that the different composition of intestinal microbiota may primarily affect the diversity of the local Treg TCRβ CDR3 repertoire and does not alter the overall properties of the circulating immune system. These results provide basic data to further analyze the mechanism of gut microbes regulating the intestinal mucosal immune system.

摘要

肠道微生物在自身免疫性疾病的发生和发展中起着至关重要的作用。受生活环境影响的肠道微生物多样性,调节外周免疫器官和局部组织的免疫功能。在本研究中,通过16S rDNA测序对无菌(GF)、无特定病原体(SPF)和清洁(CL)BALB/c小鼠的肠道微生物多样性进行了检测。采用高通量测序技术分析GF、SPF和CL小鼠肠道和脾脏中调节性T细胞(Treg)的TCR β链CDR3库的组成和特征,以研究肠道微生物差异组成对肠道和脾脏中CD4CD25Foxp3Treg TCR β CDR3库的影响。我们观察到GF、SPF和CL小鼠具有不同的肠道微生物组成,且微生物的丰度和数量与饲养环境水平呈正相关。有趣的是,发现GF小鼠的脾脏和小肠结构不完整。此外,在GF、SPF和CL小鼠的肠道Treg TCRβ CDR3库中检测到高频独特CDR3氨基酸序列使用上的显著差异,并且 、 和 组合基因片段的使用频率存在更大的异质性。然而,不同饲养环境对小鼠脾脏Treg TCRβ CDR3库的影响较弱,这意味着肠道微生物群的不同组成可能主要影响局部Treg TCRβ CDR3库的多样性,而不会改变循环免疫系统的整体特性。这些结果为进一步分析肠道微生物调节肠道黏膜免疫系统的机制提供了基础数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b92c/7490519/fbdfdbc484f8/fcell-08-576445-g001.jpg

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