Analysis of the Heterogeneity of CD4+CD25+ T Cell TCR β CDR3 Repertoires in Breast Tumor Tissues, Lung Metastatic Tissues, and Spleens from 4T1 Tumor-Bearing BALB/c Mice
To study the homogeneity and heterogeneity of CD4+CD25+ T cells receptor β-chain complementarity determining region 3 (TCR β CDR3) repertoires in breast tumor tissues, lung metastatic tissues, and spleens from 4T1 tumor-bearing BALB/c mice. We used high-throughput sequencing to analyze the character...
Saved in:
Main Authors: | , , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2020-01-01
|
Series: | Journal of Immunology Research |
Online Access: | http://dx.doi.org/10.1155/2020/3184190 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
_version_ | 1832561439224627200 |
---|---|
author | Teng Zhang Fangfang Duan Danhua Su Long Ma Jiezuan Yang Bin Shi Xiaoyan He Rui Ma Suhong Sun Xinsheng Yao |
author_facet | Teng Zhang Fangfang Duan Danhua Su Long Ma Jiezuan Yang Bin Shi Xiaoyan He Rui Ma Suhong Sun Xinsheng Yao |
author_sort | Teng Zhang |
collection | DOAJ |
description | To study the homogeneity and heterogeneity of CD4+CD25+ T cells receptor β-chain complementarity determining region 3 (TCR β CDR3) repertoires in breast tumor tissues, lung metastatic tissues, and spleens from 4T1 tumor-bearing BALB/c mice. We used high-throughput sequencing to analyze the characteristics and changes of CD4+CD25+ TCR β CDR3 repertoires among tumor tissues, lung metastatic tissues, and spleens. The diversity of the CD4+CD25+ TCR β CDR3 repertoires in breast tumor tissue was similar to that of lung metastatic tissues and less pronounced than that of spleen tissues. Breast tumor tissues and lung metastatic tissues had a greater number of high-frequency CDR3 sequences and intermediate-frequency CDR3 sequences than those of spleens. The proportion of unique productive CDR3 sequences in breast tumor tissues and lung metastatic tissues was significantly greater than that in the spleens. The diversity and frequency of the CDR3 repertoires remained homogeneous in breast tumors and lung metastatic tissues and showed great heterogeneity in the spleens, which suggested that the breast tissues and lung metastatic tissues have characteristics of CD4+CD25+ T cells that relate to the tumor microenvironment. However, the number and characteristics of overlapping CDR3 sequences suggested that there were some different CD4+CD25+ T cells in tumors and in the circulatory immune system. The study may be used to further explore the characteristics of the CDR3 repertoires and determine the source of the CD4+CD25+ T cells in the breast cancer microenvironment. |
format | Article |
id | doaj-art-85c17fc0c53d453b8556cd14a6c74065 |
institution | Kabale University |
issn | 2314-8861 2314-7156 |
language | English |
publishDate | 2020-01-01 |
publisher | Wiley |
record_format | Article |
series | Journal of Immunology Research |
spelling | doaj-art-85c17fc0c53d453b8556cd14a6c740652025-02-03T01:24:56ZengWileyJournal of Immunology Research2314-88612314-71562020-01-01202010.1155/2020/31841903184190Analysis of the Heterogeneity of CD4+CD25+ T Cell TCR β CDR3 Repertoires in Breast Tumor Tissues, Lung Metastatic Tissues, and Spleens from 4T1 Tumor-Bearing BALB/c MiceTeng Zhang0Fangfang Duan1Danhua Su2Long Ma3Jiezuan Yang4Bin Shi5Xiaoyan He6Rui Ma7Suhong Sun8Xinsheng Yao9Department of Breast Surgery, The Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, 563000, ChinaDepartment of Immunology, Research Center for Medicine & Biology, Innovation & Practice Base for Graduate Students Education, Zunyi Medical University, Zunyi, Guizhou, 563000, ChinaDepartment of Immunology, Research Center for Medicine & Biology, Innovation & Practice Base for Graduate Students Education, Zunyi Medical University, Zunyi, Guizhou, 563000, ChinaDepartment of Immunology, Research Center for Medicine & Biology, Innovation & Practice Base for Graduate Students Education, Zunyi Medical University, Zunyi, Guizhou, 563000, ChinaDepartment of Infectious Diseases, First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, 310003, ChinaDepartment of Laboratory Medicine, Zunyi Medical University, Zunyi, Guizhou, 563000, ChinaDepartment of Immunology, Research Center for Medicine & Biology, Innovation & Practice Base for Graduate Students Education, Zunyi Medical University, Zunyi, Guizhou, 563000, ChinaDepartment of Immunology, Research Center for Medicine & Biology, Innovation & Practice Base for Graduate Students Education, Zunyi Medical University, Zunyi, Guizhou, 563000, ChinaDepartment of Breast Surgery, The Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, 563000, ChinaDepartment of Immunology, Research Center for Medicine & Biology, Innovation & Practice Base for Graduate Students Education, Zunyi Medical University, Zunyi, Guizhou, 563000, ChinaTo study the homogeneity and heterogeneity of CD4+CD25+ T cells receptor β-chain complementarity determining region 3 (TCR β CDR3) repertoires in breast tumor tissues, lung metastatic tissues, and spleens from 4T1 tumor-bearing BALB/c mice. We used high-throughput sequencing to analyze the characteristics and changes of CD4+CD25+ TCR β CDR3 repertoires among tumor tissues, lung metastatic tissues, and spleens. The diversity of the CD4+CD25+ TCR β CDR3 repertoires in breast tumor tissue was similar to that of lung metastatic tissues and less pronounced than that of spleen tissues. Breast tumor tissues and lung metastatic tissues had a greater number of high-frequency CDR3 sequences and intermediate-frequency CDR3 sequences than those of spleens. The proportion of unique productive CDR3 sequences in breast tumor tissues and lung metastatic tissues was significantly greater than that in the spleens. The diversity and frequency of the CDR3 repertoires remained homogeneous in breast tumors and lung metastatic tissues and showed great heterogeneity in the spleens, which suggested that the breast tissues and lung metastatic tissues have characteristics of CD4+CD25+ T cells that relate to the tumor microenvironment. However, the number and characteristics of overlapping CDR3 sequences suggested that there were some different CD4+CD25+ T cells in tumors and in the circulatory immune system. The study may be used to further explore the characteristics of the CDR3 repertoires and determine the source of the CD4+CD25+ T cells in the breast cancer microenvironment.http://dx.doi.org/10.1155/2020/3184190 |
spellingShingle | Teng Zhang Fangfang Duan Danhua Su Long Ma Jiezuan Yang Bin Shi Xiaoyan He Rui Ma Suhong Sun Xinsheng Yao Analysis of the Heterogeneity of CD4+CD25+ T Cell TCR β CDR3 Repertoires in Breast Tumor Tissues, Lung Metastatic Tissues, and Spleens from 4T1 Tumor-Bearing BALB/c Mice Journal of Immunology Research |
title | Analysis of the Heterogeneity of CD4+CD25+ T Cell TCR β CDR3 Repertoires in Breast Tumor Tissues, Lung Metastatic Tissues, and Spleens from 4T1 Tumor-Bearing BALB/c Mice |
title_full | Analysis of the Heterogeneity of CD4+CD25+ T Cell TCR β CDR3 Repertoires in Breast Tumor Tissues, Lung Metastatic Tissues, and Spleens from 4T1 Tumor-Bearing BALB/c Mice |
title_fullStr | Analysis of the Heterogeneity of CD4+CD25+ T Cell TCR β CDR3 Repertoires in Breast Tumor Tissues, Lung Metastatic Tissues, and Spleens from 4T1 Tumor-Bearing BALB/c Mice |
title_full_unstemmed | Analysis of the Heterogeneity of CD4+CD25+ T Cell TCR β CDR3 Repertoires in Breast Tumor Tissues, Lung Metastatic Tissues, and Spleens from 4T1 Tumor-Bearing BALB/c Mice |
title_short | Analysis of the Heterogeneity of CD4+CD25+ T Cell TCR β CDR3 Repertoires in Breast Tumor Tissues, Lung Metastatic Tissues, and Spleens from 4T1 Tumor-Bearing BALB/c Mice |
title_sort | analysis of the heterogeneity of cd4 cd25 t cell tcr β cdr3 repertoires in breast tumor tissues lung metastatic tissues and spleens from 4t1 tumor bearing balb c mice |
url | http://dx.doi.org/10.1155/2020/3184190 |
work_keys_str_mv | AT tengzhang analysisoftheheterogeneityofcd4cd25tcelltcrbcdr3repertoiresinbreasttumortissueslungmetastatictissuesandspleensfrom4t1tumorbearingbalbcmice AT fangfangduan analysisoftheheterogeneityofcd4cd25tcelltcrbcdr3repertoiresinbreasttumortissueslungmetastatictissuesandspleensfrom4t1tumorbearingbalbcmice AT danhuasu analysisoftheheterogeneityofcd4cd25tcelltcrbcdr3repertoiresinbreasttumortissueslungmetastatictissuesandspleensfrom4t1tumorbearingbalbcmice AT longma analysisoftheheterogeneityofcd4cd25tcelltcrbcdr3repertoiresinbreasttumortissueslungmetastatictissuesandspleensfrom4t1tumorbearingbalbcmice AT jiezuanyang analysisoftheheterogeneityofcd4cd25tcelltcrbcdr3repertoiresinbreasttumortissueslungmetastatictissuesandspleensfrom4t1tumorbearingbalbcmice AT binshi analysisoftheheterogeneityofcd4cd25tcelltcrbcdr3repertoiresinbreasttumortissueslungmetastatictissuesandspleensfrom4t1tumorbearingbalbcmice AT xiaoyanhe analysisoftheheterogeneityofcd4cd25tcelltcrbcdr3repertoiresinbreasttumortissueslungmetastatictissuesandspleensfrom4t1tumorbearingbalbcmice AT ruima analysisoftheheterogeneityofcd4cd25tcelltcrbcdr3repertoiresinbreasttumortissueslungmetastatictissuesandspleensfrom4t1tumorbearingbalbcmice AT suhongsun analysisoftheheterogeneityofcd4cd25tcelltcrbcdr3repertoiresinbreasttumortissueslungmetastatictissuesandspleensfrom4t1tumorbearingbalbcmice AT xinshengyao analysisoftheheterogeneityofcd4cd25tcelltcrbcdr3repertoiresinbreasttumortissueslungmetastatictissuesandspleensfrom4t1tumorbearingbalbcmice |