Cargando…
Lactobacillus paracasei R3 protects against dextran sulfate sodium (DSS)-induced colitis in mice via regulating Th17/Treg cell balance
Inflammatory bowel diseases (IBD), mainly comprising ulcerative colitis (UC) and Crohn's Disease, are most often a polygenic disorder with contributions from the intestinal microbiome, defects in barrier function, and dysregulated host responses to microbial stimulation. Strategies that target...
Autores principales: | , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8371868/ https://www.ncbi.nlm.nih.gov/pubmed/34407839 http://dx.doi.org/10.1186/s12967-021-02943-x |
_version_ | 1783739727583641600 |
---|---|
author | Huang, Juan Yang, Ziyan Li, Yanyun Chai, Xingxing Liang, Yanfang Lin, Bihua Ye, Ziyu Zhang, Shaobing Che, Zhengping Zhang, Hailiang Zhang, Xueying Zhang, Zhao Chen, Tao Yang, Weiqing Zeng, Jincheng |
author_facet | Huang, Juan Yang, Ziyan Li, Yanyun Chai, Xingxing Liang, Yanfang Lin, Bihua Ye, Ziyu Zhang, Shaobing Che, Zhengping Zhang, Hailiang Zhang, Xueying Zhang, Zhao Chen, Tao Yang, Weiqing Zeng, Jincheng |
author_sort | Huang, Juan |
collection | PubMed |
description | Inflammatory bowel diseases (IBD), mainly comprising ulcerative colitis (UC) and Crohn's Disease, are most often a polygenic disorder with contributions from the intestinal microbiome, defects in barrier function, and dysregulated host responses to microbial stimulation. Strategies that target the microbiota have emerged as potential therapies and, of these, probiotics have gained the greatest attention. Herein, we isolated a strain of Lactobacillus paracasei R3 (L.p R3) with strong biofilm formation ability from infant feces. Interestingly, we also found L.p R3 strain can ameliorate the general symptoms of murine colitis, alleviate inflammatory cell infiltration and inhibit Th17 while promote Treg function in murine dextran sulfate sodium (DSS)-induced colitis. Overall, this study suggested that L.p R3 strain significantly improves the symptoms and the pathological damage of mice with colitis and influences the immune function by regulating Th17/Treg cell balance in DSS-induced colitis in mice. |
format | Online Article Text |
id | pubmed-8371868 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-83718682021-08-19 Lactobacillus paracasei R3 protects against dextran sulfate sodium (DSS)-induced colitis in mice via regulating Th17/Treg cell balance Huang, Juan Yang, Ziyan Li, Yanyun Chai, Xingxing Liang, Yanfang Lin, Bihua Ye, Ziyu Zhang, Shaobing Che, Zhengping Zhang, Hailiang Zhang, Xueying Zhang, Zhao Chen, Tao Yang, Weiqing Zeng, Jincheng J Transl Med Research Inflammatory bowel diseases (IBD), mainly comprising ulcerative colitis (UC) and Crohn's Disease, are most often a polygenic disorder with contributions from the intestinal microbiome, defects in barrier function, and dysregulated host responses to microbial stimulation. Strategies that target the microbiota have emerged as potential therapies and, of these, probiotics have gained the greatest attention. Herein, we isolated a strain of Lactobacillus paracasei R3 (L.p R3) with strong biofilm formation ability from infant feces. Interestingly, we also found L.p R3 strain can ameliorate the general symptoms of murine colitis, alleviate inflammatory cell infiltration and inhibit Th17 while promote Treg function in murine dextran sulfate sodium (DSS)-induced colitis. Overall, this study suggested that L.p R3 strain significantly improves the symptoms and the pathological damage of mice with colitis and influences the immune function by regulating Th17/Treg cell balance in DSS-induced colitis in mice. BioMed Central 2021-08-18 /pmc/articles/PMC8371868/ /pubmed/34407839 http://dx.doi.org/10.1186/s12967-021-02943-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Huang, Juan Yang, Ziyan Li, Yanyun Chai, Xingxing Liang, Yanfang Lin, Bihua Ye, Ziyu Zhang, Shaobing Che, Zhengping Zhang, Hailiang Zhang, Xueying Zhang, Zhao Chen, Tao Yang, Weiqing Zeng, Jincheng Lactobacillus paracasei R3 protects against dextran sulfate sodium (DSS)-induced colitis in mice via regulating Th17/Treg cell balance |
title | Lactobacillus paracasei R3 protects against dextran sulfate sodium (DSS)-induced colitis in mice via regulating Th17/Treg cell balance |
title_full | Lactobacillus paracasei R3 protects against dextran sulfate sodium (DSS)-induced colitis in mice via regulating Th17/Treg cell balance |
title_fullStr | Lactobacillus paracasei R3 protects against dextran sulfate sodium (DSS)-induced colitis in mice via regulating Th17/Treg cell balance |
title_full_unstemmed | Lactobacillus paracasei R3 protects against dextran sulfate sodium (DSS)-induced colitis in mice via regulating Th17/Treg cell balance |
title_short | Lactobacillus paracasei R3 protects against dextran sulfate sodium (DSS)-induced colitis in mice via regulating Th17/Treg cell balance |
title_sort | lactobacillus paracasei r3 protects against dextran sulfate sodium (dss)-induced colitis in mice via regulating th17/treg cell balance |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8371868/ https://www.ncbi.nlm.nih.gov/pubmed/34407839 http://dx.doi.org/10.1186/s12967-021-02943-x |
work_keys_str_mv | AT huangjuan lactobacillusparacaseir3protectsagainstdextransulfatesodiumdssinducedcolitisinmiceviaregulatingth17tregcellbalance AT yangziyan lactobacillusparacaseir3protectsagainstdextransulfatesodiumdssinducedcolitisinmiceviaregulatingth17tregcellbalance AT liyanyun lactobacillusparacaseir3protectsagainstdextransulfatesodiumdssinducedcolitisinmiceviaregulatingth17tregcellbalance AT chaixingxing lactobacillusparacaseir3protectsagainstdextransulfatesodiumdssinducedcolitisinmiceviaregulatingth17tregcellbalance AT liangyanfang lactobacillusparacaseir3protectsagainstdextransulfatesodiumdssinducedcolitisinmiceviaregulatingth17tregcellbalance AT linbihua lactobacillusparacaseir3protectsagainstdextransulfatesodiumdssinducedcolitisinmiceviaregulatingth17tregcellbalance AT yeziyu lactobacillusparacaseir3protectsagainstdextransulfatesodiumdssinducedcolitisinmiceviaregulatingth17tregcellbalance AT zhangshaobing lactobacillusparacaseir3protectsagainstdextransulfatesodiumdssinducedcolitisinmiceviaregulatingth17tregcellbalance AT chezhengping lactobacillusparacaseir3protectsagainstdextransulfatesodiumdssinducedcolitisinmiceviaregulatingth17tregcellbalance AT zhanghailiang lactobacillusparacaseir3protectsagainstdextransulfatesodiumdssinducedcolitisinmiceviaregulatingth17tregcellbalance AT zhangxueying lactobacillusparacaseir3protectsagainstdextransulfatesodiumdssinducedcolitisinmiceviaregulatingth17tregcellbalance AT zhangzhao lactobacillusparacaseir3protectsagainstdextransulfatesodiumdssinducedcolitisinmiceviaregulatingth17tregcellbalance AT chentao lactobacillusparacaseir3protectsagainstdextransulfatesodiumdssinducedcolitisinmiceviaregulatingth17tregcellbalance AT yangweiqing lactobacillusparacaseir3protectsagainstdextransulfatesodiumdssinducedcolitisinmiceviaregulatingth17tregcellbalance AT zengjincheng lactobacillusparacaseir3protectsagainstdextransulfatesodiumdssinducedcolitisinmiceviaregulatingth17tregcellbalance |