Cargando…

Lactobacillus murinus alleviate intestinal ischemia/reperfusion injury through promoting the release of interleukin-10 from M2 macrophages via Toll-like receptor 2 signaling

BACKGROUND: Intestinal ischemia/reperfusion (I/R) injury has high morbidity and mortality rates. Gut microbiota is a potential key factor affecting intestinal I/R injury. Populations exhibit different sensitivities to intestinal I/R injury; however, whether this interpopulation difference is related...

Descripción completa

Detalles Bibliográficos
Autores principales: Hu, Jingjuan, Deng, Fan, Zhao, Bingcheng, Lin, Zebin, Sun, Qishun, Yang, Xiao, Wu, Mei, Qiu, Shida, Chen, Yu, Yan, Zhengzheng, Luo, Sidan, Zhao, Jin, Liu, Weifeng, Li, Cai, Liu, Ke Xuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8896269/
https://www.ncbi.nlm.nih.gov/pubmed/35241180
http://dx.doi.org/10.1186/s40168-022-01227-w
_version_ 1784663124988657664
author Hu, Jingjuan
Deng, Fan
Zhao, Bingcheng
Lin, Zebin
Sun, Qishun
Yang, Xiao
Wu, Mei
Qiu, Shida
Chen, Yu
Yan, Zhengzheng
Luo, Sidan
Zhao, Jin
Liu, Weifeng
Li, Cai
Liu, Ke Xuan
author_facet Hu, Jingjuan
Deng, Fan
Zhao, Bingcheng
Lin, Zebin
Sun, Qishun
Yang, Xiao
Wu, Mei
Qiu, Shida
Chen, Yu
Yan, Zhengzheng
Luo, Sidan
Zhao, Jin
Liu, Weifeng
Li, Cai
Liu, Ke Xuan
author_sort Hu, Jingjuan
collection PubMed
description BACKGROUND: Intestinal ischemia/reperfusion (I/R) injury has high morbidity and mortality rates. Gut microbiota is a potential key factor affecting intestinal I/R injury. Populations exhibit different sensitivities to intestinal I/R injury; however, whether this interpopulation difference is related to variation in gut microbiota is unclear. Here, to elucidate the interaction between the gut microbiome and intestinal I/R injury, we performed 16S DNA sequencing on the preoperative feces of C57BL/6 mice and fecal microbiota transplantation (FMT) experiments in germ-free mice. The transwell co-culture system of small intestinal organoids extracted from control mice and macrophages extracted from control mice or Toll-like receptor 2 (TLR2)-deficient mice or interleukin-10 (IL-10)-deficient mice were established separately to explore the potential mechanism of reducing intestinal I/R injury. RESULTS: Intestinal I/R-sensitive (Sen) and intestinal I/R-resistant (Res) mice were first defined according to different survival outcomes of mice suffering from intestinal I/R. Fecal microbiota composition and diversity prior to intestinal ischemia differed between Sen and Res mice. The relative abundance of Lactobacillus murinus (L. murinus) at the species level was drastically higher in Res than that in Sen mice. Clinically, the abundance of L. murinus in preoperative feces of patients undergoing cardiopulmonary bypass surgery was closely related to the degree of intestinal I/R injury after surgery. Treatment with L. murinus significantly prevented intestinal I/R-induced intestinal injury and improved mouse survival, which depended on macrophages involvement. Further, in vitro experiments indicated that promoting the release of IL-10 from macrophages through TLR2 may be a potential mechanism for L. murinus to reduce intestinal I/R injury. CONCLUSION: The gut microbiome is involved in the postoperative outcome of intestinal I/R. Lactobacillus murinus alleviates mice intestinal I/R injury through macrophages, and promoting the release of IL-10 from macrophages through TLR2 may be a potential mechanism for L. murinus to reduce intestinal I/R injury. This study revealed a novel mechanism of intestinal I/R injury and a new therapeutic strategy for clinical practice. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-022-01227-w.
format Online
Article
Text
id pubmed-8896269
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-88962692022-03-14 Lactobacillus murinus alleviate intestinal ischemia/reperfusion injury through promoting the release of interleukin-10 from M2 macrophages via Toll-like receptor 2 signaling Hu, Jingjuan Deng, Fan Zhao, Bingcheng Lin, Zebin Sun, Qishun Yang, Xiao Wu, Mei Qiu, Shida Chen, Yu Yan, Zhengzheng Luo, Sidan Zhao, Jin Liu, Weifeng Li, Cai Liu, Ke Xuan Microbiome Research BACKGROUND: Intestinal ischemia/reperfusion (I/R) injury has high morbidity and mortality rates. Gut microbiota is a potential key factor affecting intestinal I/R injury. Populations exhibit different sensitivities to intestinal I/R injury; however, whether this interpopulation difference is related to variation in gut microbiota is unclear. Here, to elucidate the interaction between the gut microbiome and intestinal I/R injury, we performed 16S DNA sequencing on the preoperative feces of C57BL/6 mice and fecal microbiota transplantation (FMT) experiments in germ-free mice. The transwell co-culture system of small intestinal organoids extracted from control mice and macrophages extracted from control mice or Toll-like receptor 2 (TLR2)-deficient mice or interleukin-10 (IL-10)-deficient mice were established separately to explore the potential mechanism of reducing intestinal I/R injury. RESULTS: Intestinal I/R-sensitive (Sen) and intestinal I/R-resistant (Res) mice were first defined according to different survival outcomes of mice suffering from intestinal I/R. Fecal microbiota composition and diversity prior to intestinal ischemia differed between Sen and Res mice. The relative abundance of Lactobacillus murinus (L. murinus) at the species level was drastically higher in Res than that in Sen mice. Clinically, the abundance of L. murinus in preoperative feces of patients undergoing cardiopulmonary bypass surgery was closely related to the degree of intestinal I/R injury after surgery. Treatment with L. murinus significantly prevented intestinal I/R-induced intestinal injury and improved mouse survival, which depended on macrophages involvement. Further, in vitro experiments indicated that promoting the release of IL-10 from macrophages through TLR2 may be a potential mechanism for L. murinus to reduce intestinal I/R injury. CONCLUSION: The gut microbiome is involved in the postoperative outcome of intestinal I/R. Lactobacillus murinus alleviates mice intestinal I/R injury through macrophages, and promoting the release of IL-10 from macrophages through TLR2 may be a potential mechanism for L. murinus to reduce intestinal I/R injury. This study revealed a novel mechanism of intestinal I/R injury and a new therapeutic strategy for clinical practice. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-022-01227-w. BioMed Central 2022-03-03 /pmc/articles/PMC8896269/ /pubmed/35241180 http://dx.doi.org/10.1186/s40168-022-01227-w Text en © The Author(s) 2022 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
Hu, Jingjuan
Deng, Fan
Zhao, Bingcheng
Lin, Zebin
Sun, Qishun
Yang, Xiao
Wu, Mei
Qiu, Shida
Chen, Yu
Yan, Zhengzheng
Luo, Sidan
Zhao, Jin
Liu, Weifeng
Li, Cai
Liu, Ke Xuan
Lactobacillus murinus alleviate intestinal ischemia/reperfusion injury through promoting the release of interleukin-10 from M2 macrophages via Toll-like receptor 2 signaling
title Lactobacillus murinus alleviate intestinal ischemia/reperfusion injury through promoting the release of interleukin-10 from M2 macrophages via Toll-like receptor 2 signaling
title_full Lactobacillus murinus alleviate intestinal ischemia/reperfusion injury through promoting the release of interleukin-10 from M2 macrophages via Toll-like receptor 2 signaling
title_fullStr Lactobacillus murinus alleviate intestinal ischemia/reperfusion injury through promoting the release of interleukin-10 from M2 macrophages via Toll-like receptor 2 signaling
title_full_unstemmed Lactobacillus murinus alleviate intestinal ischemia/reperfusion injury through promoting the release of interleukin-10 from M2 macrophages via Toll-like receptor 2 signaling
title_short Lactobacillus murinus alleviate intestinal ischemia/reperfusion injury through promoting the release of interleukin-10 from M2 macrophages via Toll-like receptor 2 signaling
title_sort lactobacillus murinus alleviate intestinal ischemia/reperfusion injury through promoting the release of interleukin-10 from m2 macrophages via toll-like receptor 2 signaling
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8896269/
https://www.ncbi.nlm.nih.gov/pubmed/35241180
http://dx.doi.org/10.1186/s40168-022-01227-w
work_keys_str_mv AT hujingjuan lactobacillusmurinusalleviateintestinalischemiareperfusioninjurythroughpromotingthereleaseofinterleukin10fromm2macrophagesviatolllikereceptor2signaling
AT dengfan lactobacillusmurinusalleviateintestinalischemiareperfusioninjurythroughpromotingthereleaseofinterleukin10fromm2macrophagesviatolllikereceptor2signaling
AT zhaobingcheng lactobacillusmurinusalleviateintestinalischemiareperfusioninjurythroughpromotingthereleaseofinterleukin10fromm2macrophagesviatolllikereceptor2signaling
AT linzebin lactobacillusmurinusalleviateintestinalischemiareperfusioninjurythroughpromotingthereleaseofinterleukin10fromm2macrophagesviatolllikereceptor2signaling
AT sunqishun lactobacillusmurinusalleviateintestinalischemiareperfusioninjurythroughpromotingthereleaseofinterleukin10fromm2macrophagesviatolllikereceptor2signaling
AT yangxiao lactobacillusmurinusalleviateintestinalischemiareperfusioninjurythroughpromotingthereleaseofinterleukin10fromm2macrophagesviatolllikereceptor2signaling
AT wumei lactobacillusmurinusalleviateintestinalischemiareperfusioninjurythroughpromotingthereleaseofinterleukin10fromm2macrophagesviatolllikereceptor2signaling
AT qiushida lactobacillusmurinusalleviateintestinalischemiareperfusioninjurythroughpromotingthereleaseofinterleukin10fromm2macrophagesviatolllikereceptor2signaling
AT chenyu lactobacillusmurinusalleviateintestinalischemiareperfusioninjurythroughpromotingthereleaseofinterleukin10fromm2macrophagesviatolllikereceptor2signaling
AT yanzhengzheng lactobacillusmurinusalleviateintestinalischemiareperfusioninjurythroughpromotingthereleaseofinterleukin10fromm2macrophagesviatolllikereceptor2signaling
AT luosidan lactobacillusmurinusalleviateintestinalischemiareperfusioninjurythroughpromotingthereleaseofinterleukin10fromm2macrophagesviatolllikereceptor2signaling
AT zhaojin lactobacillusmurinusalleviateintestinalischemiareperfusioninjurythroughpromotingthereleaseofinterleukin10fromm2macrophagesviatolllikereceptor2signaling
AT liuweifeng lactobacillusmurinusalleviateintestinalischemiareperfusioninjurythroughpromotingthereleaseofinterleukin10fromm2macrophagesviatolllikereceptor2signaling
AT licai lactobacillusmurinusalleviateintestinalischemiareperfusioninjurythroughpromotingthereleaseofinterleukin10fromm2macrophagesviatolllikereceptor2signaling
AT liukexuan lactobacillusmurinusalleviateintestinalischemiareperfusioninjurythroughpromotingthereleaseofinterleukin10fromm2macrophagesviatolllikereceptor2signaling