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Versatility of bacterial outer membrane vesicles in regulating intestinal homeostasis

Outer membrane vesicles (OMVs) play vital roles in bacterial communication both intraspecifically and interspecifically. However, extracellular mechanisms of gut microbiota–derived OMVs in the intestine remain poorly understood. Here, we report that OMVs released from Akkermansia muciniphila are abl...

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Autores principales: Wang, Xinyue, Lin, Sisi, Wang, Lu, Cao, Zhenping, Zhang, Mengmeng, Zhang, Yifan, Liu, Rui, Liu, Jinyao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10017049/
https://www.ncbi.nlm.nih.gov/pubmed/36921043
http://dx.doi.org/10.1126/sciadv.ade5079
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author Wang, Xinyue
Lin, Sisi
Wang, Lu
Cao, Zhenping
Zhang, Mengmeng
Zhang, Yifan
Liu, Rui
Liu, Jinyao
author_facet Wang, Xinyue
Lin, Sisi
Wang, Lu
Cao, Zhenping
Zhang, Mengmeng
Zhang, Yifan
Liu, Rui
Liu, Jinyao
author_sort Wang, Xinyue
collection PubMed
description Outer membrane vesicles (OMVs) play vital roles in bacterial communication both intraspecifically and interspecifically. However, extracellular mechanisms of gut microbiota–derived OMVs in the intestine remain poorly understood. Here, we report that OMVs released from Akkermansia muciniphila are able to (i) restore disturbed balance of the gut microbiota by selectively promoting the proliferation of beneficial bacteria through membrane fusion, (ii) elicit mucosal immunoglobulin A response by translocating into Peyer’s patches and subsequently activating B cells and dendritic cells, and (iii) maintain the integrity of the intestinal barrier by entering intestinal epithelial cells to stimulate the expressions of tight junctions and mucus. We demonstrate that transplantation of gut microbiota–associated OMVs to the intestine can alleviate colitis and enhance anti–programmed cell death protein 1 therapy against colorectal cancer by regulating intestinal homeostasis. This work discloses the importance of gut microbiota–derived OMVs in intestinal ecology, providing an alternative target for disease intervention and treatment.
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spelling pubmed-100170492023-03-16 Versatility of bacterial outer membrane vesicles in regulating intestinal homeostasis Wang, Xinyue Lin, Sisi Wang, Lu Cao, Zhenping Zhang, Mengmeng Zhang, Yifan Liu, Rui Liu, Jinyao Sci Adv Biomedicine and Life Sciences Outer membrane vesicles (OMVs) play vital roles in bacterial communication both intraspecifically and interspecifically. However, extracellular mechanisms of gut microbiota–derived OMVs in the intestine remain poorly understood. Here, we report that OMVs released from Akkermansia muciniphila are able to (i) restore disturbed balance of the gut microbiota by selectively promoting the proliferation of beneficial bacteria through membrane fusion, (ii) elicit mucosal immunoglobulin A response by translocating into Peyer’s patches and subsequently activating B cells and dendritic cells, and (iii) maintain the integrity of the intestinal barrier by entering intestinal epithelial cells to stimulate the expressions of tight junctions and mucus. We demonstrate that transplantation of gut microbiota–associated OMVs to the intestine can alleviate colitis and enhance anti–programmed cell death protein 1 therapy against colorectal cancer by regulating intestinal homeostasis. This work discloses the importance of gut microbiota–derived OMVs in intestinal ecology, providing an alternative target for disease intervention and treatment. American Association for the Advancement of Science 2023-03-15 /pmc/articles/PMC10017049/ /pubmed/36921043 http://dx.doi.org/10.1126/sciadv.ade5079 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Biomedicine and Life Sciences
Wang, Xinyue
Lin, Sisi
Wang, Lu
Cao, Zhenping
Zhang, Mengmeng
Zhang, Yifan
Liu, Rui
Liu, Jinyao
Versatility of bacterial outer membrane vesicles in regulating intestinal homeostasis
title Versatility of bacterial outer membrane vesicles in regulating intestinal homeostasis
title_full Versatility of bacterial outer membrane vesicles in regulating intestinal homeostasis
title_fullStr Versatility of bacterial outer membrane vesicles in regulating intestinal homeostasis
title_full_unstemmed Versatility of bacterial outer membrane vesicles in regulating intestinal homeostasis
title_short Versatility of bacterial outer membrane vesicles in regulating intestinal homeostasis
title_sort versatility of bacterial outer membrane vesicles in regulating intestinal homeostasis
topic Biomedicine and Life Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10017049/
https://www.ncbi.nlm.nih.gov/pubmed/36921043
http://dx.doi.org/10.1126/sciadv.ade5079
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