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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2023
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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. |
format | Online Article Text |
id | pubmed-10017049 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
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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