Cargando…

Mucin degrader Akkermansia muciniphila accelerates intestinal stem cell-mediated epithelial development

Mucin-degrading bacteria are densely populated in the intestinal epithelium; however, their interaction with intestinal stem cells (ISCs) and their progeny have not been elucidated. To determine whether mucin-degrading bacteria play a role in gut homeostasis, mice were treated with Akkermansia mucin...

Descripción completa

Detalles Bibliográficos
Autores principales: Kim, Seungil, Shin, Yun-Chan, Kim, Tae-Young, Kim, Yeji, Lee, Yong-Soo, Lee, Su-Hyun, Kim, Mi-Na, O, Eunju, Kim, Kwang Soon, Kweon, Mi-Na
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7946046/
https://www.ncbi.nlm.nih.gov/pubmed/33678130
http://dx.doi.org/10.1080/19490976.2021.1892441
_version_ 1783662976233897984
author Kim, Seungil
Shin, Yun-Chan
Kim, Tae-Young
Kim, Yeji
Lee, Yong-Soo
Lee, Su-Hyun
Kim, Mi-Na
O, Eunju
Kim, Kwang Soon
Kweon, Mi-Na
author_facet Kim, Seungil
Shin, Yun-Chan
Kim, Tae-Young
Kim, Yeji
Lee, Yong-Soo
Lee, Su-Hyun
Kim, Mi-Na
O, Eunju
Kim, Kwang Soon
Kweon, Mi-Na
author_sort Kim, Seungil
collection PubMed
description Mucin-degrading bacteria are densely populated in the intestinal epithelium; however, their interaction with intestinal stem cells (ISCs) and their progeny have not been elucidated. To determine whether mucin-degrading bacteria play a role in gut homeostasis, mice were treated with Akkermansia muciniphila, a specialized species that degrades mucin. Administration of A. muciniphila for 4 weeks accelerated the proliferation of Lgr5(+) ISCs and promoted the differentiation of Paneth cells and goblet cells in the small intestine (SI). We found similar effects of A. muciniphila in the colon. The levels of acetic and propionic acids were higher in the cecal contents of A. muciniphila-treated mice than in PBS-treated mice. SI organoids treated with cecal contents obtained from A. muciniphila-treated mice were larger and could be diminished by treatment with G protein-coupled receptor (Gpr) 41/43 antagonists. Pre-treatment of mice with A. muciniphila reduced gut damage caused by radiation and methotrexate. Further, a novel isotype of the A. muciniphila strain was isolated from heathy human feces that showed enhanced function in intestinal epithelial regeneration. These findings suggest that mucin-degrading bacteria (e.g., A. muciniphila) may play a crucial role in promoting ISC-mediated epithelial development and contribute to intestinal homeostasis maintenance.
format Online
Article
Text
id pubmed-7946046
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Taylor & Francis
record_format MEDLINE/PubMed
spelling pubmed-79460462021-03-22 Mucin degrader Akkermansia muciniphila accelerates intestinal stem cell-mediated epithelial development Kim, Seungil Shin, Yun-Chan Kim, Tae-Young Kim, Yeji Lee, Yong-Soo Lee, Su-Hyun Kim, Mi-Na O, Eunju Kim, Kwang Soon Kweon, Mi-Na Gut Microbes Research Paper Mucin-degrading bacteria are densely populated in the intestinal epithelium; however, their interaction with intestinal stem cells (ISCs) and their progeny have not been elucidated. To determine whether mucin-degrading bacteria play a role in gut homeostasis, mice were treated with Akkermansia muciniphila, a specialized species that degrades mucin. Administration of A. muciniphila for 4 weeks accelerated the proliferation of Lgr5(+) ISCs and promoted the differentiation of Paneth cells and goblet cells in the small intestine (SI). We found similar effects of A. muciniphila in the colon. The levels of acetic and propionic acids were higher in the cecal contents of A. muciniphila-treated mice than in PBS-treated mice. SI organoids treated with cecal contents obtained from A. muciniphila-treated mice were larger and could be diminished by treatment with G protein-coupled receptor (Gpr) 41/43 antagonists. Pre-treatment of mice with A. muciniphila reduced gut damage caused by radiation and methotrexate. Further, a novel isotype of the A. muciniphila strain was isolated from heathy human feces that showed enhanced function in intestinal epithelial regeneration. These findings suggest that mucin-degrading bacteria (e.g., A. muciniphila) may play a crucial role in promoting ISC-mediated epithelial development and contribute to intestinal homeostasis maintenance. Taylor & Francis 2021-03-08 /pmc/articles/PMC7946046/ /pubmed/33678130 http://dx.doi.org/10.1080/19490976.2021.1892441 Text en © 2021 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Kim, Seungil
Shin, Yun-Chan
Kim, Tae-Young
Kim, Yeji
Lee, Yong-Soo
Lee, Su-Hyun
Kim, Mi-Na
O, Eunju
Kim, Kwang Soon
Kweon, Mi-Na
Mucin degrader Akkermansia muciniphila accelerates intestinal stem cell-mediated epithelial development
title Mucin degrader Akkermansia muciniphila accelerates intestinal stem cell-mediated epithelial development
title_full Mucin degrader Akkermansia muciniphila accelerates intestinal stem cell-mediated epithelial development
title_fullStr Mucin degrader Akkermansia muciniphila accelerates intestinal stem cell-mediated epithelial development
title_full_unstemmed Mucin degrader Akkermansia muciniphila accelerates intestinal stem cell-mediated epithelial development
title_short Mucin degrader Akkermansia muciniphila accelerates intestinal stem cell-mediated epithelial development
title_sort mucin degrader akkermansia muciniphila accelerates intestinal stem cell-mediated epithelial development
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7946046/
https://www.ncbi.nlm.nih.gov/pubmed/33678130
http://dx.doi.org/10.1080/19490976.2021.1892441
work_keys_str_mv AT kimseungil mucindegraderakkermansiamuciniphilaacceleratesintestinalstemcellmediatedepithelialdevelopment
AT shinyunchan mucindegraderakkermansiamuciniphilaacceleratesintestinalstemcellmediatedepithelialdevelopment
AT kimtaeyoung mucindegraderakkermansiamuciniphilaacceleratesintestinalstemcellmediatedepithelialdevelopment
AT kimyeji mucindegraderakkermansiamuciniphilaacceleratesintestinalstemcellmediatedepithelialdevelopment
AT leeyongsoo mucindegraderakkermansiamuciniphilaacceleratesintestinalstemcellmediatedepithelialdevelopment
AT leesuhyun mucindegraderakkermansiamuciniphilaacceleratesintestinalstemcellmediatedepithelialdevelopment
AT kimmina mucindegraderakkermansiamuciniphilaacceleratesintestinalstemcellmediatedepithelialdevelopment
AT oeunju mucindegraderakkermansiamuciniphilaacceleratesintestinalstemcellmediatedepithelialdevelopment
AT kimkwangsoon mucindegraderakkermansiamuciniphilaacceleratesintestinalstemcellmediatedepithelialdevelopment
AT kweonmina mucindegraderakkermansiamuciniphilaacceleratesintestinalstemcellmediatedepithelialdevelopment