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Translocation of Viable Gut Microbiota to Mesenteric Adipose Drives Formation of Creeping Fat in Humans
A mysterious feature of Crohn’s disease (CD) is the extra-intestinal manifestation of “creeping fat” (CrF), defined as expansion of mesenteric adipose tissue around the inflamed and fibrotic intestine. In the current study, we explore whether microbial translocation in CD serves as a central cue for...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7521382/ https://www.ncbi.nlm.nih.gov/pubmed/32991841 http://dx.doi.org/10.1016/j.cell.2020.09.009 |
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author | Ha, Connie W.Y. Martin, Anthony Sepich-Poore, Gregory D. Shi, Baochen Wang, Yizhou Gouin, Kenneth Humphrey, Gregory Sanders, Karenina Ratnayake, Yasiru Chan, Kelvin S.L. Hendrick, Gustaf Caldera, J.R. Arias, Christian Moskowitz, Jacob E. Ho Sui, Shannan J. Yang, Shaohong Underhill, David Brady, Matthew J. Knott, Simon Kaihara, Kelly Steinbaugh, Michael J. Li, Huiying McGovern, Dermot P.B. Knight, Rob Fleshner, Phillip Devkota, Suzanne |
author_facet | Ha, Connie W.Y. Martin, Anthony Sepich-Poore, Gregory D. Shi, Baochen Wang, Yizhou Gouin, Kenneth Humphrey, Gregory Sanders, Karenina Ratnayake, Yasiru Chan, Kelvin S.L. Hendrick, Gustaf Caldera, J.R. Arias, Christian Moskowitz, Jacob E. Ho Sui, Shannan J. Yang, Shaohong Underhill, David Brady, Matthew J. Knott, Simon Kaihara, Kelly Steinbaugh, Michael J. Li, Huiying McGovern, Dermot P.B. Knight, Rob Fleshner, Phillip Devkota, Suzanne |
author_sort | Ha, Connie W.Y. |
collection | PubMed |
description | A mysterious feature of Crohn’s disease (CD) is the extra-intestinal manifestation of “creeping fat” (CrF), defined as expansion of mesenteric adipose tissue around the inflamed and fibrotic intestine. In the current study, we explore whether microbial translocation in CD serves as a central cue for CrF development. We discovered a subset of mucosal-associated gut bacteria that consistently translocated and remained viable in CrF in CD ileal surgical resections, and identified Clostridium innocuum as a signature of this consortium with strain variation between mucosal and adipose isolates, suggesting preference for lipid-rich environments. Single-cell RNA sequencing characterized CrF as both pro-fibrotic and pro-adipogenic with a rich milieu of activated immune cells responding to microbial stimuli, which we confirm in gnotobiotic mice colonized with C. innocuum. Ex vivo validation of expression patterns suggests C. innocuum stimulates tissue remodeling via M2 macrophages, leading to an adipose tissue barrier that serves to prevent systemic dissemination of bacteria. |
format | Online Article Text |
id | pubmed-7521382 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75213822020-09-29 Translocation of Viable Gut Microbiota to Mesenteric Adipose Drives Formation of Creeping Fat in Humans Ha, Connie W.Y. Martin, Anthony Sepich-Poore, Gregory D. Shi, Baochen Wang, Yizhou Gouin, Kenneth Humphrey, Gregory Sanders, Karenina Ratnayake, Yasiru Chan, Kelvin S.L. Hendrick, Gustaf Caldera, J.R. Arias, Christian Moskowitz, Jacob E. Ho Sui, Shannan J. Yang, Shaohong Underhill, David Brady, Matthew J. Knott, Simon Kaihara, Kelly Steinbaugh, Michael J. Li, Huiying McGovern, Dermot P.B. Knight, Rob Fleshner, Phillip Devkota, Suzanne Cell Article A mysterious feature of Crohn’s disease (CD) is the extra-intestinal manifestation of “creeping fat” (CrF), defined as expansion of mesenteric adipose tissue around the inflamed and fibrotic intestine. In the current study, we explore whether microbial translocation in CD serves as a central cue for CrF development. We discovered a subset of mucosal-associated gut bacteria that consistently translocated and remained viable in CrF in CD ileal surgical resections, and identified Clostridium innocuum as a signature of this consortium with strain variation between mucosal and adipose isolates, suggesting preference for lipid-rich environments. Single-cell RNA sequencing characterized CrF as both pro-fibrotic and pro-adipogenic with a rich milieu of activated immune cells responding to microbial stimuli, which we confirm in gnotobiotic mice colonized with C. innocuum. Ex vivo validation of expression patterns suggests C. innocuum stimulates tissue remodeling via M2 macrophages, leading to an adipose tissue barrier that serves to prevent systemic dissemination of bacteria. Elsevier Inc. 2020-10-29 2020-09-28 /pmc/articles/PMC7521382/ /pubmed/32991841 http://dx.doi.org/10.1016/j.cell.2020.09.009 Text en © 2020 Elsevier Inc. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Ha, Connie W.Y. Martin, Anthony Sepich-Poore, Gregory D. Shi, Baochen Wang, Yizhou Gouin, Kenneth Humphrey, Gregory Sanders, Karenina Ratnayake, Yasiru Chan, Kelvin S.L. Hendrick, Gustaf Caldera, J.R. Arias, Christian Moskowitz, Jacob E. Ho Sui, Shannan J. Yang, Shaohong Underhill, David Brady, Matthew J. Knott, Simon Kaihara, Kelly Steinbaugh, Michael J. Li, Huiying McGovern, Dermot P.B. Knight, Rob Fleshner, Phillip Devkota, Suzanne Translocation of Viable Gut Microbiota to Mesenteric Adipose Drives Formation of Creeping Fat in Humans |
title | Translocation of Viable Gut Microbiota to Mesenteric Adipose Drives Formation of Creeping Fat in Humans |
title_full | Translocation of Viable Gut Microbiota to Mesenteric Adipose Drives Formation of Creeping Fat in Humans |
title_fullStr | Translocation of Viable Gut Microbiota to Mesenteric Adipose Drives Formation of Creeping Fat in Humans |
title_full_unstemmed | Translocation of Viable Gut Microbiota to Mesenteric Adipose Drives Formation of Creeping Fat in Humans |
title_short | Translocation of Viable Gut Microbiota to Mesenteric Adipose Drives Formation of Creeping Fat in Humans |
title_sort | translocation of viable gut microbiota to mesenteric adipose drives formation of creeping fat in humans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7521382/ https://www.ncbi.nlm.nih.gov/pubmed/32991841 http://dx.doi.org/10.1016/j.cell.2020.09.009 |
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