학술논문

Translocation of Viable Gut Microbiota to Mesenteric Adipose Drives Formation of Creeping Fat in Humans.
Document Type
article
Source
Cell. 183(3)
Subject
Mesentery
Ileum
Adipose Tissue
Cells
Cultured
Macrophages
Stem Cells
Animals
Mice
Inbred C57BL
Humans
Mice
Colitis
Ulcerative
Crohn Disease
Lipopolysaccharides
RNA
Ribosomal
16S
Biodiversity
Bacterial Translocation
Germ-Free Life
Cell Polarity
Gene Expression Regulation
Phenotype
Metagenome
Metagenomics
Biomarkers
Gastrointestinal Microbiome
Crohn’s disease
adipogenesis
creeping fat
fibrosis
human microbiome
ileum
inflammatory bowel diseases
macrophages
mesenteric adipose
translocation
Digestive Diseases
Inflammatory Bowel Disease
Crohn's Disease
Prevention
Aetiology
2.1 Biological and endogenous factors
Oral and gastrointestinal
Biological Sciences
Medical and Health Sciences
Developmental Biology
Language
Abstract
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.