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Bacteroides thetaiotaomicron and Faecalibacterium prausnitzii influence the production of mucus glycans and the development of goblet cells in the colonic epithelium of a gnotobiotic model rodent
- Source :
- BMC Biology, BMC Biology, BioMed Central, 2013, 11, online (may), Non paginé. ⟨10.1186/1741-7007-11-61⟩, BMC Biology, 2013, 11, online (may), Non paginé. ⟨10.1186/1741-7007-11-61⟩, BMC Biology, BioMed Central, 2013, 11, online (may), Non paginé. 〈10.1186/1741-7007-11-61〉, BMC Biology may (11, online), Non paginé. (2013)
- Publication Year :
- 2013
- Publisher :
- HAL CCSD, 2013.
-
Abstract
- Background The intestinal mucus layer plays a key role in the maintenance of host-microbiota homeostasis. To document the crosstalk between the host and microbiota, we used gnotobiotic models to study the influence of two major commensal bacteria, Bacteroides thetaiotaomicron and Faecalibacterium prausnitzii, on this intestinal mucus layer. B. thetaiotaomicron is known to use polysaccharides from mucus, but its effect on goblet cells has not been addressed so far. F. prausnitzii is of particular physiological importance because it can be considered as a sensor and a marker of human health. We determined whether B. thetaiotaomicron affected goblet cell differentiation, mucin synthesis and glycosylation in the colonic epithelium. We then investigated how F. prausnitzii influenced the colonic epithelial responses to B. thetaiotaomicron. Results B. thetaiotaomicron, an acetate producer, increased goblet cell differentiation, expression of mucus-related genes and the ratio of sialylated to sulfated mucins in mono-associated rats. B. thetaiotaomicron, therefore, stimulates the secretory lineage, favoring mucus production. When B. thetaiotaomicron was associated with F. prausnitzii, an acetate consumer and a butyrate producer, the effects on goblet cells and mucin glycosylation were diminished. F. prausnitzii, by attenuating the effects of B. thetaiotaomicron on mucus, may help the epithelium to maintain appropriate proportions of different cell types of the secretory lineage. Using a mucus-producing cell line, we showed that acetate up-regulated KLF4, a transcription factor involved in goblet cell differentiation. Conclusions B. thetaiotaomicron and F. prausnitzii, which are metabolically complementary, modulate, in vivo, the intestinal mucus barrier by modifying goblet cells and mucin glycosylation. Our study reveals the importance of the balance between two main commensal bacteria in maintaining colonic epithelial homeostasis via their respective effects on mucus.
- Subjects :
- [SDV.SA]Life Sciences [q-bio]/Agricultural sciences
Glycosylation
Time Factors
Physiology
Faecalibacterium prausnitzii
Plant Science
Acetates
Germ-free rats
0302 clinical medicine
fluids and secretions
Intestinal mucosa
Structural Biology
Ruminococcus
Bacteroides
Intestinal Mucosa
[ SDV.SA ] Life Sciences [q-bio]/Agricultural sciences
Goblet cells
0303 health sciences
biology
Agricultural and Biological Sciences(all)
goblet cell
Cell Differentiation
Germ-free rat
Goblet cell
klf4
Short chain fatty acid
mucin o-glycosylation
respiratory system
Bacteroides Infections
medicine.anatomical_structure
Host-Pathogen Interactions
030211 gastroenterology & hepatology
General Agricultural and Biological Sciences
Bacteroides thetaiotaomicron
HT29 Cells
Biotechnology
Signal Transduction
Research Article
Colon
short chain fatty acid
digestive system
General Biochemistry, Genetics and Molecular Biology
Microbiology
germ-free rat
03 medical and health sciences
Kruppel-Like Factor 4
Polysaccharides
medicine
Animals
Germ-Free Life
Humans
Ecology, Evolution, Behavior and Systematics
Gram-Positive Bacterial Infections
030304 developmental biology
Biochemistry, Genetics and Molecular Biology(all)
Mucin
Cell Biology
biology.organism_classification
Mucus
Rats
carbohydrates (lipids)
Disease Models, Animal
Gene Expression Regulation
Developmental Biology
Subjects
Details
- Language :
- English
- ISSN :
- 17417007
- Database :
- OpenAIRE
- Journal :
- BMC Biology, BMC Biology, BioMed Central, 2013, 11, online (may), Non paginé. ⟨10.1186/1741-7007-11-61⟩, BMC Biology, 2013, 11, online (may), Non paginé. ⟨10.1186/1741-7007-11-61⟩, BMC Biology, BioMed Central, 2013, 11, online (may), Non paginé. 〈10.1186/1741-7007-11-61〉, BMC Biology may (11, online), Non paginé. (2013)
- Accession number :
- edsair.doi.dedup.....d051210e4c5b93c26492c3930f1d556a
- Full Text :
- https://doi.org/10.1186/1741-7007-11-61⟩