2011
DOI: 10.1074/jbc.m111.271007
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Epigenetic Control of the Host Gene by Commensal Bacteria in Large Intestinal Epithelial Cells

Abstract: Background:Intestinal epithelial cells (IECs) express low levels of TLR4 and are hyporesponsive to commensal bacteria. Results: TLR4 gene is methylated in IECs, and this process is dependent on commensal bacteria in the large intestine. Conclusion: Commensal bacteria control epigenetic modification of the host gene. Significance: This study shows a novel mechanism underlying the maintenance of intestinal symbiosis.

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Cited by 151 publications
(126 citation statements)
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“…Evidence for the involvement of underlying epigenetic modifications in long-term studies emerges with regard to the gastrointestinal tract. More precisely, microbiota is involved in modulating the host epigenome at the gut level [28,29]. Such results, in addition to their well-known prebiotic properties, lead to the idea that scFOS may modulate early bacterial colonization of piglets and by this way modulate metabolic responses later on.…”
Section: Scfos Supplementation Results In Long-term Effects On Growthmentioning
confidence: 99%
“…Evidence for the involvement of underlying epigenetic modifications in long-term studies emerges with regard to the gastrointestinal tract. More precisely, microbiota is involved in modulating the host epigenome at the gut level [28,29]. Such results, in addition to their well-known prebiotic properties, lead to the idea that scFOS may modulate early bacterial colonization of piglets and by this way modulate metabolic responses later on.…”
Section: Scfos Supplementation Results In Long-term Effects On Growthmentioning
confidence: 99%
“…In the intestine, some PRC2 target genes are subject to aberrant DNA methylation following chronic inflammation (Hahn et al 2008). In a noninflammatory context, the LPS-sensing receptor encoding gene TLR4 is down-regulated in intestinal epithelial cells and there is evidence for a role of commensal bacteria in TLR4 methylation (Takahashi et al 2011). This is proposed to maintain intestinal homeostasis by preventing an excessive inflammatory reaction toward the gut microbiota.…”
Section: Dna Methylationmentioning
confidence: 99%
“…Commensal bacteriaderived signals also influence host epigenetic pathways, particularly through DNA and histone methylation [32][33][34][35][36] and histone acetylation and deacetylation [37][38][39][40][41] . The commensal microbiota produces multiple low-molecular-weight byproducts that modify the host cell epigenome and may alter the functional behavior of host cells.…”
Section: Special Issue (Mini Review) Gut Microbiota and Epigeneticsmentioning
confidence: 99%