Intestinal epithelial Toll-like receptor 4 prevents metabolic syndrome by regulating interactions between microbes and intestinal epithelial cells in mice.

Abstract

Little is known about the pathogenesis of metabolic syndrome, although Toll-like receptor 4 (TLR4) has been implicated. We investigated whether TLR4 in the intestinal epithelium regulates metabolic syndrome by coordinating interactions between the luminal microbiota and host genes that regulate metabolism. Mice lacking TLR4 in the intestinal epithelium (TLR4ΔIEC), but not mice lacking TLR4 in myeloid cells nor mice lacking TLR4 globally, developed metabolic syndrome; these features were not observed in TLR4ΔIEC mice given antibiotics. Metagenomic analysis of the fecal microbiota revealed differences between TLR4ΔIEC and wild-type mice, while meta-transcriptome analysis of the microbiota showed that intestinal TLR4 affected the expression of microbial genes involved in the metabolism of lipids, amino acids, and nucleotides. Genes regulated by peroxisome proliferator-activated receptors (PPARs) and the antimicrobial peptide lysozyme were significantly downregulated in TLR4ΔIEC mice, suggesting a mechanism by which intestinal TLR4 could exert its effects on the microbiota and metabolic syndrome. Supportingly, antibiotics prevented both downregulation of PPAR genes and the development of metabolic syndrome, while PPAR agonists prevented development of metabolic syndrome in TLR4ΔIEC mice. Thus, intestinal epithelial TLR4 regulates metabolic syndrome through altered host-bacterial signaling, suggesting that microbial or PPAR-based strategies might have therapeutic potential for this disease.

• Authors: P Lu, C P Sodhi, Y Yamaguchi, H Jia, T Prindle Jr, W B Fulton, A Vikram, K J Bibby, M J Morowitz, D J Hackam
• Journal: Mucosal immunology (Mucosal Immunol) Vol. 11 Issue 3 Pg. 727-740 (05 2018) ISSN: 1935-3456 [Electronic] United States
• PMID: 29363671 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)

Chemical References

• PPAR gamma
• Tlr4 protein, mouse
• Toll-Like Receptor 4
• Muramidase

Topics

• Animals
• Cells, Cultured
• Host-Pathogen Interactions
• Intestinal Mucosa (microbiology, physiology)
• Metabolic Syndrome (immunology, microbiology)
• Mice
• Mice, Knockout
• Microbiota (immunology)
• Muramidase (metabolism)
• PPAR gamma (genetics, metabolism)
• Signal Transduction
• Toll-Like Receptor 4 (metabolism)