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Bai and Lipski, 2012) (Table 1)

Experimental evidence indicates that disruption of core clock gene expression affects mitochondrial function, redox balance, and inflammatory signaling, thereby linking circadian dysregulation to metabolic impairment and neuronal vulnerability [14, 15]

coli GI: Gastrointestinal HLA: Human leukocyte antigen HT: Hydroxytryptamine IBD: Inflammatory bowel disease IEC: Intestinal epithelial cell IFN: Interferon IG: Immunoglobulin IL: Interleukin IR: Immune response LAP: Listeria adhesion protein LPS: Lipopolysaccharide LTA: Lipoteichoic acid MAC: Microbiota-associated carbohydrates mTG: Microbial transglutaminase Muc2: Mucin-2 NF-B: Nuclear factor-kappa B NSAIDs: Non-steroidal anti-inflammatory drugs PAD: Peptidylarginine deiminase PAMP: Pathogen-associated molecular pattern PCBs: Polychlorinated biphenyls POPs: Persistent organic pollutant PPI: Proton pump inhibitor RA: Rheumatoid arthritis RF: Rheumatoid factor SCFAs: Short-chain fatty acids SI: Small intestine SLE: Systemic lupus erythematosus Th17: T helper 17 TJ: Tight junction TLR: Toll-like receptor TNF: Tumour necrosis factor tTG: Tissue transglutaminase T1D: Type-1 diabetes ZO: Zonula occludens References Abreu MT (2010) Toll-like receptor signalling in the intestinal epithelium: how bacterial recognition shapes intestinal function