Butyrate enhances the intestinal barrier by facilitating tight junction assembly via activation of AMP-activated protein kinase in Caco-2 cell monolayers.

Butyrate, one of the SCFA, promotes the development of the intestinal barrier. However, the molecular mechanisms underlying the butyrate regulation of the intestinal barrier are unknown. To test the hypothesis that the effect of butyrate on the intestinal barrier is mediated by the regulation of the assembly of tight junctions involving the activation of the AMP-activated protein kinase (AMPK), we determined the effect of butyrate on the intestinal barrier by measuring the transepithelial electrical resistance (TER) and inulin permeability in a Caco-2 cell monolayer model. We further used a calcium switch assay to study the assembly of epithelial tight junctions and determined the effect of butyrate on the assembly of epithelial tight junctions and AMPK activity. We demonstrated that the butyrate treatment increased AMPK activity and accelerated the assembly of tight junctions as shown by the reorganization of tight junction proteins, as well as the development of TER. AMPK activity was also upregulated by butyrate during calcium switch-induced tight junction assembly. Compound C, a specific AMPK inhibitor, inhibited the butyrate-induced activation of AMPK. The facilitating effect of butyrate on the increases in TER in standard culture media, as well as after calcium switch, was abolished by compound C. We conclude that butyrate enhances the intestinal barrier by regulating the assembly of tight junctions. This dynamic process is mediated by the activation of AMPK. These results suggest an intriguing link between SCFA and the intracellular energy sensor for the development of the intestinal barrier.

[1]  Takuya Suzuki,et al.  Phosphorylation of Tyr-398 and Tyr-402 in Occludin Prevents Its Interaction with ZO-1 and Destabilizes Its Assembly at the Tight Junctions* , 2009, Journal of Biological Chemistry.

[2]  James M. Anderson,et al.  The Tight Junction Protein ZO-1 Establishes a Link between the Transmembrane Protein Occludin and the Actin Cytoskeleton* , 1998, The Journal of Biological Chemistry.

[3]  D. Roberts,et al.  Development and differentiation of the intestinal epithelium , 2003, Cellular and Molecular Life Sciences CMLS.

[4]  D. Hardie,et al.  Regulation of fatty acid synthesis and oxidation by the AMP-activated protein kinase. , 2001, Biochemical Society transactions.

[5]  D. Hardie,et al.  AMP-activated protein kinase: ancient energy gauge provides clues to modern understanding of metabolism. , 2005, Cell metabolism.

[6]  N. Ruderman,et al.  AMP-activated Protein Kinase Is Activated as a Consequence of Lipolysis in the Adipocyte , 2008, Journal of Biological Chemistry.

[7]  C. V. Van Itallie,et al.  Tight junctions and the molecular basis for regulation of paracellular permeability. , 1995, The American journal of physiology.

[8]  T. Kadowaki,et al.  Acetic acid activates hepatic AMPK and reduces hyperglycemia in diabetic KK-A(y) mice. , 2006, Biochemical and biophysical research communications.

[9]  M. Caplan,et al.  AMP-activated protein kinase regulates the assembly of epithelial tight junctions , 2006, Proceedings of the National Academy of Sciences.

[10]  C. L. Kien,et al.  Quantitation of Colonic Luminal Synthesis of Butyric Acid in Piglets , 2002, Journal of pediatric gastroenterology and nutrition.

[11]  S. Krishnan,et al.  Stimulation of Sodium Chloride Absorption from Secreting Rat Colon by Short-Chain Fatty Acids , 1999, Digestive Diseases and Sciences.

[12]  W. Walker,et al.  Development of Gastrointestinal Mucosal Barrier. II. The Effect of Natural Versus Artificial Feeding on Intestinal Permeability to Macromolecules , 1981, Pediatric Research.

[13]  D. Hardie,et al.  5-aminoimidazole-4-carboxamide ribonucleoside. A specific method for activating AMP-activated protein kinase in intact cells? , 1995, European journal of biochemistry.

[14]  Takuya Suzuki,et al.  Physiological concentrations of short-chain fatty acids immediately suppress colonic epithelial permeability , 2008, British Journal of Nutrition.

[15]  Margaret S. Wu,et al.  Role of AMP-activated protein kinase in mechanism of metformin action. , 2001, The Journal of clinical investigation.

[16]  Luying Peng,et al.  Effects of Butyrate on Intestinal Barrier Function in a Caco-2 Cell Monolayer Model of Intestinal Barrier , 2007, Pediatric Research.

[17]  J. Turner,et al.  Stimulus-induced reorganization of tight junction structure: the role of membrane traffic. , 2008, Biochimica et biophysica acta.

[18]  H. Yamashita,et al.  Mechanism for Fatty Acid “Sparing” Effect on Glucose-induced Transcription , 2002, The Journal of Biological Chemistry.

[19]  J. Bond,et al.  Fate of soluble carbohydrate in the colon of rats and man. , 1976, The Journal of clinical investigation.

[20]  S. Hawley,et al.  5-aminoimidazole-4-carboxamide ribonucleoside. A specific method for activating AMP-activated protein kinase in intact cells? , 1995, European journal of biochemistry.

[21]  C. V. Van Itallie,et al.  Setting up a selective barrier at the apical junction complex. , 2004, Current opinion in cell biology.

[22]  J. Mariadason,et al.  Effect of short-chain fatty acids on paracellular permeability in Caco-2 intestinal epithelium model. , 1997, The American journal of physiology.

[23]  A. Means,et al.  The Ca2+/Calmodulin-dependent Protein Kinase Kinases Are AMP-activated Protein Kinase Kinases* , 2005, Journal of Biological Chemistry.

[24]  J. Macfie Enteral versus parenteral nutrition: the significance of bacterial translocation and gut-barrier function. , 2000, Nutrition.

[25]  D. Samuelson,et al.  Glutamine regulates Caco-2 cell tight junction proteins. , 2004, American journal of physiology. Gastrointestinal and liver physiology.

[26]  W. Walker,et al.  Development of Gastrointestinal Mucosal Barrier. I. The Effect of Age on Intestinal Permeability to Macromolecules , 1981, Pediatric Research.

[27]  W. Walker Development of the Intestinal Mucosal Barrier , 2002, Journal of pediatric gastroenterology and nutrition.

[28]  T. Sakata Stimulatory effect of short-chain fatty acids on epithelial cell proliferation in the rat intestine: a possible explanation for trophic effects of fermentable fibre, gut microbes and luminal trophic factors , 1987, British Journal of Nutrition.

[29]  R. Rao,et al.  Expression of Kinase-inactive c-Src Delays Oxidative Stress-induced Disassembly and Accelerates Calcium-mediated Reassembly of Tight Junctions in the Caco-2 Cell Monolayer* , 2003, The Journal of Biological Chemistry.

[30]  G. Ramsay,et al.  Intestinal Permeability and Carrier-Mediated Monosaccharide Absorption in Preterm Neonates during the Early Postnatal Period , 2002, Pediatric Research.

[31]  D. Hardie The AMP-activated protein kinase pathway – new players upstream and downstream , 2004, Journal of Cell Science.

[32]  L. Cantley,et al.  Regulation of epithelial tight junction assembly and disassembly by AMP-activated protein kinase , 2007, Proceedings of the National Academy of Sciences.

[33]  D. Hardie,et al.  AMP‐activated protein kinase – development of the energy sensor concept , 2006, The Journal of physiology.

[34]  R. Heath,et al.  Ca2+/calmodulin-dependent protein kinase kinase-beta acts upstream of AMP-activated protein kinase in mammalian cells. , 2005, Cell metabolism.

[35]  A. Edelman,et al.  Calmodulin-dependent protein kinase kinase-beta is an alternative upstream kinase for AMP-activated protein kinase. , 2005, Cell metabolism.

[36]  Takuya Suzuki,et al.  PKCη regulates occludin phosphorylation and epithelial tight junction integrity , 2009, Proceedings of the National Academy of Sciences.

[37]  J. Mariadason,et al.  Modulation of distal colonic epithelial barrier function by dietary fibre in normal rats , 1999, Gut.

[38]  W. Roediger Utilization of nutrients by isolated epithelial cells of the rat colon. , 1982, Gastroenterology.

[39]  R. Harvey,et al.  Necrotizing Enterocolitis in Preterm Pigs Diet-Dependent Effects of Minimal Enteral Nutrition , 2003 .

[40]  C. V. Van Itallie,et al.  Molecular physiology and pathophysiology of tight junctions I. Tight junction structure and function: lessons from mutant animals and proteins. , 2000, American journal of physiology. Gastrointestinal and liver physiology.

[41]  D. Hardie,et al.  AMP‐activated protein kinase: the energy charge hypothesis revisited , 2001, BioEssays : news and reviews in molecular, cellular and developmental biology.

[42]  M. Krempf,et al.  Production rates and metabolism of short-chain fatty acids in the colon and whole body using stable isotopes. , 2003, The Proceedings of the Nutrition Society.

[43]  J. Rombeau,et al.  Parenteral nutrition supplemented with short-chain fatty acids: effect on the small-bowel mucosa in normal rats. , 1990, The American journal of clinical nutrition.

[44]  B. Kemp,et al.  Functional Domains of the α1 Catalytic Subunit of the AMP-activated Protein Kinase* , 1998, The Journal of Biological Chemistry.

[45]  I. Sanderson Short chain fatty acid regulation of signaling genes expressed by the intestinal epithelium. , 2004, The Journal of nutrition.

[46]  C. Cherbut,et al.  Neonatal antibiotic treatment alters gastrointestinal tract developmental gene expression and intestinal barrier transcriptome. , 2005, Physiological genomics.