The gastrointestinal tract consists of an enormous surface area that is optimized to efficiently absorb nutrients, water, and electrolytes from food. At the same time, it needs to provide a tight barrier against the ingress of harmful substances, and protect against a reaction to omnipresent harmless compounds. A dysfunctional intestinal barrier is associated with various diseases and disorders. In this review, the role of intestinal permeability in common disorders such as infections with intestinal pathogens, inflammatory bowel disease, irritable bowel syndrome, obesity, celiac disease, non-celiac gluten sensitivity, and food allergies will be discussed. In addition, the effect of the frequently prescribed drugs proton pump inhibitors and non-steroidal anti-inflammatory drugs on intestinal permeability, as well as commonly used methods to assess barrier function will be reviewed.
Bischoff Stephan C, Barbara Giovanni, Buurman Wim, Ockhuizen Theo, Schulzke Jörg-Dieter, Serino Matteo, Tilg Herbert, Watson Alastair, Wells Jerry M, Intestinal permeability – a new target for disease prevention and therapy, 10.1186/s12876-014-0189-7
Dörfel M, Biomed Res Int, 2012, 807356 (2012)
Dörfel Max J., Huber Otmar, A phosphorylation hotspot within the occludin C-terminal domain : Occludin phosphorylation hotspot, 10.1111/j.1749-6632.2012.06536.x
Petecchia Loredana, Sabatini Federica, Usai Cesare, Caci Emanuela, Varesio Luigi, Rossi Giovanni A, Cytokines induce tight junction disassembly in airway cells via an EGFR-dependent MAPK/ERK1/2-pathway, 10.1038/labinvest.2012.67
Al-Sadi Rana, Guo Shuhong, Ye Dongmei, Ma Thomas Y., TNF-α Modulation of Intestinal Epithelial Tight Junction Barrier Is Regulated by ERK1/2 Activation of Elk-1, 10.1016/j.ajpath.2013.09.001
Al-Sadi R., Guo S., Ye D., Dokladny K., Alhmoud T., Ereifej L., Said H. M., Ma T. Y., Mechanism of IL-1 Modulation of Intestinal Epithelial Barrier Involves p38 Kinase and Activating Transcription Factor-2 Activation, 10.4049/jimmunol.1201876
Zheng Bin, Cantley Lewis C., Regulation of epithelial tight junction assembly and disassembly by AMP-activated protein kinase, 10.1073/pnas.0610157104
Ye J, Am J Physiol Physiol, 277, F524 (1999)
Rao Radhakrishna, Oxidative stress-induced disruption of epithelial and endothelial tight junctions, 10.2741/3223
Turner JR, Am J Physiol Physiol, 273, C1378 (1997)
Lapointe Tamia K, O'Connor Pamela M, Buret Andre G, The role of epithelial malfunction in the pathogenesis of enteropathogenic E. coli-induced diarrhea, 10.1038/labinvest.2009.69
Frankel Gad, Phillips Alan D., Attaching effacing Escherichia coli and paradigms of Tir-triggered actin polymerization: getting off the pedestal, 10.1111/j.1462-5822.2007.01103.x
Muza-Moons Michelle M., Schneeberger Eveline E., Hecht Gail A., Enteropathogenic Escherichia coli infection leads to appearance of aberrant tight junctions strands in the lateral membrane of intestinal epithelial cells : EPEC induces tight junction protein redistribution, 10.1111/j.1462-5822.2004.00404.x
Simonovic I., Arpin M., Koutsouris A., Falk-Krzesinski H. J., Hecht G., Enteropathogenic Escherichia coli Activates Ezrin, Which Participates in Disruption of Tight Junction Barrier Function, 10.1128/iai.69.9.5679-5688.2001
Purification of a 20 kDa phosphoprotein from epithelial cells and identification as a myosin light chain Phosphorylation induced by enteropathogenicEscherichia coliand phorbol ester, 10.1016/0014-5793(91)80848-w
Kaper James B., Nataro James P., Mobley Harry L. T., Pathogenic Escherichia coli, 10.1038/nrmicro818
Amasheh S., Claudin-2 expression induces cation-selective channels in tight junctions of epithelial cells, 10.1242/jcs.00165
Rosenthal R., Milatz S., Krug S. M., Oelrich B., Schulzke J.-D., Amasheh S., Gunzel D., Fromm M., Claudin-2, a component of the tight junction, forms a paracellular water channel, 10.1242/jcs.060665
Zeissig S, Burgel N, Gunzel D, Richter J, Mankertz J, Wahnschaffe U, Kroesen A J, Zeitz M, Fromm M, Schulzke J-D, Changes in expression and distribution of claudin 2, 5 and 8 lead to discontinuous tight junctions and barrier dysfunction in active Crohn's disease, 10.1136/gut.2006.094375
Mankertz J., Amasheh M., Krug S. M., Fromm A., Amasheh S., Hillenbrand B., Tavalali S., Fromm M., Schulzke J. D., TNFα up-regulates claudin-2 expression in epithelial HT-29/B6 cells via phosphatidylinositol-3-kinase signaling, 10.1007/s00441-009-0751-8
Dubreuil JD, Curr Issues Mol Biol, 14, 71 (2012)
Okhuysen Pablo C., DuPont Herbert L., EnteroaggregativeEscherichia coli(EAEC): A Cause of Acute and Persistent Diarrhea of Worldwide Importance, 10.1086/654895
Ngendahayo Mukiza C., Dubreuil J. D., Escherichia coli Heat-Stable Toxin b Impairs Intestinal Epithelial Barrier Function by Altering Tight Junction Proteins, 10.1128/iai.00455-13
Bagnoli F., Buti L., Tompkins L., Covacci A., Amieva M. R., Helicobacter pylori CagA induces a transition from polarized to invasive phenotypes in MDCK cells, 10.1073/pnas.0502598102
Fasano A., Baudry B., Pumplin D. W., Wasserman S. S., Tall B. D., Ketley J. M., Kaper J. B., Vibrio cholerae produces a second enterotoxin, which affects intestinal tight junctions., 10.1073/pnas.88.12.5242
GOPALAKRISHNAN S, PANDEY N, TAMIZ A, VERE J, CARRASCO R, SOMERVILLE R, TRIPATHI A, GINSKI M, PATERSON B, ALKAN S, Mechanism of action of ZOT-derived peptide AT-1002, a tight junction regulator and absorption enhancer, 10.1016/j.ijpharm.2008.08.047
Goldblum S. E., Rai U., Tripathi A., Thakar M., De Leo L., Di Toro N., Not T., Ramachandran R., Puche A. C., Hollenberg M. D., Fasano A., The active Zot domain (aa 288-293) increases ZO-1 and myosin 1C serine/threonine phosphorylation, alters interaction between ZO-1 and its binding partners, and induces tight junction disassembly through proteinase activated receptor 2 activation, 10.1096/fj.10-158972
Karczewski J, Am J Physiol Liver Physiol, 298, G851 (2010)
Servin Alain L., Antagonistic activities of lactobacilli and bifidobacteria against microbial pathogens, 10.1016/j.femsre.2004.01.003
McFarland Lynne V., Meta-analysis of probiotics for the prevention of traveler's diarrhea, 10.1016/j.tmaid.2005.10.003
Hermiston M. L., Gordon J. I., Inflammatory Bowel Disease and Adenomas in Mice Expressing a Dominant Negative N-Cadherin, 10.1126/science.270.5239.1203
Nenci Arianna, Becker Christoph, Wullaert Andy, Gareus Ralph, van Loo Geert, Danese Silvio, Huth Marion, Nikolaev Alexei, Neufert Clemens, Madison Blair, Gumucio Deborah, Neurath Markus F., Pasparakis Manolis, Epithelial NEMO links innate immunity to chronic intestinal inflammation, 10.1038/nature05698
Günther Claudia, Martini Eva, Wittkopf Nadine, Amann Kerstin, Weigmann Benno, Neumann Helmut, Waldner Maximilian J., Hedrick Stephen M., Tenzer Stefan, Neurath Markus F., Becker Christoph, Caspase-8 regulates TNF-α-induced epithelial necroptosis and terminal ileitis, 10.1038/nature10400
Takahashi Nozomi, Vereecke Lars, Bertrand Mathieu J. M., Duprez Linde, Berger Scott B., Divert Tatyana, Gonçalves Amanda, Sze Mozes, Gilbert Barbara, Kourula Stephanie, Goossens Vera, Lefebvre Sylvie, Günther Claudia, Becker Christoph, Bertin John, Gough Peter J., Declercq Wim, van Loo Geert, Vandenabeele Peter, RIPK1 ensures intestinal homeostasis by protecting the epithelium against apoptosis, 10.1038/nature13706
Heazlewood Chad K, Cook Matthew C, Eri Rajaraman, Price Gareth R, Tauro Sharyn B, Taupin Douglas, Thornton David J, Png Chin Wen, Crockford Tanya L, Cornall Richard J, Adams Rachel, Kato Masato, Nelms Keats A, Hong Nancy A, Florin Timothy H. J, Goodnow Christopher C, McGuckin Michael A, Aberrant Mucin Assembly in Mice Causes Endoplasmic Reticulum Stress and Spontaneous Inflammation Resembling Ulcerative Colitis, 10.1371/journal.pmed.0050054
Kaser Arthur, Lee Ann-Hwee, Franke Andre, Glickman Jonathan N., Zeissig Sebastian, Tilg Herbert, Nieuwenhuis Edward E.S., Higgins Darren E., Schreiber Stefan, Glimcher Laurie H., Blumberg Richard S., XBP1 Links ER Stress to Intestinal Inflammation and Confers Genetic Risk for Human Inflammatory Bowel Disease, 10.1016/j.cell.2008.07.021
Van der Sluis Maria, De Koning Barbara A.E., De Bruijn Adrianus C.J.M., Velcich Anna, Meijerink Jules P.P., Van Goudoever Johannes B., Büller Hans A., Dekker Jan, Van Seuningen Isabelle, Renes Ingrid B., Einerhand Alexandra W.C., Muc2-Deficient Mice Spontaneously Develop Colitis, Indicating That MUC2 Is Critical for Colonic Protection, 10.1053/j.gastro.2006.04.020
Sovran Bruno, Loonen Linda M. P., Lu Peng, Hugenholtz Floor, Belzer Clara, Stolte Ellen H., Boekschoten Mark V., van Baarlen Peter, Kleerebezem Michiel, de Vos Paul, Dekker Jan, Renes Ingrid B., Wells Jerry M., IL-22-STAT3 Pathway Plays a Key Role in the Maintenance of Ileal Homeostasis in Mice Lacking Secreted Mucus Barrier : , 10.1097/mib.0000000000000319
Glocker Erik-Oliver, Kotlarz Daniel, Boztug Kaan, Gertz E. Michael, Schäffer Alejandro A., Noyan Fatih, Perro Mario, Diestelhorst Jana, Allroth Anna, Murugan Dhaarini, Hätscher Nadine, Pfeifer Dietmar, Sykora Karl-Walter, Sauer Martin, Kreipe Hans, Lacher Martin, Nustede Rainer, Woellner Cristina, Baumann Ulrich, Salzer Ulrich, Koletzko Sibylle, Shah Neil, Segal Anthony W., Sauerbrey Axel, Buderus Stephan, Snapper Scott B., Grimbacher Bodo, Klein Christoph, Inflammatory Bowel Disease and Mutations Affecting the Interleukin-10 Receptor, 10.1056/nejmoa0907206
Duerr R. H., Taylor K. D., Brant S. R., Rioux J. D., Silverberg M. S., Daly M. J., Steinhart A. H., Abraham C., Regueiro M., Griffiths A., Dassopoulos T., Bitton A., Yang H., Targan S., Datta L. W., Kistner E. O., Schumm L. P., Lee A. T., Gregersen P. K., Barmada M. M., Rotter J. I., Nicolae D. L., Cho J. H., A Genome-Wide Association Study Identifies IL23R as an Inflammatory Bowel Disease Gene, 10.1126/science.1135245
Silverberg Mark S, Cho Judy H, Rioux John D, McGovern Dermot P B, Wu Jing, Annese Vito, Achkar Jean-Paul, Goyette Philippe, Scott Regan, Xu Wei, Barmada M Michael, Klei Lambertus, Daly Mark J, Abraham Clara, Bayless Theodore M, Bossa Fabrizio, Griffiths Anne M, Ippoliti Andrew F, Lahaie Raymond G, Latiano Anna, Paré Pierre, Proctor Deborah D, Regueiro Miguel D, Steinhart A Hillary, Targan Stephan R, Schumm L Philip, Kistner Emily O, Lee Annette T, Gregersen Peter K, Rotter Jerome I, Brant Steven R, Taylor Kent D, Roeder Kathryn, Duerr Richard H, Ulcerative colitis–risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study, 10.1038/ng.275
Hilsden RJ, Meddings JB, Sutherland LR, Intestinal permeability changes in response to acetylsalicylic acid in relatives of patients with Crohn's disease, 10.1053/gast.1996.v110.pm8613043
Sinha Atul, Nightingale Jeremy M.D., West Kevin P., Berlanga-Acosta Jorge, Playford Raymond J., Epidermal Growth Factor Enemas with Oral Mesalamine for Mild-to-Moderate Left-Sided Ulcerative Colitis or Proctitis, 10.1056/nejmoa013136
Salim Saʼad Y., Söderholm Johan D., Importance of disrupted intestinal barrier in inflammatory bowel diseases : , 10.1002/ibd.21403
Miquel S, Martín R, Rossi O, Bermúdez-Humarán LG, Chatel JM, Sokol H, Thomas M, Wells JM, Langella P, Faecalibacterium prausnitzii and human intestinal health, 10.1016/j.mib.2013.06.003
Finnie I A, Dwarakanath A D, Taylor B A, Rhodes J M, Colonic mucin synthesis is increased by sodium butyrate., 10.1136/gut.36.1.93
Chassaing Benoit, Darfeuille–Michaud Arlette, The Commensal Microbiota and Enteropathogens in the Pathogenesis of Inflammatory Bowel Diseases, 10.1053/j.gastro.2011.01.054
Wang Jian, Wang Xi, Yang Hong, Wu Dong, Wang Li, Qian Jiaming, Contribution of the IBD5 locus to inflammatory bowel disease: a meta-analysis, 10.1007/s00439-011-0952-6
Noble Colin L., Nimmo Elaine R., Drummond Hazel, Ho Gwo–Tzer, Tenesa Albert, Smith Linda, Anderson Norman, Arnott Ian D.R., Satsangi Jack, The Contribution of OCTN1/2 Variants Within the IBD5 Locus to Disease Susceptibility and Severity in Crohn’s Disease, 10.1053/j.gastro.2005.09.025
Tremelling Mark, Waller Sarah, Bredin Francesca, Greenfield Simon, Parkes Miles, Genetic variants in TNF-α but not DLG5 are associated with inflammatory bowel disease in a large United Kingdom cohort : , 10.1097/01.mib.0000217766.90766.37
Anderson Carl A, Boucher Gabrielle, Lees Charlie W, Franke Andre, D'Amato Mauro, Taylor Kent D, Lee James C, Goyette Philippe, Imielinski Marcin, Latiano Anna, Lagacé Caroline, Scott Regan, Amininejad Leila, Bumpstead Suzannah, Baidoo Leonard, Baldassano Robert N, Barclay Murray, Bayless Theodore M, Brand Stephan, Büning Carsten, Colombel Jean-Frédéric, Denson Lee A, De Vos Martine, Dubinsky Marla, Edwards Cathryn, Ellinghaus David, Fehrmann Rudolf S N, Floyd James A B, Florin Timothy, Franchimont Denis, Franke Lude, Georges Michel, Glas Jürgen, Glazer Nicole L, Guthery Stephen L, Haritunians Talin, Hayward Nicholas K, Hugot Jean-Pierre, Jobin Gilles, Laukens Debby, Lawrance Ian, Lémann Marc, Levine Arie, Libioulle Cecile, Louis Edouard, McGovern Dermot P, Milla Monica, Montgomery Grant W, Morley Katherine I, Mowat Craig, Ng Aylwin, Newman William, Ophoff Roel A, Papi Laura, Palmieri Orazio, Peyrin-Biroulet Laurent, Panés Julián, Phillips Anne, Prescott Natalie J, Proctor Deborah D, Roberts Rebecca, Russell Richard, Rutgeerts Paul, Sanderson Jeremy, Sans Miquel, Schumm Philip, Seibold Frank, Sharma Yashoda, Simms Lisa A, Seielstad Mark, Steinhart A Hillary, Targan Stephan R, van den Berg Leonard H, Vatn Morten, Verspaget Hein, Walters Thomas, Wijmenga Cisca, Wilson David C, Westra Harm-Jan, Xavier Ramnik J, Zhao Zhen Z, Ponsioen Cyriel Y, Andersen Vibeke, Torkvist Leif, Gazouli Maria, Anagnou Nicholas P, Karlsen Tom H, Kupcinskas Limas, Sventoraityte Jurgita, Mansfield John C, Kugathasan Subra, Silverberg Mark S, Halfvarson Jonas, Rotter Jerome I, Mathew Christopher G, Griffiths Anne M, Gearry Richard, Ahmad Tariq, Brant Steven R, Chamaillard Mathias, Satsangi Jack, Cho Judy H, Schreiber Stefan, Daly Mark J, Barrett Jeffrey C, Parkes Miles, Annese Vito, Hakonarson Hakon, Radford-Smith Graham, Duerr Richard H, Vermeire Séverine, Weersma Rinse K, Rioux John D, Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47, 10.1038/ng.764
Darsigny Mathieu, Babeu Jean-Philippe, Dupuis Andrée-Anne, Furth Emma E., Seidman Ernest G., Lévy Émile, Verdu Elena F., Gendron Fernand-Pierre, Boudreau François, Loss of Hepatocyte-Nuclear-Factor-4α Affects Colonic Ion Transport and Causes Chronic Inflammation Resembling Inflammatory Bowel Disease in Mice, 10.1371/journal.pone.0007609
Brooke Matthew A, Longhurst Hilary J, Plagnol Vincent, Kirkby Nicholas S, Mitchell Jane A, Rüschendorf Franz, Warner Timothy D, Kelsell David P, MacDonald Thomas T, Cryptogenic multifocal ulcerating stenosing enteritis associated with homozygous deletion mutations in cytosolic phospholipase A2-α, 10.1136/gutjnl-2012-303581
Ghoshal Uday C, Ranjan Prabhat, Post-infectious irritable bowel syndrome: The past, the present and the future : Post-infectious irritable bowel syndrome, 10.1111/j.1440-1746.2011.06643.x
Fond Guillaume, Loundou Anderson, Hamdani Nora, Boukouaci Wahid, Dargel Aroldo, Oliveira José, Roger Matthieu, Tamouza Ryad, Leboyer Marion, Boyer Laurent, Anxiety and depression comorbidities in irritable bowel syndrome (IBS): a systematic review and meta-analysis, 10.1007/s00406-014-0502-z
Levy Rona L., Olden Kevin W., Naliboff Bruce D., Bradley Laurence A., Francisconi Carlos, Drossman Douglas A., Creed Francis, Psychosocial Aspects of the Functional Gastrointestinal Disorders, 10.1053/j.gastro.2005.11.057
Spiller Robin, Lam Ching, An Update on Post-infectious Irritable Bowel Syndrome: Role of Genetics, Immune Activation, Serotonin and Altered Microbiome, 10.5056/jnm.2012.18.3.258
Ford Alexander C., Talley Nicholas J., Mucosal inflammation as a potential etiological factor in irritable bowel syndrome: a systematic review, 10.1007/s00535-011-0379-9
Steck Natalie, Mueller Kerstin, Schemann Michael, Haller Dirk, Republished: Bacterial proteases in IBD and IBS, 10.1136/postgradmedj-2011-300775rep
Mayer EA, J Clin Psychiatry, 62, 28 (2000)
McKernan D. P., Gaszner G., Quigley E. M., Cryan J. F., Dinan T. G., Altered peripheral toll-like receptor responses in the irritable bowel syndrome : Alterations in toll-like receptor activity in IBS, 10.1111/j.1365-2036.2011.04624.x
Piche T, Barbara G, Aubert P, Bruley des Varannes S, Dainese R, Nano J L, Cremon C, Stanghellini V, De Giorgio R, Galmiche J P, Neunlist M, Impaired intestinal barrier integrity in the colon of patients with irritable bowel syndrome: involvement of soluble mediators, 10.1136/gut.2007.140806
Han Wei, Lu Xuefeng, Jia Xiaoqing, Zhou Tao, Guo Chenghao, Soluble Mediators Released from PI-IBS Patients’ Colon Induced Alteration of Mast Cell: Involvement of Reactive Oxygen Species, 10.1007/s10620-011-1897-2
Chassard C., Dapoigny M., Scott K. P., Crouzet L., Del'homme C., Marquet P., Martin J. C., Pickering G., Ardid D., Eschalier A., Dubray C., Flint H. J., Bernalier-Donadille A., Functional dysbiosis within the gut microbiota of patients with constipated-irritable bowel syndrome, 10.1111/j.1365-2036.2012.05007.x
König J., Brummer R.J., Alteration of the intestinal microbiota as a cause of and a potential therapeutic option in irritable bowel syndrome, 10.3920/bm2013.0033
Rajilić–Stojanović Mirjana, Biagi Elena, Heilig Hans G.H.J., Kajander Kajsa, Kekkonen Riina A., Tims Sebastian, de Vos Willem M., Global and Deep Molecular Analysis of Microbiota Signatures in Fecal Samples From Patients With Irritable Bowel Syndrome, 10.1053/j.gastro.2011.07.043
Saulnier Delphine M., Riehle Kevin, Mistretta Toni–Ann, Diaz Maria–Alejandra, Mandal Debasmita, Raza Sabeen, Weidler Erica M., Qin Xiang, Coarfa Cristian, Milosavljevic Aleksandar, Petrosino Joseph F., Highlander Sarah, Gibbs Richard, Lynch Susan V., Shulman Robert J., Versalovic James, Gastrointestinal Microbiome Signatures of Pediatric Patients With Irritable Bowel Syndrome, 10.1053/j.gastro.2011.06.072
Sundin J., Rangel I., Fuentes S., Heikamp-de Jong I., Hultgren-Hörnquist E., de Vos W. M., Brummer R. J., Altered faecal and mucosal microbial composition in post-infectious irritable bowel syndrome patients correlates with mucosal lymphocyte phenotypes and psychological distress, 10.1111/apt.13055
Brint Elizabeth K, MacSharry John, Fanning Aine, Shanahan Fergus, Quigley Eamonn M M, Differential Expression of Toll-Like Receptors in Patients With Irritable Bowel Syndrome, 10.1038/ajg.2010.438
Zhou QiQi, Zhang Buyi, Verne Nicholas G., Intestinal membrane permeability and hypersensitivity in the irritable bowel syndrome : , 10.1016/j.pain.2009.06.017
Benjamin J L, Hedin C R H, Koutsoumpas A, Ng S C, Hart A L, Kamm M A, Sanderson J D, Knight S C, Forbes A, Stagg A J, Whelan K, Lindsay J O, OC-003 No clinical benefit of prebiotics in the treatment of active Crohn's disease: a double-blind, randomised, placebo-controlled trial:, 10.1136/gut.2009.208934c
Mujagic Z., Ludidi S., Keszthelyi D., Hesselink M. A. M., Kruimel J. W., Lenaerts K., Hanssen N. M. J., Conchillo J. M., Jonkers D. M. A. E., Masclee A. A. M., Small intestinal permeability is increased in diarrhoea predominant IBS, while alterations in gastroduodenal permeability in all IBS subtypes are largely attributable to confounders, 10.1111/apt.12829
Hamer Henrike M., Jonkers Daisy M.A.E., Bast Aalt, Vanhoutvin Steven A.L.W., Fischer Marc A.J.G., Kodde Andrea, Troost Freddy J., Venema Koen, Brummer Robert-Jan M., Butyrate modulates oxidative stress in the colonic mucosa of healthy humans, 10.1016/j.clnu.2008.11.002
HAMER H. M., JONKERS D., VENEMA K., VANHOUTVIN S., TROOST F. J., BRUMMER R.-J., Review article: the role of butyrate on colonic function : REVIEW: ROLE OF BUTYRATE ON COLONIC FUNCTION, 10.1111/j.1365-2036.2007.03562.x
Wallon C, Yang P-C, Keita A V, Ericson A-C, McKay D M, Sherman P M, Perdue M H, Soderholm J D, Corticotropin-releasing hormone (CRH) regulates macromolecular permeability via mast cells in normal human colonic biopsies in vitro, 10.1136/gut.2006.117549
Vanuytsel Tim, van Wanrooy Sander, Vanheel Hanne, Vanormelingen Christophe, Verschueren Sofie, Houben Els, Salim Rasoel Shadea, Tόth Joran, Holvoet Lieselot, Farré Ricard, Van Oudenhove Lukas, Boeckxstaens Guy, Verbeke Kristin, Tack Jan, Psychological stress and corticotropin-releasing hormone increase intestinal permeability in humans by a mast cell-dependent mechanism, 10.1136/gutjnl-2013-305690
Larauche M., Novel insights in the role of peripheral corticotropin-releasing factor and mast cells in stress-induced visceral hypersensitivity : Stress-induced visceral hypersensitivity, 10.1111/j.1365-2982.2011.01867.x
Hubbard C. S., Labus J. S., Bueller J., Stains J., Suyenobu B., Dukes G. E., Kelleher D. L., Tillisch K., Naliboff B. D., Mayer E. A., Corticotropin-Releasing Factor Receptor 1 Antagonist Alters Regional Activation and Effective Connectivity in an Emotional-Arousal Circuit during Expectation of Abdominal Pain, 10.1523/jneurosci.1860-11.2011
Eckardt L., Long-Term Prognosis of Individuals With Right Precordial ST-Segment-Elevation Brugada Syndrome, 10.1161/01.cir.0000153267.21278.8d
Cani P. D., Amar J., Iglesias M. A., Poggi M., Knauf C., Bastelica D., Neyrinck A. M., Fava F., Tuohy K. M., Chabo C., Waget A., Delmee E., Cousin B., Sulpice T., Chamontin B., Ferrieres J., Tanti J.-F., Gibson G. R., Casteilla L., Delzenne N. M., Alessi M. C., Burcelin R., Metabolic Endotoxemia Initiates Obesity and Insulin Resistance, 10.2337/db06-1491
Cani P. D., Bibiloni R., Knauf C., Waget A., Neyrinck A. M., Delzenne N. M., Burcelin R., Changes in Gut Microbiota Control Metabolic Endotoxemia-Induced Inflammation in High-Fat Diet-Induced Obesity and Diabetes in Mice, 10.2337/db07-1403
Everard A., Belzer C., Geurts L., Ouwerkerk J. P., Druart C., Bindels L. B., Guiot Y., Derrien M., Muccioli G. G., Delzenne N. M., de Vos W. M., Cani P. D., Cross-talk between Akkermansia muciniphila and intestinal epithelium controls diet-induced obesity, 10.1073/pnas.1219451110
Everard Amandine, Geurts Lucie, Caesar Robert, Van Hul Matthias, Matamoros Sébastien, Duparc Thibaut, Denis Raphael G. P., Cochez Perrine, Pierard Florian, Castel Julien, Bindels Laure B., Plovier Hubert, Robine Sylvie, Muccioli Giulio G., Renauld Jean-Christophe, Dumoutier Laure, Delzenne Nathalie M., Luquet Serge, Bäckhed Fredrik, Cani Patrice D., Intestinal epithelial MyD88 is a sensor switching host metabolism towards obesity according to nutritional status, 10.1038/ncomms6648
Muccioli Giulio G, Naslain Damien, Bäckhed Fredrik, Reigstad Christopher S, Lambert Didier M, Delzenne Nathalie M, Cani Patrice D, The endocannabinoid system links gut microbiota to adipogenesis, 10.1038/msb.2010.46
Chassaing Benoit, Koren Omry, Goodrich Julia K., Poole Angela C., Srinivasan Shanthi, Ley Ruth E., Gewirtz Andrew T., Dietary emulsifiers impact the mouse gut microbiota promoting colitis and metabolic syndrome, 10.1038/nature14232
Cani Patrice D, Van Hul Matthias, Novel opportunities for next-generation probiotics targeting metabolic syndrome, 10.1016/j.copbio.2014.10.006
Erridge C, Am J Clin Nutr, 86, 1286 (2007)
Amar J, Am J Clin Nutr, 87, 1219 (2008)
Laugerette Fabienne, Vors Cécile, Géloën Alain, Chauvin Marie-Agnès, Soulage Christophe, Lambert-Porcheron Stéphanie, Peretti Noël, Alligier Maud, Burcelin Rémy, Laville Martine, Vidal Hubert, Michalski Marie-Caroline, Emulsified lipids increase endotoxemia: possible role in early postprandial low-grade inflammation, 10.1016/j.jnutbio.2009.11.011
Deopurkar R., Ghanim H., Friedman J., Abuaysheh S., Sia C. L., Mohanty P., Viswanathan P., Chaudhuri A., Dandona P., Differential Effects of Cream, Glucose, and Orange Juice on Inflammation, Endotoxin, and the Expression of Toll-Like Receptor-4 and Suppressor of Cytokine Signaling-3, 10.2337/dc09-1630
Ghanim H., Abuaysheh S., Sia C. L., Korzeniewski K., Chaudhuri A., Fernandez-Real J. M., Dandona P., Increase in Plasma Endotoxin Concentrations and the Expression of Toll-Like Receptors and Suppressor of Cytokine Signaling-3 in Mononuclear Cells After a High-Fat, High-Carbohydrate Meal: Implications for insulin resistance, 10.2337/dc09-0979
Anderson Paul D., Mehta Nehal N., Wolfe Megan L., Hinkle Christine C., Pruscino Leticia, Comiskey Lynne L., Tabita-Martinez Jennifer, Sellers Kimberly F., Rickels Michael R., Ahima Rexford S., Reilly Muredach P., Innate Immunity Modulates Adipokines in Humans, 10.1210/jc.2006-2545
Creely S. J., McTernan P. G., Kusminski C. M., Fisher ff. M., Da Silva N. F., Khanolkar M., Evans M., Harte A. L., Kumar S., Lipopolysaccharide activates an innate immune system response in human adipose tissue in obesity and type 2 diabetes, 10.1152/ajpendo.00302.2006
Pussinen P. J., Havulinna A. S., Lehto M., Sundvall J., Salomaa V., Endotoxemia Is Associated With an Increased Risk of Incident Diabetes, 10.2337/dc10-1676
Al-Attas Omar S, Al-Daghri Nasser M, Al-Rubeaan Khalid, da Silva Nancy F, Sabico Shaun L, Kumar Sudhesh, McTernan Philip G, Harte Alison L, Changes in endotoxin levels in T2DM subjects on anti-diabetic therapies, 10.1186/1475-2840-8-20
Nolan JP, Gastroenterology, 69, 1346 (1975)
Nolan JP, Gastroenterology, 75, 765 (1978)
Bedogni Giorgio, Miglioli Lucia, Masutti Flora, Tiribelli Claudio, Marchesini Giulio, Bellentani Stefano, Prevalence of and risk factors for nonalcoholic fatty liver disease: The Dionysos nutrition and liver study, 10.1002/hep.20734
Farhadi Ashkan, Gundlapalli Sushama, Shaikh Maliha, Frantzides Constantine, Harrell Laura, Kwasny Mary M., Keshavarzian Ali, Susceptibility to gut leakiness: a possible mechanism for endotoxaemia in non-alcoholic steatohepatitis : Gut leakiness and NASH, 10.1111/j.1478-3231.2008.01723.x
Miele Luca, Valenza Venanzio, La Torre Giuseppe, Montalto Massimo, Cammarota Giovanni, Ricci Riccardo, Mascianà Roberta, Forgione Alessandra, Gabrieli Maria L., Perotti Germano, Vecchio Fabio M., Rapaccini Gianlodovico, Gasbarrini Giovanni, Day Chris P., Grieco Antonio, Increased intestinal permeability and tight junction alterations in nonalcoholic fatty liver disease, 10.1002/hep.22848
Gummesson Anders, Carlsson Lena M.S., Storlien Len H., Bäckhed Fredrik, Lundin Pål, Löfgren Lars, Stenlöf Kaj, Lam Yan Y., Fagerberg Björn, Carlsson Björn, Intestinal Permeability Is Associated With Visceral Adiposity in Healthy Women, 10.1038/oby.2011.251
Brignardello J., Morales P., Diaz E., Romero J., Brunser O., Gotteland M., Pilot study: alterations of intestinal microbiota in obese humans are not associated with colonic inflammation or disturbances of barrier function : Gut microbiota and permeability in obese subjects, 10.1111/j.1365-2036.2010.04475.x
Schulzke Jörg-Dieter, Bentzel Carl J, Schulzke Ines, Riecken Ernst-Otto, Fromm Michael, Epithelial Tight Junction Structure in the Jejunum of Children with Acute and Treated Celiac Sprue, 10.1203/00006450-199804000-00001
Montalto Massimo, Cuoco Lucio, Ricci Riccardo, Maggiano Nicola, Vecchio Fabio Maria, Gasbarrini Giovanni, Immunohistochemical Analysis of ZO-1 in the Duodenal Mucosa of Patients with Untreated and Treated Celiac Disease, 10.1159/000063817
Pizzuti D., Bortolami M., Mazzon E., Buda A., Guariso G., D’Odorico A., Chiarelli S., D’Incà R., De Lazzari F., Martines D., Transcriptional downregulation of tight junction protein ZO-1 in active coeliac disease is reversed after a gluten-free diet, 10.1016/j.dld.2004.01.013
Bjarnason Ingvar, Peters TimothyJ., Veall Norman, A PERSISTENT DEFECT IN INTESTINAL PERMEABILITY IN COELIAC DISEASE DEMONSTRATED BY A 51Cr-LABELLED EDTA ABSORPTION TEST, 10.1016/s0140-6736(83)91628-8
Duerksen D. R., Wilhelm-Boyles C., Parry D. M., Intestinal Permeability in Long-Term Follow-up of Patients with Celiac Disease on a Gluten-Free Diet, 10.1007/s10620-005-2574-0
Heyman Martine, Abed Juliette, Lebreton Corinne, Cerf-Bensussan Nadine, Intestinal permeability in coeliac disease: insight into mechanisms and relevance to pathogenesis, 10.1136/gutjnl-2011-300327
van Elburg R M, Uil J J, Mulder C J, Heymans H S, Intestinal permeability in patients with coeliac disease and relatives of patients with coeliac disease., 10.1136/gut.34.3.354
Drago Sandro, El Asmar Ramzi, Di Pierro Mariarosaria, Grazia Clemente Maria, Sapone Amit Tripathi Anna, Thakar Manjusha, Iacono Giuseppe, Carroccio Antonio, D'Agate Cinzia, Not Tarcisio, Zampini Lucia, Catassi Carlo, Fasano Alessio, Gliadin, zonulin and gut permeability: Effects on celiac and non-celiac intestinal mucosa and intestinal cell lines, 10.1080/00365520500235334
Sander Guy R., Cummins Adrian G., Powell Barry C., Rapid disruption of intestinal barrier function by gliadin involves altered expression of apical junctional proteins, 10.1016/j.febslet.2005.07.066
Clemente M G, Early effects of gliadin on enterocyte intracellular signalling involved in intestinal barrier function, 10.1136/gut.52.2.218
Lammers Karen M., Lu Ruliang, Brownley Julie, Lu Bao, Gerard Craig, Thomas Karen, Rallabhandi Prasad, Shea-Donohue Terez, Tamiz Amir, Alkan Sefik, Netzel–Arnett Sarah, Antalis Toni, Vogel Stefanie N., Fasano Alessio, Gliadin Induces an Increase in Intestinal Permeability and Zonulin Release by Binding to the Chemokine Receptor CXCR3, 10.1053/j.gastro.2008.03.023
Fasano Alessio, Not Tarcisio, Wang Wenle, Uzzau Sergio, Berti Irene, Tommasini Alberto, Goldblum Simeon E, Zonulin, a newly discovered modulator of intestinal permeability, and its expression in coeliac disease, 10.1016/s0140-6736(00)02169-3
Sapone Anna, Bai Julio C, Ciacci Carolina, Dolinsek Jernej, Green Peter HR, Hadjivassiliou Marios, Kaukinen Katri, Rostami Kamran, Sanders David S, Schumann Michael, Ullrich Reiner, Villalta Danilo, Volta Umberto, Catassi Carlo, Fasano Alessio, Spectrum of gluten-related disorders: consensus on new nomenclature and classification, 10.1186/1741-7015-10-13
Huebener Sina, Tanaka Charlene K., Uhde Melanie, Zone John J., Vensel William H., Kasarda Donald D., Beams Leilani, Briani Chiara, Green Peter H. R., Altenbach Susan B., Alaedini Armin, Specific Nongluten Proteins of Wheat Are Novel Target Antigens in Celiac Disease Humoral Response, 10.1021/pr500809b
Sapone Anna, Lammers Karen M, Casolaro Vincenzo, Cammarota Marcella, Giuliano Maria Teresa, De Rosa Mario, Stefanile Rosita, Mazzarella Giuseppe, Tolone Carlo, Russo Maria Itria, Esposito Pasquale, Ferraraccio Franca, Cartenì Maria, Riegler Gabriele, de Magistris Laura, Fasano Alessio, Divergence of gut permeability and mucosal immune gene expression in two gluten-associated conditions: celiac disease and gluten sensitivity, 10.1186/1741-7015-9-23
Brottveit Margit, Beitnes Ann-Christin R, Tollefsen Stig, Bratlie Jorunn E, Jahnsen Frode L, Johansen Finn-Eirik, Sollid Ludvig M, Lundin Knut E A, Mucosal Cytokine Response After Short-Term Gluten Challenge in Celiac Disease and Non-Celiac Gluten Sensitivity, 10.1038/ajg.2013.91
Hollon Justin, Puppa Elaine, Greenwald Bruce, Goldberg Eric, Guerrerio Anthony, Fasano Alessio, Effect of Gliadin on Permeability of Intestinal Biopsy Explants from Celiac Disease Patients and Patients with Non-Celiac Gluten Sensitivity, 10.3390/nu7031565
Andre C, Ann Allergy, 59, 127 (1987)
Ventura M.T., Polimeno L., Amoruso A.C., Gatti F., Annoscia E., Marinaro M., Di Leo E., Matino M.G., Buquicchio R., Bonini S., Tursi A., Francavilla A., Intestinal permeability in patients with adverse reactions to food, 10.1016/j.dld.2006.06.012
Perrier C., Corthésy B., Gut permeability and food allergies : Gut permeability and food allergies, 10.1111/j.1365-2222.2010.03639.x
Järvinen Kirsi M., Konstantinou George N., Pilapil Mariecel, Arrieta Marie-Claire, Noone Sally, Sampson Hugh A., Meddings Jon, Nowak-Węgrzyn Anna, Intestinal permeability in children with food allergy on specific elimination diets, 10.1111/pai.12106
Mullin James M., Gabello Melissa, Murray Lisa J., Farrell Christopher P., Bellows Jillan, Wolov Kevin R., Kearney Keith R., Rudolph David, Thornton James J., Proton pump inhibitors: actions and reactions, 10.1016/j.drudis.2009.03.014
Keszthelyi D., Jansen S. V., Schouten G. A., De Kort S., Scholtes B., Engels L. G. J. B., Masclee A. A. M., Proton pump inhibitor use is associated with an increased risk for microscopic colitis: a case-control study : Proton pump inhibitors and microscopic colitis, 10.1111/j.1365-2036.2010.04453.x
Aydin Cengiz, Sarac B�lent, Koyuncu Ayhan, Yildirim Sahin, Sen Metin, Sarioglu Yusuf, Relaxant effect of omeprazole and lansoprazole in guinea pig gallbladder muscle strips in vitro, 10.1007/s00535-003-1143-6
Gabello Melissa, Omeprazole induces gastric transmucosal permeability to the peptide bradykinin, 10.3748/wjg.v16.i9.1097
Murray Lisa J., Gabello Melissa, Rudolph David S., Farrell Christopher P., Morgan Melissa, Martin Aaron P., Underwood James C., Valenzano M. Carmen, Mullin James M., Transmucosal Gastric Leak Induced by Proton Pump Inhibitors, 10.1007/s10620-008-0528-z
Hopkins Ann M., McDonnell Ciara, Breslin Niall P., O'Morain Colm A., Baird Alan W., Omeprazole increases permeability across isolated rat gastric mucosa pre-treated with an acid secretagogue, 10.1211/0022357021778583
MULLIN J. M., VALENZANO M. C., WHITBY M., LURIE D., SCHMIDT J. D., JAIN V., TULLY O., KEARNEY K., LAZOWICK D., MERCOGLIANO G., THORNTON J. J., Esomeprazole induces upper gastrointestinal tract transmucosal permeability increase, 10.1111/j.1365-2036.2008.03824.x
Gabello M., Valenzano M. C., Barr M., Zurbach P., Mullin J. M., Omeprazole Induces Gastric Permeability to Digoxin, 10.1007/s10620-009-0851-z
YENISEHIRLI A, ONUR R, Specific H+/K+-ATPase inhibitors decreased contractile responses of isolated rat vas deferens, 10.1016/j.phrs.2006.07.005
Tachechi I, Acta Med, 53, 3 (2010)
Higuchi Kazuhide, Umegaki Eiji, Watanabe Toshio, Yoda Yukiko, Morita Eijiro, Murano Mitsuyuki, Tokioka Satoshi, Arakawa Tetsuo, Present status and strategy of NSAIDs-induced small bowel injury, 10.1007/s00535-009-0102-2
Bjarnason Ingvar, So Alex, Levi A.Jonathan, Peters TimothyJ., Williams Peter, Zanelli GiuseppeD., Gumpel J.Michael, Ansell Barbara, INTESTINAL PERMEABILITY AND INFLAMMATION IN RHEUMATOID ARTHRITIS: EFFECTS OF NON-STEROIDAL ANTI-INFLAMMATORY DRUGS, 10.1016/s0140-6736(84)92739-9
Bjarnason I., Price A.B., Zanelli G., Smethurst P., Burke M., Gumpel J.M., Levi A.J., Clinicopathological features of nonsteroidal antiinflammatory drug-induced small intestinal strictures, 10.1016/0016-5085(88)90568-9
Darling Rebecca L., Romero Jimmy J., Dial Elizabeth J., Akunda Jacqueline K., Langenbach Robert, Lichtenberger Lenard M., The effects of aspirin on gastric mucosal integrity, surface hydrophobicity, and prostaglandin metabolism in cyclooxygenase knockout mice, 10.1053/j.gastro.2004.04.003
Somasundaram, Sigthorsson, Simpson, Watts, Jacob, Tavares, Rafi, Roseth, Foster, Price, Wrigglesworth, Bjarnason, Uncoupling of intestinal mitochondrial oxidative phosphorylation and inhibition of cyclooxygenase are required for the development of NSAID-enteropathy in the rat, 10.1046/j.1365-2036.2000.00723.x
Somasundaram S, Rafi S, Hayllar J, Sigthorsson G, Jacob M, Price A B, Macpherson A, Mahmod T, Scott D, Wrigglesworth J M, Bjarnason I, Mitochondrial damage: a possible mechanism of the "topical" phase of NSAID induced injury to the rat intestine, 10.1136/gut.41.3.344
Fortun Paul James, Hawkey Christopher John, Nonsteroidal antiinflammatory drugs and the small intestine : , 10.1097/01.mog.0000153314.51198.58
Reuter BK, Davies NM, Wallace JL, Nonsteroidal anti-inflammatory drug enteropathy in rats: Role of permeability, bacteria, and enterohepatic circulation, 10.1016/s0016-5085(97)70225-7
Scarpignato C, NSAID-induced intestinal damage: are luminal bacteria the therapeutic target?, 10.1136/gut.2007.134502
Bjarnason I, Williams P, Smethurst P, Peters T J, Levi A J, Effect of non-steroidal anti-inflammatory drugs and prostaglandins on the permeability of the human small intestine., 10.1136/gut.27.11.1292
Sigthorsson Gudmundur, Simpson Robert J., Walley Matthew, Anthony Andrew, Foster Russell, Hotz–Behoftsitz Christoph, Palizban Abbas, Pombo Joaquim, Watts Jo, Morham Scott G., Bjarnason Ingvar, COX-1 and 2, intestinal integrity, and pathogenesis of nonsteroidal anti-inflammatory drug enteropathy in mice, 10.1053/gast.2002.33647
Smecuol E, Acute gastrointestinal permeability responses to different non-steroidal anti-inflammatory drugs, 10.1136/gut.49.5.650
Bjarnason Ingvar, Takeuchi Ken, Intestinal permeability in the pathogenesis of NSAID-induced enteropathy, 10.1007/s00535-008-2266-6
Bjarnason Ingvar, Prouse Peter, Smith Terry, Gumpel MichaelJ, Zanelli Guiseppe, Smethurst Paul, Levi Sassoon, Levi A.Jonathan, BLOOD AND PROTEIN LOSS VIA SMALL-INTESTINAL INFLAMMATION INDUCED BY NON-STEROIDAL ANTI-INFLAMMATORY DRUGS, 10.1016/s0140-6736(87)91075-0
Langman M J, Morgan L, Worrall A, Use of anti-inflammatory drugs by patients admitted with small or large bowel perforations and haemorrhage., 10.1136/bmj.290.6465.347
Bjarnason Ingvar, Smethurst Paul, Fenn Christopher G., Lee Carole E., Menzies Ian S., Levi A. Jonathan, Misoprostol reduces indomethacin-induced changes in human small intestinal permeability, 10.1007/bf01536263
Davies Gareth R., Wilkie Martin E., Rampton David S., Effects of metronidazole and misoprostol on indomethacin-induced changes in intestinal permeability, 10.1007/bf01316493
MORRIS A. J., MURRAY L., STURROCK R. D., MADHOK R., CAPELL H. A., MACKENZIE J. F., Short report: the effect of misoprostol on the anaemia of NSAID enteropathy, 10.1111/j.1365-2036.1994.tb00298.x
Bours Martijn J., Troost Freddy J., Brummer Robert-Jan M., Bast Aalt, Dagnelie Pieter C., Local effect of adenosine 5???-triphosphate on indomethacin-induced permeability changes in the human small intestine : , 10.1097/meg.0b013e328011093c
Bours Martijn JL, Bos Hilde J, Meddings Jon B, Brummer Robert-Jan M, van den Brandt Piet A, Dagnelie Pieter C, Effects of oral adenosine 5'-triphosphate and adenosine in enteric-coated capsules on indomethacin-induced permeability changes in the human small intestine: a randomized cross-over study, 10.1186/1471-230x-7-23
Troost F J, Saris W H M, Brummer R-J M, Recombinant human lactoferrin ingestion attenuates indomethacin-induced enteropathy in vivo in healthy volunteers, 10.1038/sj.ejcn.1601727
van Wijck Kim, Verlinden Thomas J.M., van Eijk Hans M.H., Dekker Jan, Buurman Wim A., Dejong Cornelis H.C., Lenaerts Kaatje, Novel multi-sugar assay for site-specific gastrointestinal permeability analysis: A randomized controlled crossover trial, 10.1016/j.clnu.2012.06.014
de Magistris Laura, Familiari Valeria, Pascotto Antonio, Sapone Anna, Frolli Alessandro, Iardino Patrizia, Carteni Maria, De Rosa Mario, Francavilla Ruggiero, Riegler Gabriele, Militerni Roberto, Bravaccio Carmela, Alterations of the Intestinal Barrier in Patients With Autism Spectrum Disorders and in Their First-degree Relatives : , 10.1097/mpg.0b013e3181dcc4a5
Maes Michael, Kubera Marta, Leunis Jean-Claude, Berk Michael, Increased IgA and IgM responses against gut commensals in chronic depression: Further evidence for increased bacterial translocation or leaky gut, 10.1016/j.jad.2012.02.023
Severance Emily G., Yolken Robert H., Eaton William W., Autoimmune diseases, gastrointestinal disorders and the microbiome in schizophrenia: more than a gut feeling, 10.1016/j.schres.2014.06.027
Severance Emily G., Gressitt Kristin L., Stallings Cassie R., Origoni Andrea E., Khushalani Sunil, Leweke F. Markus, Dickerson Faith B., Yolken Robert H., Discordant patterns of bacterial translocation markers and implications for innate immune imbalances in schizophrenia, 10.1016/j.schres.2013.05.018
Berk Michael, Williams Lana J, Jacka Felice N, O’Neil Adrienne, Pasco Julie A, Moylan Steven, Allen Nicholas B, Stuart Amanda L, Hayley Amie C, Byrne Michelle L, Maes Michael, So depression is an inflammatory disease, but where does the inflammation come from?, 10.1186/1741-7015-11-200
Bjarnason Ingvar, Ward Kevin, Peters TimothyJ, THE LEAKY GUT OF ALCOHOLISM: POSSIBLE ROUTE OF ENTRY FOR TOXIC COMPOUNDS, 10.1016/s0140-6736(84)92109-3
Pals KL, J Appl Physiol, 82, 571 (1997)
van Nieuwenhoven Michiel A., Brouns Fred, Brummer Robert-Jan M., Gastrointestinal profile of symptomatic athletes at rest and during physical exercise, 10.1007/s00421-003-1007-z
Maxton D. G., Menzies I. S., Slavin B., Thompson R. P. H., Small-Intestinal Function during Enteral Feeding and Starvation in Man, 10.1042/cs0770401
Dean Paul, Kenny Brendan, Intestinal barrier dysfunction by enteropathogenic Escherichia coli is mediated by two effector molecules and a bacterial surface protein : Intestinal barrier disrupting proteins of EPEC, 10.1111/j.1365-2958.2004.04308.x
Viswanathan V. K., Koutsouris A., Lukic S., Pilkinton M., Simonovic I., Simonovic M., Hecht G., Comparative Analysis of EspF from Enteropathogenic and Enterohemorrhagic Escherichia coli in Alteration of Epithelial Barrier Function, 10.1128/iai.72.6.3218-3227.2004
Roxas Jennifer L, Koutsouris Athanasia, Bellmeyer Amy, Tesfay Samuel, Royan Sandhya, Falzari Kanakeshwari, Harris Antoneicka, Cheng Hao, Rhee Ki Jong, Hecht Gail, Enterohemorrhagic E. coli alters murine intestinal epithelial tight junction protein expression and barrier function in a Shiga toxin independent manner, 10.1038/labinvest.2010.91
Bertelsen L. S., Modulation of chloride secretory responses and barrier function of intestinal epithelial cells by the Salmonella effector protein SigD, 10.1152/ajpcell.00413.2003
Boyle Erin C., Brown Nat F., Finlay B. Brett, Salmonella enterica serovar Typhimurium effectors SopB, SopE, SopE2 and SipA disrupt tight junction structure and function, 10.1111/j.1462-5822.2006.00762.x
Amieva M. R., Disruption of the Epithelial Apical-Junctional Complex by Helicobacter pylori CagA, 10.1126/science.1081919
Krueger Sabine, Hundertmark Tanja, Kuester Doerthe, Kalinski Thomas, Peitz Ulrich, Roessner Albert, Helicobacter pylori alters the distribution of ZO-1 and p120ctn in primary human gastric epithelial cells, 10.1016/j.prp.2007.04.003
Romanov Victor, Whyard Terry C., Waltzer Wayne C., Gabig Theodore G., A claudin 3 and claudin 4-targeted Clostridium perfringens protoxin is selectively cytotoxic to PSA-producing prostate cancer cells, 10.1016/j.canlet.2014.06.009
Forrest J. Craig, Campbell Jacquelyn A., Schelling Pierre, Stehle Thilo, Dermody Terence S., Structure-Function Analysis of Reovirus Binding to Junctional Adhesion Molecule 1 : IMPLICATIONS FOR THE MECHANISM OF REOVIRUS ATTACHMENT, 10.1074/jbc.m305649200
López Susana, Arias Carlos F., Multistep entry of rotavirus into cells: a Versaillesque dance, 10.1016/j.tim.2004.04.003
Nava P., The rotavirus surface protein VP8 modulates the gate and fence function of tight junctions in epithelial cells, 10.1242/jcs.01425
Bibliographic reference
König, Julia ; Wells, Jerry ; Cani, Patrice D. ; García-Ródenas, Clara L ; MacDonald, Tom ; et. al. Human Intestinal Barrier Function in Health and Disease.. In: Clinical and Translational Gastroenterology, Vol. 7, no.10, p. e196 [1-13] (2016)