Bacteria Penetrate the Inner Mucus Layer before Inflammation in the Dextran Sulfate Colitis Model
Open accessAbstract
BACKGROUND: Protection of the large intestine with its enormous amount of commensal bacteria is a challenge that became easier to understand when we recently could describe that colon has an inner attached mucus layer devoid of bacteria (Johansson et al. (2008) Proc. Natl. Acad. Sci. USA 105, 15064-15069). The bacteria are thus kept at a distance from the epithelial cells and lack of this layer, as in Muc2-null mice, allow bacteria to contact the epithelium. This causes colitis and later on colon cancer, similar to the human disease Ulcerative Colitis, a disease that still lacks a pathogenetic explanation. Dextran Sulfate (DSS) in the drinking water is the most widely used animal model for experimental colitis. In this model, the inflammation is observed after 3-5 days, but early events explaining why DSS causes this has not been described. PRINCIPAL FINDINGS: When mucus formed on top of colon explant cultures were exposed to 3% DSS, the thickness of the inner mucus layer decreased and became permeable to 2 microm fluorescent beads after 15 min. Both DSS and Dextran readily penetrated the mucus, but Dextran had no effect on thickness or permeability. When DSS was given in the drinking water to mice and the colon was stained for bacteria and the Muc2 mucin, bacteria were shown to penetrate the inner mucus layer and reach the epithelial cells already within 12 hours, long before any infiltration of inflammatory cells. CONCLUSION: DSS thus causes quick alterations in the inner colon mucus layer that makes it permeable to bacteria. The bacteria that reach the epithelial cells probably trigger an inflammatory reaction. These observations suggest that altered properties or lack of the inner colon mucus layer may be an initial event in the development of colitis.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Failure of the protective barrier to separate bacteria from the epithelium is observed in several murine colitis models.
“Failure of this protective barrier to separate bacteria from the epithelium is observed in a number of murine colitis models 15, 17.”
From The composition of the gut microbiota shapes the colon mucus barrier (2015) · cites this paper as [17]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Recognition of Commensal Microflora by Toll-Like Receptors Is Required for Intestinal Homeostasis
Rakoff-Nahoum, S., Paglino, J., Eslami-Varzaneh, F., Edberg, S., & Medzhitov, R. (2004) · Cell · doi:10.1016/j.cell.2004.07.002 · Cited by 4,251 · see citing works
Intestinal mucosal barrier function in health and disease
Turner, J. R. (2009) · Nature reviews. Immunology · doi:10.1038/nri2653 · Cited by 3,952 · see citing works
Okayasu, I., Hatakeyama, S., Yamada, M., Ohkusa, T., Inagaki, Y., & NAKAYA, R. (1990) · Gastroenterology · doi:10.1016/0016-5085(90)90290-h · Cited by 2,405 · see citing works
The inner of the two Muc2 mucin-dependent mucus layers in colon is devoid of bacteria
Johansson, M. E. V., Phillipson, M., Petersson, J., Velcich, A., Holm, L., & Hansson, G. C. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0803124105 · Cited by 2,200 · see citing works
Self-citationClinicopathologic study of dextran sulfate sodium experimental acute colitis
Shichijo, K., Matuu, M., Ikeda, Y., Naito, S., Ito, M., & Sekine, I. (1998) · The Japanese Journal of Pharmacology · doi:10.1016/s0021-5198(19)41298-5 · Cited by 1,943 · see citing works
Van der Sluis, M., De Koning, B. A. E., De Bruijn, A. C. J. M., Velcich, A., Meijerink, J. P. P., Van Goudoever, J. B., Büller, H. A., Dekker, J., Van Seuningen, I., Renes, I. B., et al. (2006) · Gastroenterology · doi:10.1053/j.gastro.2006.04.020 · Cited by 1,684 · see citing works
The adherent gastrointestinal mucus gel layer: thickness and physical state in vivo
Atuma, C., Strugala, V., Allen, A., & Holm, L. (2001) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.2001.280.5.g922 · Cited by 1,083 · see citing works
Self-citationColorectal Cancer in Mice Genetically Deficient in the Mucin Muc2
Velcich, A., Yang, W., Heyer, J., Fragale, A., Nicholas, C., Viani, S., Kucherlapati, R., Lipkin, M., Yang, K., & Augenlicht, L. (2002) · Science · doi:10.1126/science.1069094 · Cited by 936 · see citing works
Heazlewood, C. K., Cook, M. C., Eri, R., Price, G. R., Tauro, S. B., Taupin, D., Thornton, D. J., Png, C. W., Crockford, T. L., Cornall, R. J., et al. (2008) · PLoS Medicine · doi:10.1371/journal.pmed.0050054 · Cited by 701 · see citing works
Inflammatory Bowel Disease and Adenomas in Mice Expressing a Dominant Negative N-Cadherin
Hermiston, M. L., & Gordon, J. I. (1995) · Science · doi:10.1126/science.270.5239.1203 · Cited by 669 · see citing works
Yan, Y., Kolachala, V. L., Dalmasso, G., Nguyen, H. T. T., Laroui, H., Sitaraman, S. V., & Merlin, D. (2009) · PLoS ONE · doi:10.1371/journal.pone.0006073 · Cited by 412 · see citing works
Differential susceptibility of inbred mouse strains to dextran sulfate sodium-induced colitis
Mähler, M., Bristol, I. J., Leiter, E. H., Workman, A. E., Birkenmeier, E. H., Elson, C. O., & Sundberg, J. P. (1998) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1998.274.3.g544 · Cited by 401 · see citing works
Increased susceptibility to colitis and colorectal tumors in mice lacking core 3–derived O-glycans
An, G., Wei, B., Xia, B., McDaniel, J. M., Ju, T., Cummings, R. D., Braun, J., & Xia, L. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20061929 · Cited by 352 · see citing works
Animal models of inflammatory bowel disease
Jurjus, A. R., Khoury, N. N., & Reimund, J. (2004) · Journal of Pharmacological and Toxicological Methods · doi:10.1016/j.vascn.2003.12.002 · Cited by 338 · see citing works
Gel-forming mucins appeared early in metazoan evolution
Lang, T., Hansson, G. C., & Samuelsson, T. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0705984104 · Cited by 310 · see citing works
Self-citationLarsson, J. M. H., Karlsson, H., Sjövall, H., & Hansson, G. C. (2009) · Glycobiology · doi:10.1093/glycob/cwp048 · Cited by 282 · see citing works
Self-citationThe inner of the two Muc2 mucin-dependent mucus layers in colon is devoid of bacteria
Hansson, G. C., & Johansson, M. (2010) · Gut Microbes · doi:10.4161/gmic.1.1.10470 · Cited by 267 · see citing works
Self-citationJohansson, M., Thomsson, K. A., & Hansson, G. C. (2009) · Journal of Proteome Research · doi:10.1021/pr9002504 · Cited by 237 · see citing works
Self-citationGodl, K., Johansson, M., Lidell, M. E., Mörgelin, M., Karlsson, H., Olson, F. J., Gum, J. R., Kim, Y. S., & Hansson, G. C. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m208483200 · Cited by 212 · see citing works
Self-citationKitajima, S., TAKUMA, S., & MORIMOTO, M. (2000) · EXPERIMENTAL ANIMALS · doi:10.1538/expanim.49.9 · Cited by 207 · see citing works
Schulz, B. L., Packer, N. H., & Karlsson, N. G. (2002) · Analytical Chemistry · doi:10.1021/ac025890a · Cited by 203 · see citing works
Axelsson, L. ‐., Landström, E., Goldschmidt, T. J., Grönberg, A., & Bylund‐Fellenius, A. (1996) · Inflammation Research · doi:10.1007/bf02285159 · Cited by 174 · see citing works
Dextran Sodium Sulfate-Induced Colitis in Germ-Free IQI/Jic Mice.
Kitajima, S., MORIMOTO, M., Sagara, E., SHIMIZU, C., & IKEDA, Y. (2001) · EXPERIMENTAL ANIMALS · doi:10.1538/expanim.50.387 · Cited by 168 · see citing works
Asker, N., Axelsson, M., Olofsson, S., & Hansson, G. C. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.30.18857 · Cited by 154 · see citing works
Self-citationDawson, P. A., Huxley, S., Gardiner, B., Tran, T., McAuley, J., Grimmond, S. M., McGuckin, M. A., & Markovich, D. (2009) · Gut · doi:10.1136/gut.2007.147595 · Cited by 131 · see citing works
Axelsson, M., Asker, N., & Hansson, G. C. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.30.18864 · Cited by 113 · see citing works
Self-citationA new role for cathelicidin in ulcerative colitis in mice.
Tai, E. K. K., Wu, W. K. K., Wong, H. P. S., Lam, E. K. Y., Yu, L., & Cho, C. H. (2007) · PubMed · doi:10.3181/00379727-232-2320799 · Cited by 74 · see citing works
Acid transport through channels in the mucous layer of rat stomach
Johansson, M., Synnerstad, I., & Holm, L. P. (2000) · Gastroenterology · doi:10.1053/gast.2000.19455 · Cited by 66 · see citing works
Self-citationMalmberg, E., Noaksson, K. A., Phillipson, M., Johansson, M., Hinojosa-Kurtzberg, M., Holm, L. P., Gendler, S. J., & Hansson, G. C. (2006) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00491.2005 · Cited by 65 · see citing works
Self-citationAlterations in Muc2 biosynthesis and secretion during dextran sulfate sodium-induced colitis
Renes, I. B., Boshuizen, J. A., Nispen, D. J. P. M. V., Bulsing, N. P., Büller, H. A., Dekker, J. P., & Einerhand, A. W. C. (2002) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00229.2001 · Cited by 54 · see citing works
COLONIC ULCERATION IN YOUNG RATS FED DEGRADED CARRAGEENAN
Marcus, R., & Watt, J. (1971) · The Lancet · doi:10.1016/s0140-6736(71)92130-1 · Cited by 47 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
The gastrointestinal mucus system in health and disease
Johansson, M. E. V., Sjövall, H., & Hansson, G. C. (2013) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2013.35 · Cited by 1,438 · see citing works
Self-citationIntestinal Goblet Cells and Mucins in Health and Disease: Recent Insights and Progress
Kim, Y. S., & Ho, S. B. (2010) · Current Gastroenterology Reports · doi:10.1007/s11894-010-0131-2 · Cited by 1,437 · see citing works
Pelaseyed, T., Bergström, J. H., Gustafsson, J. K., Ermund, A., Birchenough, G. M. H., Schütte, A., van der Post, S., Svensson, F., Rodríguez‐Piñeiro, A. M., Nyström, E. E. L., et al. (2014) · Immunological Reviews · doi:10.1111/imr.12182 · Cited by 1,363 · see citing works
Self-citationJohansson, M. E. V., Gustafsson, J. K., Holmén-Larsson, J., Jabbar, K. S., Xia, L., Xu, H., Ghishan, F. K., Carvalho, F. A., Gewirtz, A. T., Sjövall, H., et al. (2014) · Gut · doi:10.1136/gutjnl-2012-303207 · Cited by 1,004 · see citing works
Self-citationImmunological aspects of intestinal mucus and mucins
Johansson, M. E. V., & Hansson, G. C. (2016) · Nature Reviews Immunology · doi:10.1038/nri.2016.88 · Cited by 1,007 · see citing works
Self-citationThe intestinal epithelium: central coordinator of mucosal immunity
Allaire, J. M., Crowley, S. M., Law, H. T., Chang, S.-Y., Ko, H.-J., & Vallance, B. A. (2018) · Trends in Immunology · doi:10.1016/j.it.2018.04.002 · Cited by 933 · see citing works
Indoleacrylic Acid Produced by Commensal Peptostreptococcus Species Suppresses Inflammation
Wlodarska, M., Luo, C., Kolde, R., d'Hennezel, E. B., Annand, J. W., Heim, C. E., Krastel, P., Schmitt, E. K., Omar, A. S., Creasey, E. A., et al. (2017) · Cell Host & Microbe · doi:10.1016/j.chom.2017.06.007 · Cited by 890 · see citing works
Colonic epithelial cell diversity in health and inflammatory bowel disease
Parikh, K., Antanaviciute, A., Fawkner-Corbett, D., Jagielowicz, M., Aulicino, A., Lagerholm, B. C., Davis, S. A., Kinchen, J. W., Chen, H. H., Alham, N. K., et al. (2019) · Nature · doi:10.1038/s41586-019-0992-y · Cited by 859 · see citing works
Microbiota and Host Nutrition across Plant and Animal Kingdoms
Hacquard, S., Garrido-Oter, R., González, A., Spaepen, S., Ackermann, G., Lebeis, S., McHardy, A. C., Dangl, J. L., Knight, R., Ley, R., et al. (2015) · Cell Host & Microbe · doi:10.1016/j.chom.2015.04.009 · Cited by 779 · see citing works
Wrzosek, L., Miquel, S., Noordine, M.-L., Bouet, S., Curt, M. J.-C., Robert, V., Philippe, C., Bridonneau, C., Cherbuy, C., Masselot, C. R., et al. (2013) · BMC Biology · doi:10.1186/1741-7007-11-61 · Cited by 807 · see citing works
The composition of the gut microbiota shapes the colon mucus barrier
Jakobsson, H. E., Rodríguez‐Piñeiro, A. M., Schütte, A., Ermund, A., Boysen, P., Bemark, M., Sommer, F., Bäckhed, F., Hansson, G. C., & Johansson, M. E. (2015) · The EMBO Reports · doi:10.15252/embr.201439263 · Cited by 700 · see citing works
“Failure of this protective barrier to separate bacteria from the epithelium is observed in a number of murine colitis models [15,17].”
Self-citationThe role of goblet cells and mucus in intestinal homeostasis
Gustafsson, J. K., & Johansson, M. (2022) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-022-00675-x · Cited by 698 · see citing works
Self-citationLeaky Gut As a Danger Signal for Autoimmune Diseases
Mu, Q., Kirby, J. L., Reilly, C. M., & Luo, X. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00598 · Cited by 618 · see citing works
A sentinel goblet cell guards the colonic crypt by triggering Nlrp6-dependent Muc2 secretion
Birchenough, G. M. H., Nyström, E. E. L., Johansson, M. E. V., & Hansson, G. C. (2016) · Science · doi:10.1126/science.aaf7419 · Cited by 568 · see citing works
Self-citationKang, C.-S., Ban, M., Choi, E.-J., Moon, H.-G., Jeon, J.-S., Kim, D.-K., Park, S.-K., Jeon, S. G., Roh, T.-Y., Myung, S.-J., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0076520 · Cited by 543 · see citing works
Lyte, M. (2011) · BioEssays · doi:10.1002/bies.201100024 · Cited by 549 · see citing works
Gut barrier disruption and chronic disease
Martel, J., Chang, S.-H., Ko, Y.-F., Hwang, T.-L., Young, J. D., & Ojcius, D. M. (2022) · Trends in Endocrinology & Metabolism · doi:10.1016/j.tem.2022.01.002 · Cited by 514 · see citing works
Role of mucus layers in gut infection and inflammation
Hansson, G. C. (2011) · Current Opinion in Microbiology · doi:10.1016/j.mib.2011.11.002 · Cited by 473 · see citing works
Self-citationGrondin, J. A., Kwon, Y. H., Far, P. M., Haq, S., & Khan, W. I. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.02054 · Cited by 468 · see citing works
The microbiome and gut homeostasis
Lee, J., Tsolis, R. M., & Bäumler, A. J. (2022) · Science · doi:10.1126/science.abp9960 · Cited by 430 · see citing works
Touchefeu, Y., Montassier, E., Nieman, K. M., Gastinne, T., Potel, G., Varannes, S. B. D., Vacon, F. L., & Cochetiere, M. F. D. L. (2014) · Alimentary Pharmacology & Therapeutics · doi:10.1111/apt.12878 · Cited by 427 · see citing works
Bile acids as modulators of gut microbiota composition and function
Larabi, A. B., Masson, H. L. P., & Bäumler, A. J. (2023) · Gut Microbes · doi:10.1080/19490976.2023.2172671 · Cited by 420 · see citing works
Commensal bacteria-dependent indole production enhances epithelial barrier function in the colon
Shimada, Y., Kinoshita, M., Harada, K., Mizutani, M., Masahata, K., Kayama, H., & Takeda, K. (2013) · PLoS ONE · doi:10.1371/journal.pone.0080604 · Cited by 404 · see citing works
Ermund, A., Schutte, A. H., Johansson, M., Gustafsson, J. K., & Hansson, G. C. (2013) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00046.2013 · Cited by 392 · see citing works
Self-citationMucin-type O-glycans and their roles in intestinal homeostasis
Bergstrom, K. S. B., & Xia, L. (2013) · Glycobiology · doi:10.1093/glycob/cwt045 · Cited by 360 · see citing works
Importance and regulation of the colonic mucus barrier in a mouse model of colitis
Petersson, J., Schreiber, O., Hansson, G. C., Gendler, S. J., Velcich, A., Lundberg, J. O., Roos, S., Holm, L., & Phillipson, M. (2010) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00422.2010 · Cited by 384 · see citing works
Self-citationLoss of intestinal core 1–derived O-glycans causes spontaneous colitis in mice
Fu, J., Wei, B., Wen, T., Johansson, M. E. V., Liu, X., Bradford, E., Thomsson, K. A., McGee, S., Mansour, L., Tong, M., et al. (2011) · Journal of Clinical Investigation · doi:10.1172/jci45538 · Cited by 366 · see citing works
Self-citationAn intercrypt subpopulation of goblet cells is essential for colonic mucus barrier function
Nyström, E. E. L., Martínez‐Abad, B., Arike, L., Birchenough, G. M. H., Nonnecke, E. B., Castillo, P. A., Svensson, F. R., Bevins, C. L., Hansson, G. C., & Johansson, M. (2021) · Science · doi:10.1126/science.abb1590 · Cited by 349 · see citing works
Self-citationRausch, P., Rehman, A., Künzel, S., Häsler, R., Ott, S. J., Schreiber, S., Rosenstiel, P. C., Franke, A., & Baines, J. F. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1106408108 · Cited by 348 · see citing works
d’Enfert, C., Kaune, A.-K., Alaban, L. R., Chakraborty, S., Cole, N. L., Delavy, M., Kosmala, D., Marsaux, B., Fróis-Martins, R., Morelli, M., et al. (2020) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuaa060 · Cited by 351 · see citing works
Gustafsson, J. K., Ermund, A., Ambort, D., Johansson, M., Nilsson, H. E., Thorell, K., Hebert, H., Sjövall, H., & Hansson, G. C. (2012) · The Journal of Experimental Medicine · doi:10.1084/jem.20120562 · Cited by 345 · see citing works
Self-citationYao, D., Dong, M., Dai, C., & Wu, S. (2019) · Inflammatory Bowel Diseases · doi:10.1093/ibd/izz149 · Cited by 337 · see citing works
Berry, D., Schwab, C., Milinovich, G. J., Reichert, J., Mahfoudh, K. B., Decker, T., Engel, M., Hai, B., Hainzl, E., Heider, S., et al. (2012) · The ISME Journal · doi:10.1038/ismej.2012.39 · Cited by 333 · see citing works
The gut microbiota and its biogeography
McCallum, G., & Tropini, C. (2023) · Nature Reviews Microbiology · doi:10.1038/s41579-023-00969-0 · Cited by 342 · see citing works
Maisel, K., Ensign, L. M., Reddy, M., Cone, R. A., & Hanes, J. S. (2014) · Journal of Controlled Release · doi:10.1016/j.jconrel.2014.10.026 · Cited by 320 · see citing works
Role of the microbiota in inflammatory bowel diseases
Nagalingam, N. A., & Lynch, S. V. (2012) · Inflammatory Bowel Diseases · doi:10.1002/ibd.21866 · Cited by 315 · see citing works
Goblet cells: multifaceted players in immunity at mucosal surfaces
Knoop, K. A., & Newberry, R. D. (2018) · Mucosal Immunology · doi:10.1038/s41385-018-0039-y · Cited by 316 · see citing works
Engineering bacterial thiosulfate and tetrathionate sensors for detecting gut inflammation
Daeffler, K. N.-M., Galley, J. D., Sheth, R. U., Ortiz-Velez, L., Bibb, C. O., Shroyer, N. F., Britton, R. A., & Tabor, J. J. (2017) · Molecular Systems Biology · doi:10.15252/msb.20167416 · Cited by 302 · see citing works
Jang, Y. J., Kim, W.-K., Han, D. H., Lee, K., & Ko, G. (2019) · Gut Microbes · doi:10.1080/19490976.2019.1589281 · Cited by 301 · see citing works
Sulfide as a Mucus Barrier-Breaker in Inflammatory Bowel Disease?
Ijssennagger, N., van der Meer, R., & van Mil, S. W. C. (2016) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2016.01.002 · Cited by 297 · see citing works
The host selects mucosal and luminal associations of coevolved gut microorganisms: a novel concept
den Abbeele, P. V., de Wiele, T. V., Verstraete, W., & Possemiers, S. (2011) · FEMS Microbiology Reviews · doi:10.1111/j.1574-6976.2011.00270.x · Cited by 263 · see citing works
Unveiling Colitis: A Journey through the Dextran Sodium Sulfate-induced Model
Yang, C., & Merlin, D. (2023) · Inflammatory Bowel Diseases · doi:10.1093/ibd/izad312 · Cited by 253 · see citing works
Gustafsson, J. K., Ermund, A., Johansson, M., Schutte, A. H., Hansson, G. C., & Sjövall, H. (2011) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00405.2011 · Cited by 251 · see citing works
Self-citationMicrobiota-mediated inflammation and antimicrobial defense in the intestine
Caballero, S., & Pamer, E. G. (2015) · Annual Review of Immunology · doi:10.1146/annurev-immunol-032713-120238 · Cited by 238 · see citing works
Sontheimer-Phelps, A., Chou, D. B., Tovaglieri, A., Ferrante, T. C., Duckworth, T., Fadel, C., Frismantas, V., Sutherland, A. D., Jalili-Firoozinezhad, S., Kasendra, M., et al. (2020) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2019.11.008 · Cited by 239 · see citing works
Subramanian, D. A., Langer, R., & Traverso, G. (2022) · Journal of Nanobiotechnology · doi:10.1186/s12951-022-01539-x · Cited by 247 · see citing works
Innate immune signalling at the intestinal epithelium in homeostasis and disease
Pott, J., & Hornef, M. W. (2012) · EMBO Reports · doi:10.1038/embor.2012.96 · Cited by 227 · see citing works
Identification of Potential Biomarkers for Gut Barrier Failure in Broiler Chickens
Chen, J., Téllez‐Isaías, G., Richards, J. D., & Escobar, J. (2015) · Frontiers in Veterinary Science · doi:10.3389/fvets.2015.00014 · Cited by 222 · see citing works
Loss of gut barrier integrity triggers activation of islet-reactive T cells and autoimmune diabetes
Sorini, C., Cosorich, I., Conte, M. L., Giorgi, L. D., Facciotti, F., Lucianò, R., Rocchi, M., Ferrarese, R., Sanvito, F., Canducci, F., et al. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1814558116 · Cited by 220 · see citing works
CFTR, Mucins, and Mucus Obstruction in Cystic FibrosisPreprint
Kreda, S. M., Davis, C. W., & Rose, M. C. (2012) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a009589 · Cited by 220 · see citing works
The microbiota programs DNA methylation to control intestinal homeostasis and inflammation
Ansari, I., Raddatz, G., Gutekunst, J., Ridnik, M., Cohen, D., Abu-Remaileh, M., Tuganbaev, T., Shapiro, H., Pikarsky, E., Elinav, E., et al. (2020) · Nature Microbiology · doi:10.1038/s41564-019-0659-3 · Cited by 202 · see citing works
Scaldaferri, F., Pizzoferrato, M., Gerardi, V., Lopetuso, L. R., & Gasbarrini, A. (2012) · Journal of Clinical Gastroenterology · doi:10.1097/mcg.0b013e31826ae849 · Cited by 203 · see citing works
Schwab, C., Berry, D., Rauch, I., Rennisch, I. M., Ramesmayer, J., Hainzl, E., Heider, S., Decker, T., Kenner, L., Müller, M. M., et al. (2014) · The ISME Journal · doi:10.1038/ismej.2013.223 · Cited by 193 · see citing works
Commensal microbiota induces colonic barrier structure and functions that contribute to homeostasis
Hayes, C. L., Dong, J., Galipeau, H. J., Jury, J., McCarville, J. L., Huang, X., Wang, X.-Y., Naidoo, A., Anbazhagan, A. N., Libertucci, J., et al. (2018) · Scientific Reports · doi:10.1038/s41598-018-32366-6 · Cited by 190 · see citing works
Johansson, M., & Hansson, G. C. (2011) · Methods in molecular biology · doi:10.1007/978-1-61779-513-8_13 · Cited by 188 · see citing works
Self-citationKaiser, P., Diard, M., Stecher, B., & Hardt, W. (2011) · Immunological Reviews · doi:10.1111/j.1600-065x.2011.01070.x · Cited by 181 · see citing works
Ahl, D., Liu, H., Schreiber, O., Roos, S., Phillipson, M., & Holm, L. (2016) · Acta Physiologica · doi:10.1111/apha.12695 · Cited by 182 · see citing works
Self-citationMucosal Barrier, Bacteria and Inflammatory Bowel Disease: Possibilities for Therapy
Merga, Y., Campbell, B. J., & Rhodes, J. M. (2014) · Digestive Diseases · doi:10.1159/000358156 · Cited by 180 · see citing works
Wang, A., Keita, Å. V., Phan, V., McKay, C. M., Schoultz, I., Lee, J., Murphy, M. P., Fernando, M., Ronaghan, N. J., Balce, D. R., et al. (2014) · American Journal Of Pathology · doi:10.1016/j.ajpath.2014.05.019 · Cited by 177 · see citing works
Experimental models to study intestinal microbes–mucus interactions in health and disease
Etienne‐Mesmin, L., Chassaing, B., Desvaux, M., Paepe, K. D., Gresse, R., Sauvaitre, T., Forano, É., de Wiele, T. V., Schüller, S., Juge, N., et al. (2019) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuz013 · Cited by 178 · see citing works
A slippery slope: On the origin, role and physiology of mucus
Taherali, F., Varum, F., & Basit, A. W. (2017) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2017.10.014 · Cited by 171 · see citing works
Human herpes simplex virus: Life cycle and development of inhibitors
Kukhanova, M. K., Korovina, A. N., & Kochetkov, S. N. (2014) · Biochemistry (Moscow) · doi:10.1134/s0006297914130124 · Cited by 166 · see citing works
The Role of Dietary Nutrients in Inflammatory Bowel Disease
Sugihara, K., Morhardt, T. L., & Kamada, N. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2018.03183 · Cited by 166 · see citing works
Toll-Like Receptor–Gut Microbiota Interactions: Perturb at Your Own Risk!
Carvalho, F. A., Aitken, J. D., Vijay–Kumar, M., & Gewirtz, A. T. (2011) · Annual Review of Physiology · doi:10.1146/annurev-physiol-020911-153330 · Cited by 164 · see citing works
The role of glycosylation in IBD
Τheodoratou, E., Campbell, H. J., Ventham, N. T., Kolarich, D., Pučić‐Baković, M., Zoldoš, V., Fernandes, D. L., Pemberton, I. K., Rudan, I., Kennedy, N. A., et al. (2014) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2014.78 · Cited by 159 · see citing works
Kanai∥, T., Mikami, Y., & Hayashi, A. (2015) · Journal of Gastroenterology · doi:10.1007/s00535-015-1084-x · Cited by 159 · see citing works
Intestinal microbiota: A source of novel biomarkers in inflammatory bowel diseases?
Berry, D., & Reinisch, W. (2013) · Best Practice & Research Clinical Gastroenterology · doi:10.1016/j.bpg.2013.03.005 · Cited by 154 · see citing works
Allen, J. M., Mailing, L. J., Cohrs, J., Salmonson, C., Fryer, J. D., Nehra, V., Hale, V. L., Kashyap, P., White, B. A., & Woods, J. A. (2018) · Gut Microbes · doi:10.1080/19490976.2017.1372077 · Cited by 152 · see citing works
Mucin Function in Inflammatory Bowel Disease
Boltin, D., Perets, T. T., Vilkin, A., & Niv, Y. (2012) · Journal of Clinical Gastroenterology · doi:10.1097/mcg.0b013e3182688e73 · Cited by 151 · see citing works
Sommer, F., Adam, N., Johansson, M., Xia, L., Hansson, G. C., & Bäckhed, F. (2014) · PLoS ONE · doi:10.1371/journal.pone.0085254 · Cited by 150 · see citing works
Self-citationFurter, M., Sellin, M. E., Hansson, G. C., & Hardt, W. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.04.106 · Cited by 149 · see citing works
Self-citationMucus Layers in Inflammatory Bowel Disease
Johansson, M. (2014) · Inflammatory Bowel Diseases · doi:10.1097/mib.0000000000000117 · Cited by 148 · see citing works
Self-citationAntimicrobial peptides and the enteric mucus layer act in concert to protect the intestinal mucosa
Dupont, A., Heinbockel, L., Brandenburg, K., & Hornef, M. W. (2014) · Gut Microbes · doi:10.4161/19490976.2014.972238 · Cited by 141 · see citing works
Sheng, Y., Lourie, R., Lindén, S. K., Jeffery, P. L., Roche, D., Tran, T. V., Png, C. W., Waterhouse, N. J., SUTTON, P. R. N., Florin, T. H., et al. (2011) · Gut · doi:10.1136/gut.2011.239194 · Cited by 140 · see citing works
Role of the intestinal microbiome, intestinal barrier and psychobiotics in depression
Trzeciak, P., & Herbet, M. (2021) · Nutrients · doi:10.3390/nu13030927 · Cited by 139 · see citing works
The Anti-inflammatory Effects of Dietary Anthocyanins against Ulcerative Colitis
Li, S., Wu, B., Fu, W., & Reddivari, L. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20102588 · Cited by 138 · see citing works
The Nlrp6 inflammasome is not required for baseline colonic inner mucus layer formation or function
Volk, J. K., Nyström, E. E. L., van der Post, S., Martínez‐Abad, B., Schroeder, B. O., Johansson, Å., Svensson, F. R., Jäverfelt, S., Johansson, M., Hansson, G. C., et al. (2019) · The Journal of Experimental Medicine · doi:10.1084/jem.20190679 · Cited by 128 · see citing works
Self-citationSommer, F., & Bäckhed, F. (2014) · Mucosal Immunology · doi:10.1038/mi.2014.74 · Cited by 120 · see citing works
Johansson, M., & Hansson, G. C. (2013) · Digestive Diseases · doi:10.1159/000354683 · Cited by 119 · see citing works
Self-citationMonk, J. M., Lepp, D., Zhang, C. P., Wu, W., Zarepoor, L., Lu, J. T., Pauls, K. P., Tsao, R., Wood, G. A., Robinson, L. E., et al. (2015) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2015.10.014 · Cited by 114 · see citing works
Morampudi, V., Dalwadi, U., Bhinder, G., Sham, H. P., Gill, S. K., Chan, J., Bergstrom, K., Huang, T., Ma, C., Jacobson, K., et al. (2016) · Mucosal Immunology · doi:10.1038/mi.2015.140 · Cited by 114 · see citing works
Round, A. N., Rigby, N. M., la Torre, A. G.-D., Macierzanka, A., Mills, E. N. C., & Mackie, A. R. (2012) · Biomacromolecules · doi:10.1021/bm301024x · Cited by 112 · see citing works
Grootjans, J., Hundscheid, I. H. R., Lenaerts, K., Boonen, B., Renes, I. B., Verheyen, F., Dejong, C. H. C., MEYENFELDT, M. F. V., Beets, G. L., & Buurman, W. A. (2012) · Gut · doi:10.1136/gutjnl-2011-301956 · Cited by 109 · see citing works
Neonatal Immune Adaptation of the Gut and Its Role during Infections
Tourneur, E., & Chassin, C. (2013) · Clinical and Developmental Immunology · doi:10.1155/2013/270301 · Cited by 110 · see citing works
The Effect of Bacterial Infections, Probiotics and Zonulin on Intestinal Barrier Integrity
Serek, P., & Oleksy-Wawrzyniak, M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222111359 · Cited by 113 · see citing works
Induction of gut IgA production through T cell‐dependent and T cell‐independent pathways
Bemark, M., Boysen, P., & Lycke, N. Y. (2012) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2011.06378.x · Cited by 107 · see citing works
Lock, J. Y., Carlson, T. L., Wang, C.-M., Chen, A., & Carrier, R. L. (2018) · Scientific Reports · doi:10.1038/s41598-018-27957-2 · Cited by 105 · see citing works
Nyström, E. E. L., Birchenough, G. M. H., van der Post, S., Arike, L., Gruber, A. D., Hansson, G. C., & Johansson, M. (2018) · EBioMedicine · doi:10.1016/j.ebiom.2018.05.031 · Cited by 102 · see citing works
Self-citationThomsson, K. A., Holmén‐Larsson, J., Ångström, J., Johansson, M., Xia, L., & Hansson, G. C. (2012) · Glycobiology · doi:10.1093/glycob/cws083 · Cited by 101 · see citing works
Self-citationRingseis, R., & Eder, K. (2022) · Journal of Animal Science and Biotechnology/Journal of animal science and biotechnology · doi:10.1186/s40104-022-00783-3 · Cited by 96 · see citing works
Deregulation of intestinal anti-microbial defense by the dietary additive, maltodextrin
Nickerson, K. P., Chanin, R. B., & McDonald, C. (2015) · Gut Microbes · doi:10.1080/19490976.2015.1005477 · Cited by 98 · see citing works
Hoffmann, W. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21124535 · Cited by 94 · see citing works
Alves, N. D. O., Dalmasso, G., Nikitina, D., Vaysse, A., Ruez, R., Ledoux, L., Pédron, T., Bergsten, E., Boulard, O., Autier, L., et al. (2024) · Gut Microbes · doi:10.1080/19490976.2024.2320291 · Cited by 95 · see citing works
Therapeutic Potential to Modify the Mucus Barrier in Inflammatory Bowel Disease
Sun, J., Shen, X., Li, Y., Guo, Z., Zhu, W., Zuo, L., Zhao, J., Gu, L., Gong, J., & Li, J. (2016) · Nutrients · doi:10.3390/nu8010044 · Cited by 92 · see citing works
A sticky end for gastrointestinal helminths; the role of the mucus barrier
Sharpe, C., Thornton, D. J., & Grencis, R. K. (2018) · Parasite Immunology · doi:10.1111/pim.12517 · Cited by 92 · see citing works
Noninvasive assessment of gut function using transcriptional recording sentinel cells
Schmidt, F., Zimmermann, J., Tanna, T., Farouni, R., Conway, T., Macpherson, A. J., & Platt, R. J. (2022) · Science · doi:10.1126/science.abm6038 · Cited by 92 · see citing works
Xiao, F., Juric, M., Li, J., Riederer, B., Yeruva, S., Singh, A. K., Zheng, L., Glage, S., Kollias, G. A., Dudeja, P. K., et al. (2011) · Inflammatory Bowel Diseases · doi:10.1002/ibd.21744 · Cited by 91 · see citing works
Bacterial Oncogenesis in the Colon
Dejea, C. M., Wick, E., & Sears, C. L. (2013) · Future Microbiology · doi:10.2217/fmb.13.17 · Cited by 90 · see citing works
Exploring the influence of the gut microbiota and probiotics on health: a symposium report
Thomas, L. V., Ockhuizen, T., & Suzuki, K. (2014) · British Journal Of Nutrition · doi:10.1017/s0007114514001275 · Cited by 89 · see citing works
AGR2, an Endoplasmic Reticulum Protein, Is Secreted into the Gastrointestinal Mucus
Bergström, J. H., Berg, K. A., Rodríguez-Piñeiro, A. M., Stecher, B., Johansson, M., & Hansson, G. C. (2014) · PLoS ONE · doi:10.1371/journal.pone.0104186 · Cited by 88 · see citing works
Self-citation
- Authors
- Johansson, M. E. V., Gustafsson, J. K., Sjöberg, K. E., Petersson, J., Holm, L., Sjövall, H., & Hansson, G. C.
- Affiliations
- University of Gothenburg (SE)
- Uppsala University (SE)
- Corresponding author
- Hansson, Gunnar C.
- Venue
- PLoS ONE
- Publisher
- Public Library of Science (PLoS)
- Published
- 2010-08-18
- Volume
- 5
- Issue
- 8
- Pages
- e12238
- ISSN
- 1932-6203 (ISSN-L)
- PMC
- PMC2923597
- OpenAlex
- W1977781139
- Cited by
- 368
- References
- 31
- Citations by year
- 2026: 12 · 2025: 19 · 2024: 18 · 2023: 26 · 2022: 27 · 2021: 17 · 2020: 17 · 2019: 28 · 2018: 19 · 2017: 22 · 2016: 24 · 2015: 22 · 2014: 30 · 2013: 39 · 2012: 21
- FWCI
- 15.49
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- PLoS ONE (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Figshare (submittedVersion, cc-by)
- Funders
- Swedish Cancer Foundation
- Stiftelsen för Strategisk Forskning
- Knut och Alice Wallenbergs Stiftelse (KAW2007.0118)
- Vetenskapsrådet (21027, 342–2004-4434)
- Göteborgs Universitet
- National Institute of Allergy and Infectious Diseases (U01AI095473)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Inflammatory Bowel Disease
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Health Sciences › Medicine › Gastroenterology › Gastrointestinal motility and disorders
- Keywords
- mucus permeability, ulcerative colitis, MUC2, commensal bacteria, colonic epithelium, pathogenesis of inflammation
- MeSH terms
- Adult, Aged, Animals, Bacteria, Colitis, Colon, Disease Models, Animal, Female, Humans, Intestinal Mucosa, Male, Mice, Inbred C57BL, Permeability, Time Factors, Dextran Sulfate, Mice
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review