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Tryptophan Dietary Impacts Gut Barrier and Metabolic Diseases
Open accessAbstract
The intestine has a major role in the digestion and absorption of nutrients, and gut barrier is the first defense line against harmful pathogens. Alteration of the intestinal barrier is associated with enhanced intestinal permeability and development of numerous pathological diseases including gastrointestinal and cardiometabolic diseases. Among the metabolites that play an important role within intestinal health, L Tryptophan (Trp) is one of the nine essential amino acids supplied by diet, whose metabolism appears as a key modulator of gut microbiota, with major impacts on physiological, and pathological pathways. Recently, emerging evidence showed that the Trp catabolism through one major enzyme indoleamine 2,3-dioxygenase 1 (IDO1) expressed by the host affects Trp metabolism by gut microbiota to generate indole metabolites, thereby altering gut function and health in mice and humans. In this mini review, I summarize the most recent advances concerning the role of Trp metabolism in host-microbiota cross-talk in health, and metabolic diseases. This novel aspect of IDO1 function in intestine will better explain its complex roles in a broad range of disease states where the gut function affects local as well as systemic health, and will open new therapeutic strategies.
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“the indole pathway is completely microbe dependent, as only certain microbes possess the enzyme tryptophanase required for their production from Trp [34].”
From Role of diet and its effects on the gut microbiome in the pathophysiology of mental disorders (2022) · cites this paper as [34]
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Cites
Cani, P. D., Bibiloni, R., Knauf, C., Waget, A., Neyrinck, A. M., Delzenne, N. M., & Burcelin, R. (2008) · Diabetes · doi:10.2337/db07-1403 · Cited by 4,819
Metabolomics analysis reveals large effects of gut microflora on mammalian blood metabolites
Wikoff, W. R., Anfora, A. T., Liu, J., Schultz, P. G., Lesley, S. A., Peters, E. C., & Siuzdak, G. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0812874106 · Cited by 2,677
Zelante, T., Iannitti, R. G., Cunha, C., De Luca, A., Giovannini, G., Pieraccini, G., Zecchi, R., D’Angelo, C., Massi-Benedetti, C., Fallarino, F., et al. (2013) · Immunity · doi:10.1016/j.immuni.2013.08.003 · Cited by 2,614
Ido expression by dendritic cells: tolerance and tryptophan catabolism
Mellor, A. L., & Munn, D. H. (2004) · Nature Reviews Immunology · doi:10.1038/nri1457 · Cited by 2,341
Clarke, G., Grenham, S., Scully, P., Fitzgerald, P., Moloney, R. D., Shanahan, F., Dinan, T. G., & Cryan, J. F. (2013) · Molecular Psychiatry · doi:10.1038/mp.2012.77 · Cited by 1,893
Gut microbiota in cardiovascular health and disease
Tang, W. H. W., Kitai, T., & Hazen, S. L. (2017) · Circulation Research · doi:10.1161/circresaha.117.309715 · Cited by 1,670
Lamas, B., Richard, M. L., Leducq, V., Pham, H.-P., Michel, M.-L., Da Costa, G., Bridonneau, C., Jegou, S., Hoffmann, T. W., Natividad, J. M., et al. (2016) · Nature Medicine · doi:10.1038/nm.4102 · Cited by 1,482
Self-citationSignals from the gut microbiota to distant organs in physiology and disease
Schroeder, B. O., & Bäckhed, F. (2016) · Nature Medicine · doi:10.1038/nm.4185 · Cited by 1,409
Impact of the Gut Microbiota on Intestinal Immunity Mediated by Tryptophan Metabolism
Gao, J., Xu, K., Liu, H., Liu, G., Bai, M., Peng, C., Li, T., & Yin, Y. (2018) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2018.00013 · Cited by 1,357
ACE2 links amino acid malnutrition to microbial ecology and intestinal inflammation
Hashimoto, T., Perlot, T., Rehman, A., Trichereau, J., Ishiguro, H., Paolino, M., Sigl, V., Hanada, T., Hanada, R., Lipinski, S., et al. (2012) · Nature · doi:10.1038/nature11228 · Cited by 1,271
IDO in the Tumor Microenvironment: Inflammation, Counter-Regulation, and Tolerance
Munn, D. H., & Mellor, A. L. (2016) · Trends in Immunology · doi:10.1016/j.it.2016.01.002 · Cited by 1,081
Venkatesh, M., Mukherjee, S., Wang, H., Li, H., Sun, K., Benechet, A. P., Qiu, Z., Maher, L., Redinbo, M. R., Phillips, R. S., et al. (2014) · Immunity · doi:10.1016/j.immuni.2014.06.014 · Cited by 1,066
Regulation of the immune response by the aryl hydrocarbon receptor
Gutiérrez-Vázquez, C., & Quintana, F. J. (2018) · Immunity · doi:10.1016/j.immuni.2017.12.012 · Cited by 985
Hyperglycemia drives intestinal barrier dysfunction and risk for enteric infection
Thaiss, C. A., Levy, M., Grosheva, I., Zheng, D., Soffer, E., Blacher, E., Braverman, S., Tengeler, A. C., Barak, O., Elazar, M., et al. (2018) · Science · doi:10.1126/science.aar3318 · Cited by 942
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 918
Protective Role of Interleukin-10 in Atherosclerosis
Mallat, Z., Besnard, S., Duriez, M., Deleuze, V., Emmanuel, F., Bureau, M. F., Soubrier, F., Esposito, B., Duez, H., Fiévet, C., et al. (1999) · Circulation Research · doi:10.1161/01.res.85.8.e17 · Cited by 846
Aryl hydrocarbon receptor control of a disease tolerance defence pathway
Bessede, A., Gargaro, M., Pallotta, M. T., Matino, D., Servillo, G., Brunacci, C., Bicciato, S., Mazza, E. M. C., Macchiarulo, A., Vacca, C., et al. (2014) · Nature · doi:10.1038/nature13323 · Cited by 693
Natividad, J. M., Agus, A., Planchais, J., Lamas, B., Jarry, A. C., Martin, R., Michel, M.-L., Chong-Nguyen, C., Roussel, R., Straube, M., et al. (2018) · Cell Metabolism · doi:10.1016/j.cmet.2018.07.001 · Cited by 642
Causes, Characteristics, and Consequences of Metabolically Unhealthy Normal Weight in Humans
Stefan, N., Schick, F., & Häring, H.-U. (2017) · Cell Metabolism · doi:10.1016/j.cmet.2017.07.008 · Cited by 575 · cited 1×
“The prevalence of Western diet-induced metabolic syndrome (MetS) is booming, affecting more than 2 billion people worldwide and accounting for at least 3 million deaths per year (1).”
BackgroundCaleyachetty, R., Thomas, G. N., Toulis, K. A., Mohammed, N., Gokhale, K. M., Balachandran, K., & Nirantharakumar, K. (2017) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2017.07.763 · Cited by 574
Bacterial metabolite indole modulates incretin secretion from intestinal enteroendocrine L cells
Chimerel, C., Emery, E., Summers, D. K., Keyser, U., Gribble, F. M., & Reimann, F. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.10.032 · Cited by 548 · cited 1×
“related to their local effects on intestine through promoting IL-22 production and/or the stimulation of enteroendocrine L cells to produce glucagon-like peptide-1 (GLP-1), an incretin stimulating the secretion of insulin by pancreatic β cells (47, 55).”
BackgroundInterleukin-22 alleviates metabolic disorders and restores mucosal immunity in diabetes
Wang, X., Ota, N., Manzanillo, P. S., Kates, L., Zavala‐Solorio, J., Eidenschenk, C., Zhang, J., Lesch, J., Lee, W. P., Ross, J., et al. (2014) · Nature · doi:10.1038/nature13564 · Cited by 512
Crane, J. D., Palanivel, R., Mottillo, E. P., Bujak, A. L., Wang, H., Ford, R. J., Collins, A., Blümer, R. M. E., Fullerton, M. D., Yabut, J. M., et al. (2014) · Nature Medicine · doi:10.1038/nm.3766 · Cited by 509
Kynurenine is an endothelium-derived relaxing factor produced during inflammation
Wang, Y., Liu, H., McKenzie, G. A., Witting, P. K., Stasch, J., Hahn, M. G., Changsirivathanathamrong, D., Wu, B. J., Ball, H. J., Thomas, S. R., et al. (2010) · Nature Medicine · doi:10.1038/nm.2092 · Cited by 446
Microbial modulation of cardiovascular disease
Brown, J. M., & Hazen, S. L. (2018) · Nature Reviews Microbiology · doi:10.1038/nrmicro.2017.149 · Cited by 440
Inhibitors of indoleamine-2,3-dioxygenase for cancer therapy: can we see the wood for the trees?
Löb, S., Königsrainer, A., Rammensee, H., Opelz, G., & Terness, P. (2009) · Nature reviews. Cancer · doi:10.1038/nrc2639 · Cited by 421
Genetic deficiency of indoleamine 2,3-dioxygenase promotes gut microbiota-mediated metabolic health
Laurans, L., Venteclef, N., Haddad, Y., Chajadine, M., Alzaïd, F., Metghalchi, S., Sovran, B., Denis, R., Dairou, J., Cardellini, M., et al. (2018) · Nature Medicine · doi:10.1038/s41591-018-0060-4 · Cited by 315
Self-citationKynurenic Acid and Gpr35 Regulate Adipose Tissue Energy Homeostasis and Inflammation
Agudelo, L. Z., Ferreira, D. M. S., Červenka, I., Bryzgalova, G., Dadvar, S., Jannig, P. R., Pettersson-Klein, A. T., Lakshmikanth, T., Sustarsic, E. G., Porsmyr‐Palmertz, M., et al. (2018) · Cell Metabolism · doi:10.1016/j.cmet.2018.01.004 · Cited by 311
Determinants of colonic barrier function in inflammatory bowel disease and potential therapeutics
Hering, N. A., Fromm, M., & Schulzke, J. (2012) · The Journal of Physiology · doi:10.1113/jphysiol.2011.224568 · Cited by 279
Favennec, M., Hennart, B., Caiazzo, R., Leloire, A., Yengo, L., Verbanck, M., Arredouani, A., Marre, M., Pigeyre, M., Bessède, A., et al. (2015) · Obesity · doi:10.1002/oby.21199 · Cited by 261
Differential vulnerability of central neurons of the rat to quinolinic acid
Schwarcz, R., & Köhler, C. (1983) · Neuroscience Letters · doi:10.1016/0304-3940(83)90115-5 · Cited by 239
The gut microbiota metabolite indole alleviates liver inflammation in mice
Beaumont, M., Neyrinck, A. M., Olivares, M., Rodriguez, J., Nédélec, A., Roumain, M., Bindels, L. B., Cani, P. D., Evenepoel, P., Muccioli, G. G., et al. (2018) · The FASEB Journal · doi:10.1096/fj.201800544 · Cited by 214
Fatkhullina, A. R., Peshkova, I. O., Dzutsev, A., Aghayev, T., McCulloch, J. A., Thovarai, V., Badger, J. H., Vats, R., Sundd, P., Tang, H., et al. (2018) · Immunity · doi:10.1016/j.immuni.2018.09.011 · Cited by 186
Martin‐Gallausiaux, C., Larraufie, P., Jarry, A., Béguet-Crespel, F., Marinelli, L., Ledue, F., Reimann, F. M., Blottière, H. M., & Lapaque, N. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02838 · Cited by 174
Chon, S. Y., Hassanain, H. H., & Gupta, S. L. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.29.17247 · Cited by 171
Pedersen, E. R., Tuseth, N., Eussen, S. J. P. M., Ueland, P. M., Strand, E., Svingen, G. F. T., Midttun, Ø., Meyer, K., Mellgren, G., Ulvik, A., et al. (2014) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.114.304674 · Cited by 171
Kynurenic Acid Triggers Firm Arrest of Leukocytes to Vascular Endothelium under Flow Conditions
Barth, M. C., Ahluwalia, N., Anderson, T. J. T., Hardy, G. J., Sinha, S., Alvarez-Cardona, J. A., Pruitt, I. E., Rhee, E. P., Colvin, R. A., & Gerszten, R. E. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.024042 · Cited by 170
Pertovaara, M., Raitala, A., Juonala, M., Lehtimäki, T. J., Huhtala, H., Oja, S. S., Jokinen, E. V., Viikari, J. S. A., Raitakari, O. T., & Hurme, M. (2007) · Clinical & Experimental Immunology · doi:10.1111/j.1365-2249.2007.03325.x · Cited by 148
Metghalchi, S., Ponnuswamy, P., Simon, T., Haddad, Y., Laurans, L., Clément, M., Dalloz, M., Romain, M., Esposito, B., Koropoulis, V., et al. (2015) · Cell Metabolism · doi:10.1016/j.cmet.2015.07.004 · Cited by 143
Self-citationPedersen, E. R., Midttun, Ø., Ueland, P. M., Schartum-Hansen, H., Seifert, R., Igland, J., Nordrehaug, J. E., Ebbing, M., Svingen, G. F. T., Bleie, Ø., et al. (2010) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.110.219329 · Cited by 139
Disturbed Tryptophan Metabolism in Cardiovascular Disease
Mangge, H., Stelzer, I., Reininghaus, E. Z., Weghuber, D., Postolache, T. T., & Fuchs, D. (2014) · Current Medicinal Chemistry · doi:10.2174/0929867321666140304105526 · Cited by 133
IL-17 and Therapeutic Kynurenines in Pathogenic Inflammation to Fungi
Romani, L. R., Zelante, T., LUCA, A. D., Fallarino, F., & Puccetti, P. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.180.8.5157 · Cited by 123
Wolowczuk, I., Hennart, B., Leloire, A., Bessede, A., Soichot, M., Taront, S., Caiazzo, R. J., Raverdy, V., Pigeyre, M., Guillemin, G. J., et al. (2012) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00373.2011 · Cited by 123
Zhang, L., Овчинникова, О. А., Jönsson, A., Lundberg, A. M., Berg, M., Hansson, G. K., & Ketelhuth, D. F. J. (2012) · European Heart Journal · doi:10.1093/eurheartj/ehs175 · Cited by 115
Cole, J. E., Astola, N., Cribbs, A. P., Goddard, M. E., Park, I., Green, P. A., Davies, A. H., Williams, R. O., Feldmann, M., & Monaco, C. G. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1517820112 · Cited by 114
Iyer, S. S., Gensollen, T., Gandhi, A. K., Oh, S. F., Neves, J. F., Collin, F., Lavin, R., Serra, C., Glickman, J. N., de Silva, P. S., et al. (2018) · Cell · doi:10.1016/j.cell.2018.04.037 · Cited by 112
Niinisalo, P., Raitala, A., Pertovaara, M., Oja, S. S., Lehtimäki, T. J., Kähönen, M. A. P., Reunanen, A., Jula, A., Moilanen, L., Kesäniemi, Y. A., et al. (2008) · Scandinavian Journal of Clinical and Laboratory Investigation · doi:10.1080/00365510802245685 · Cited by 107
Polyzos, K. A., Овчинникова, О. А., Berg, M., Baumgartner, R., Agardh, H. E., Pirault, J., Gisterå, A., Assinger, A., Laguna-Fernández, A., Bäck, M., et al. (2015) · Cardiovascular Research · doi:10.1093/cvr/cvv100 · Cited by 102
Brandacher, G., Winkler, C., Aigner, F., Schwelberger, H. G., Schroecksnadel, K., Margreiter, R., Fuchs, D., & Weiss, H. G. (2006) · Obesity Surgery · doi:10.1381/096089206776945066 · Cited by 92
Wang, Q., Ye, D., Song, P., Zhu, H., Okon, I. S., Ding, Y.-N., Chen, H., Liu, D., & Zou, M. (2017) · Circulation · doi:10.1161/circulationaha.117.030972 · Cited by 86
Nakajima, K., Yamashita, T., Kita, T., Takeda, M., Sasaki, N., Kasahara, K., Shinohara, M., Rikitake, Y., Ishida, T., Yokoyama, M., et al. (2011) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.111.229443 · Cited by 84
Indoles - Gut Bacteria Metabolites of Tryptophan with Pharmacotherapeutic Potential
Konopelski, P., & Ufnal, M. (2018) · Current Drug Metabolism · doi:10.2174/1389200219666180427164731 · Cited by 84
Tryptophan Feeding of the IDO1-AhR Axis in Host–Microbial Symbiosis
Zelante, T., Iannitti, R. G., Fallarino, F., Gargaro, M., LUCA, A. D., Moretti, S., Bartoli, A., & Romani, L. R. (2014) · Frontiers in Immunology · doi:10.3389/fimmu.2014.00640 · Cited by 79
Kynurenines as predictors of acute coronary events in the Hordaland Health Study
Eussen, S. J. P. M., Ueland, P. M., Vollset, S. E., Nygard, O. K., Midttun, Ø., Sulo, G., Ulvik, A., Meyer, K., Pedersen, E. R., & Tell, G. S. (2015) · International Journal of Cardiology · doi:10.1016/j.ijcard.2015.03.413 · Cited by 74
Anquetil, F., Mondanelli, G., Gonzalez, N., Calvo, T. R., Zapardiel‐Gonzalo, J., Krogvold, L., Dahl‐Jørgensen, K., den Eynde, B. J. V., Orabona, C., Grohmann, U., et al. (2018) · Diabetes · doi:10.2337/db17-1281 · Cited by 61
Metghalchi, S., Vandestienne, M., Haddad, Y., Esposito, B., Dairou, J., Tedgui, A., Mallat, Z., Potteaux, S., & Taleb, S. (2018) · PLoS ONE · doi:10.1371/journal.pone.0193737 · Cited by 33
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Metadata
- Authors
- Taleb, S.
- Affiliations
- Inserm (FR)
- Corresponding author
- Taleb, Soraya
- ORCID
- Taleb, Soraya
- Venue
- Frontiers in Immunology
- Publisher
- Frontiers Media SA
- Published
- 2019-09-10
- Volume
- 10
- Pages
- 2113-2113
- ISSN
- 1664-3224 (ISSN-L)
- PMC
- PMC6746884
- OpenAlex
- W2969960763
- Cited by
- 236
- References
- 56
- Citations by year
- 2026: 20 · 2025: 55 · 2024: 28 · 2023: 43 · 2022: 32 · 2021: 34 · 2020: 21 · 2019: 1
- FWCI
- 1.94
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Frontiers in Immunology (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Institut National de la Santé et de la Recherche Médicale
- Fondation pour la Recherche Médicale (DEQ20161136699)
- Fondation de France
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Life Sciences › Neuroscience › Biological Psychiatry › Tryptophan and brain disorders
- Life Sciences › Agricultural and Biological Sciences › Animal Science and Zoology › Animal Nutrition and Physiology
- Keywords
- tryptophan metabolism, IDO1, intestinal barrier, intestinal permeability, gut microbiota, indole metabolites, metabolic disorders, cardiometabolic disease, dietary amino acids
- MeSH terms
- Gastrointestinal Microbiome, Host Microbial Interactions, Animals, Diet, Humans, Intestinal Mucosa, Intestines, Metabolic Diseases, Tryptophan, Indoleamine-Pyrrole 2,3,-Dioxygenase, Mice, Microbiota
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