Cited by 167Gut microbiota and healthGastrointestinal motility and disordersInflammatory Bowel Disease

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Role of gut microbiota in intestinal wound healing and barrier function

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Alam, Ashfaqul, Neish, Andrew·2018·Tissue Barriers

DOI 10.1080/21688370.2018.1539595PMC PMC6389125

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Abstract

The mammalian intestine harbors a highly complex and abundant ensemble of bacteria that flourish in a nutrient-rich environment while profoundly influencing many aspects of host biology. The intestine coevolved with its resident microbes in a manner where the mucosa developed a barrier function to segregate the resident microbes from the rest of the body, and yet paradoxically, allowing integration of microbial signals for the host benefit. In this review, we provided a comprehensive overview of why the gut microbiota is key to the efficient development and maintenance of the intestinal barrier. We also highlighted how a destabilized equilibrium between gut microbiota and the host may eventuate in a wide range of intestinal diseases characterized by the disrupted intestinal barrier. Finally, the review delineated how microenvironmental changes in the injured mucosa result in an enrichment of a pro-regenerating consortium of bacteria, which augments mucosal wound repair and restoration of barrier functions.

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Ultra-high-throughput microbial community analysis on the Illumina HiSeq and MiSeq platforms
Caporaso, J. G., Lauber, C. L., Walters, W. A., Berg-Lyons, D., Huntley, J., Fierer, N., Owens, S. M., Betley, J., Fraser, L., Bauer, M., et al. (2012) · The ISME Journal · doi:10.1038/ismej.2012.8 · Cited by 8,839
Changes of Intestinal Functions in Liver Cirrhosis
Fukui, H., & Wiest, R. (2016) · Inflammatory Intestinal Diseases · doi:10.1159/000444436 · Cited by 6,820
The Microbial Metabolites, Short-Chain Fatty Acids, Regulate Colonic T reg Cell Homeostasis
Smith, P. M., Howitt, M. R., Panikov, N., Michaud, M., Gallini, C. A., Bohlooly-Y, M., Glickman, J. N., & Garrett, W. S. (2013) · Science · doi:10.1126/science.1241165 · Cited by 5,413
Host-Bacterial Mutualism in the Human Intestine
Bäckhed, F., Ley, R. E., Sonnenburg, J. L., Peterson, D. A., & Gordon, J. I. (2005) · Science · doi:10.1126/science.1104816 · Cited by 5,277
Induction of Intestinal Th17 Cells by Segmented Filamentous Bacteria
Ivanov, I. I., Atarashi, K., Manel, N., Brodie, E. L., Shima, T., Karaoz, U., Wei, D., Goldfarb, K. C., Santee, C. A., Lynch, S. V., et al. (2009) · Cell · doi:10.1016/j.cell.2009.09.033 · Cited by 4,554
Cross-talk between Akkermansia muciniphila and intestinal epithelium controls diet-induced obesity
Everard, A., Belzer, C., Geurts, L., Ouwerkerk, J. P., Druart, C., Bindels, L. B., Guiot, Y., Derrien, M., Muccioli, G. G., Delzenne, N. M., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1219451110 · Cited by 4,511
Faecalibacterium prausnitzii is an anti-inflammatory commensal bacterium identified by gut microbiota analysis of Crohn disease patients
Sokol, H., Pigneur, B., Watterlot, L., Lakhdari, O., Bermúdez-Humarán, L. G., Gratadoux, J.-J., Blugeon, S., Bridonneau, C., Furet, J.-P., Corthier, G., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804812105 · Cited by 4,413
Reactive oxygen species (ROS) homeostasis and redox regulation in cellular signaling
Ray, P. D., Huang, B.-W., & Tsuji, Y. (2012) · Cellular Signalling · doi:10.1016/j.cellsig.2012.01.008 · Cited by 4,373
Unravelling the pathogenesis of inflammatory bowel disease
Xavier, R. J., & Podolsky, D. K. (2007) · Nature · doi:10.1038/nature06005 · Cited by 4,364
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

Show all 152 references

Research works printed but not linked: 7

10.1038/nature06005.nature06005[pii] · DOI
Lotz MM, 1997, Am J Pathol, 150, 747
Fallingborg J, 1999, Dan Med Bull, 46, 183
10.1016/j.cell.2004.07.002S0092867404006610[pii] · DOI
Abrams GD, 1963, Lab Invest, 12, 355
Dignass AU, 1993, Gastroenterology, 104, A693
Iizuka M, 2002, Gastroenterology, 122, A277

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Additional file 7 of Microbiome diversity declines while distinct expansions of Th17, iNKT, and dendritic cell subpopulations emerge after anastomosis surgery
Vomhof‐DeKrey, E. E., Stover, A. D., & Basson, M. D. (2021) · Figshare · doi:10.6084/m9.figshare.15145811
Additional file 3 of Microbiome diversity declines while distinct expansions of Th17, iNKT, and dendritic cell subpopulations emerge after anastomosis surgery
Vomhof‐DeKrey, E. E., Stover, A. D., & Basson, M. D. (2021) · Figshare · doi:10.6084/m9.figshare.15145799
Additional file 2 of Microbiome diversity declines while distinct expansions of Th17, iNKT, and dendritic cell subpopulations emerge after anastomosis surgery
Vomhof‐DeKrey, E. E., Stover, A. D., & Basson, M. D. (2021) · Figshare · doi:10.6084/m9.figshare.15145796
Additional file 4 of Microbiome diversity declines while distinct expansions of Th17, iNKT, and dendritic cell subpopulations emerge after anastomosis surgery
Vomhof‐DeKrey, E. E., Stover, A. D., & Basson, M. D. (2021) · Figshare · doi:10.6084/m9.figshare.15145802
Additional file 2 of Host metabolome and faecal microbiome shows potential interactions impacted by age and weaning times in calves
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Additional file 6 of Microbiome diversity declines while distinct expansions of Th17, iNKT, and dendritic cell subpopulations emerge after anastomosis surgery
Vomhof‐DeKrey, E. E., Stover, A. D., & Basson, M. D. (2021) · Figshare · doi:10.6084/m9.figshare.15145808
Additional file 8 of Microbiome diversity declines while distinct expansions of Th17, iNKT, and dendritic cell subpopulations emerge after anastomosis surgery
Vomhof‐DeKrey, E. E., Stover, A. D., & Basson, M. D. (2021) · Figshare · doi:10.6084/m9.figshare.15145814
Additional file 10 of Microbiome diversity declines while distinct expansions of Th17, iNKT, and dendritic cell subpopulations emerge after anastomosis surgery
Vomhof‐DeKrey, E. E., Stover, A. D., & Basson, M. D. (2021) · Figshare · doi:10.6084/m9.figshare.15145790
Additional file 9 of Microbiome diversity declines while distinct expansions of Th17, iNKT, and dendritic cell subpopulations emerge after anastomosis surgery
Vomhof‐DeKrey, E. E., Stover, A. D., & Basson, M. D. (2021) · Figshare · doi:10.6084/m9.figshare.15145817
Additional file 1 of Host metabolome and faecal microbiome shows potential interactions impacted by age and weaning times in calves
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Additional file 1 of Microbiome diversity declines while distinct expansions of Th17, iNKT, and dendritic cell subpopulations emerge after anastomosis surgery
Vomhof‐DeKrey, E. E., Stover, A. D., & Basson, M. D. (2021) · Figshare · doi:10.6084/m9.figshare.15145793
Additional file 5 of Microbiome diversity declines while distinct expansions of Th17, iNKT, and dendritic cell subpopulations emerge after anastomosis surgery
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Authors: Alam, A., & Neish, A.
Affiliations: Emory University (US)
Corresponding author: Alam, Ashfaqul
ORCID: Alam, Ashfaqul
Neish, Andrew
Venue: Tissue Barriers
Publisher: Informa UK Limited
Published: 2018-07-03
Volume: 6
Issue: 3
Pages: 1539595
ISSN: 2168-8362 (ISSN-L)
2168-8370
DOI: 10.1080/21688370.2018.1539595
PMC: PMC6389125
OpenAlex: W2899740161
Cited by: 166
References: 152
Citations by year: 2026: 14 · 2025: 17 · 2024: 28 · 2023: 20 · 2022: 26 · 2021: 40 · 2020: 12 · 2019: 9
FWCI: 1.49
Type: journal article
Language: en
Open access: bronze
doi.org
Locations: Tissue Barriers (publishedVersion)
Europe PMC (PubMed Central) (publishedVersion)
PubMed Central (publishedVersion)
PubMed (publishedVersion)
Funders: National Cancer Institute (5R01CA179424)
National Institutes of Health (R01AI064462, K01DK114391)
Topics: Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
Health Sciences › Medicine › Gastroenterology › Gastrointestinal motility and disorders
Health Sciences › Medicine › Gastroenterology › Inflammatory Bowel Disease
Keywords: gut microbiota, intestinal barrier function, intestinal wound healing, mucosal regeneration, dysbiosis, intestinal diseases, mucosal injury, host-microbe interactions
MeSH terms: Gastrointestinal Microbiome, Intestinal Mucosa, Wound Healing

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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.

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Role of gut microbiota in intestinal wound healing and barrier function

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