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Age-Associated Remodeling of the Intestinal Epithelial Barrier
Open accessAbstract
Disorders of the gastrointestinal tract are common in the elderly people; however, the precise trait(s) of aging that contribute to the vulnerability of the gastrointestinal tract are poorly understood. Recent evidence suggests that patients with gastrointestinal disorders have increased intestinal permeability. Here, we address the hypothesis that disruption of the intestinal barrier is associated with aging. Our results demonstrated that permeability was significantly higher in colonic biopsies collected from old baboons compared with young baboons. Additionally, colonic tissue from the older animals had decreased zonula occluden-1, occludin, and junctional adhesion molecule-A tight junction protein expression and increased claudin-2 expression. Upregulation of miR-29a and inflammatory cytokines IFN-γ, IL-6, and IL-1β was also found in colonic biopsies from old baboons relative to young baboons. These results show for the first time that a pivotal contributing factor to geriatric vulnerability to gastrointestinal dysfunction may be increased colonic permeability via age-associated remodeling of intestinal epithelial tight junction proteins.
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“In the aged GI tract, compromised epithelial and mucosal cell turnover, integrity, and function [32, 36, 76, 83] can lead to increased epithelial barrier permeability [19, 75, 118, 120]”
From Fecal microbiota transfer between young and aged mice reverses hallmarks of the aging gut, eye, and brain (2022) · cites this paper as [120]
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Cites
Interactions Between the Microbiota and the Immune System
Hooper, L. V., Littman, D. R., & Macpherson, A. J. (2012) · Science · doi:10.1126/science.1223490 · Cited by 4,173
Intestinal mucosal barrier function in health and disease
Turner, J. R. (2009) · Nature reviews. Immunology · doi:10.1038/nri2653 · Cited by 3,952
Through Ageing, and Beyond: Gut Microbiota and Inflammatory Status in Seniors and Centenarians
Biagi, E., Nylund, L., Candela, M., Ostan, R., Bucci, L., Pini, E., Nikkïla, J., Monti, D., Satokari, R., Franceschi, C., et al. (2010) · PLoS ONE · doi:10.1371/journal.pone.0010667 · Cited by 1,483
Zeißig, S., Bürgel, N., Günzel, D., Richter, J. F., Mankertz, J., Wahnschaffe, U., Kroesen, A. J., Zeitz, M., Fromm, M., & Schulzke, J. (2006) · Gut · doi:10.1136/gut.2006.094375 · Cited by 1,218
Intestinal barrier function in health and gastrointestinal disease
Camilleri, M., Madsen, K., Spiller, R., Van Meerveld, B. G., & Verne, G. N. (2012) · Neurogastroenterology & Motility · doi:10.1111/j.1365-2982.2012.01921.x · Cited by 908
Interferon-gamma directly affects barrier function of cultured intestinal epithelial monolayers.
Madara, J. L., & Stafford, J. (1989) · Journal of Clinical Investigation · doi:10.1172/jci113938 · Cited by 758
Cytokine regulation of tight junctions
Capaldo, C., & Nusrat, A. (2008) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2008.08.027 · Cited by 747
Electrolyte transport in the mammalian colon: mechanisms and implications for disease
Kunzelmann, K., & Mall, M. (2002) · Physiological Reviews · doi:10.1152/physrev.00026.2001 · Cited by 655
Mechanism of cytokine modulation of epithelial tight junction barrier
Al–Sadi, R. (2009) · Frontiers in bioscience · doi:10.2741/3413 · Cited by 649
IL-1β Causes an Increase in Intestinal Epithelial Tight Junction Permeability
Al-Sadi, R. M., & Ma, T. Y. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.178.7.4641 · Cited by 601
Research works printed but not linked: 3
- Zhu, 2000, Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae, 22, 425
- Ershler, 1993, Lymphokine and cytokine research, 12, 225
- 1995, American Journal of Physiology - Gastrointestinal and Liver Physiology, 268, R208
Cited by
Sorted by citations
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Wei, G., Liu, W., Shen, F., Xie, R., Wang, F., Guo, H., & Liu, L. (2025) · Journal of Environmental Sciences · doi:10.1016/j.jes.2025.05.036 · Cited by 7
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Brai, E., & Alberi, L. A. (2018) · InTech eBooks · doi:10.5772/intechopen.75061 · Cited by 9
Paillaud, É., Bastuji‐Garin, S., Plonquet, A., Foucat, E., Fournier, B., Boutin, E., Thuaut, A. L., Lévy, Y., & Hüe, S. (2017) · The Journals of Gerontology Series A · doi:10.1093/gerona/glx106 · Cited by 8
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Miró, L., Moretó, M., Amat, C., Polo, J., & Pérez‐Bosque, A. (2020) · International Electronic Conference on Nutrients (IECN) · doi:10.3390/iecn2020-06995 · Cited by 7
Rodriguez‐Palacios, A., & Cominelli, F. (2018) · Inflammatory Bowel Diseases · doi:10.1093/ibd/izy197 · Cited by 7
Thirugnanam, S., & Rout, N. (2024) · Current Issues in Molecular Biology · doi:10.3390/cimb46050287 · Cited by 6
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Kuroda, A., Jaisue, J., Isobe, N., & Nii, T. (2025) · Poultry Science · doi:10.1016/j.psj.2025.106241 · Cited by 6
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Hodge, R. A., Ghannam, M., Edmond, E., de la Torre, F., D’Alterio, C., Kaya, N. H., Resnik-Docampo, M., Reiff, T., & Jones, D. L. (2023) · iScience · doi:10.1016/j.isci.2023.106901 · Cited by 6
Giri, S., Takada, A., Paudel, D., Uehara, O., Kurashige, Y., Kuramitsu, Y., Furukawa, M., Matsushita, K., Arakawa, T., Nagasawa, T., et al. (2024) · Journal of Oral Biosciences · doi:10.1016/j.job.2024.01.012 · Cited by 6
Søfteland, J. M., Casselbrant, A., Akyürek, L. M., Hellström, M., & Oltean, M. (2019) · Transplantation · doi:10.1097/tp.0000000000002999 · Cited by 6
Hattay, P., Prusator, D. K., Johnson, A. C., & Meerveld, B. G. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00543 · Cited by 6
Di, W., Lv, Y., Xia, F., Sheng, Y., Liu, J., & Ding, G. (2020) · Nutrition Research · doi:10.1016/j.nutres.2020.06.015 · Cited by 6
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Cansell, C., Goepp, V., Bain, F., Todd, N., Douard, V., Monnoye, M., Zane, F., Sanchez, C., Pietrancosta, N., Rovère, C., et al. (2025) · BMC Biology · doi:10.1186/s12915-025-02421-6 · Cited by 7
Kundaktepe, B. P., Karimova, A., & Onaran, İ. (2024) · Biogerontology · doi:10.1007/s10522-024-10102-0 · Cited by 5
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Wang, X., Liu, H., Yue, M., Wang, J., Zhang, C., Qin, L., Wang, S., & Hu, L. (2024) · Biogerontology · doi:10.1007/s10522-024-10127-5 · Cited by 5
Graeber, S. Y., Sommerburg, O., Yu, Y., Berges, J., Hirtz, S., Scheuermann, H., Berger, J., Duerr, J., & Mall, M. A. (2025) · Frontiers in Pharmacology · doi:10.3389/fphar.2025.1537095 · Cited by 4
Chen, N., Yu, Z., Ji, X., Zhang, S., Yu, C., Valencak, T. G., Shi, F., & Ren, D. (2025) · Current Research in Microbial Sciences · doi:10.1016/j.crmicr.2025.100381 · Cited by 4
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Ouerdane, Y., El-Nahas, Z. S., Ouerdane, F., Hamam, K. M., & Ebada, M. A. (2022) · Springer eBooks · doi:10.1007/978-981-16-7606-2_12 · Cited by 4
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Yang, L., Jiang, Z., Sun, Q., Karako, K., Yuan, L., & Song, P. (2025) · BioScience Trends · doi:10.5582/bst.2025.01279 · Cited by 2
D’Antongiovanni, V., Salvo, C. D., Valdiserra, G., Fornai, M., Cappelli, F., Mengozzi, A., Virdis, A., Masi, S., Duranti, E., Benvenuti, L., et al. (2026) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.70399 · Cited by 2
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Wu, Y., Cao, Q., & Liu, Q. (2026) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.67.4.16 · Cited by 2
Chandler, S. P., Palamuthusingam, D., Hawley, C. M., Pascoe, E. M., Johnson, D. W., & Fahim, M. (2026) · Peritoneal Dialysis International · doi:10.1177/08968608261444886 · Cited by 2
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胡, 旭., 金, 锋., & 王, 涛. (2016) · Scientia Sinica Vitae · doi:10.1360/n052016-0080 · Cited by 1
Conway, J., Rees, N. P., & Duggal, N. A. (2023) · Healthy ageing and longevity · doi:10.1007/978-3-031-14023-5_3 · Cited by 2
Robins, D., Lehmann, A., Krollik, K., & Vertzoni, M. (2024) · European Journal of Pharmaceutical Sciences · doi:10.1016/j.ejps.2024.106881 · Cited by 1
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Verboven, R., Verstraelen, P., Loose, N. D., Ott, J., Hanning, N., Winter, B. Y. D., Timmermans, J.-P., & Vos, W. H. D. (2026) · Biogerontology · doi:10.1007/s10522-026-10385-5 · Cited by 1
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Mi, X., Zhang, Y.-C., Xu-jun, Z., He, H., Chen, X.-C., & Dai, X. (2026) · Biology of Sex Differences · doi:10.1186/s13293-026-00905-w · Cited by 1
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Mornement, A. A., Dack, R. E., Doupé, D. P., & Clark, R. I. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.10.26.564159 · Cited by 1
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Vanhaecke, T. (2016) · theses.fr (ABES) · doi:10.70675/314bdbdfz4219z4db8zacd3z796751145682 · Cited by 1
Falutz, J. (2016) · Springer eBooks · doi:10.1007/978-3-319-20131-3_2
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Hanifeh, M. (2018) · Työväentutkimus Vuosikirja
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Keebaugh, E. S., Williams, L. D., & Ja, W. W. (2019) · Springer eBooks · doi:10.1007/978-3-030-28737-5_12
Rodis, B., & Tan, K. (2020) · Asian Journal of Gerontology and Geriatrics · doi:10.12809/ajgg-2018-324-cr
Kundaktepe, B. P., Karimova, A., & Onaran, İ. (2021) · Research Square · doi:10.21203/rs.3.rs-797246/v1
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GÓRSKA, A., Łętowska-Andrzejewicz, K., Andrzejewicz, P., Dobrowolski, P., Radzikowska-Büchner, E., Kuszta, P., & Łuszczewska‐Sierakowska, I. (2022) · Medycyna Weterynaryjna · doi:10.21521/mw.6705
Bashir, S., Wilson, M., Ashiru-Oredope, D. A. I., & Murdan, S. (2023) · AAPS advances in the pharmaceutical sciences series · doi:10.1007/978-3-031-35811-1_9
Jo, M. K., Moon, C. M., Jeon, H.-J., Han, Y., Lee, E. S., Kwon, J.-H., Yang, K., Ahn, Y., Kim, S., Jung, S.-A., et al. (2023) · Figshare · doi:10.6084/m9.figshare.23672631
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Churakov, G. A., BELYAKOV, M., Sall, T. S., & Орлов, С. В. (2025) · Molecular Biology · doi:10.1134/s0026893325700293
Patterson, K., Bermingham, E. N., Fraser, K., Bernstein, D. R., Weidgraaf, K., Shoveller, A. K. K., & Thomas, D. G. (2025) · Journal of Animal Physiology and Animal Nutrition · doi:10.1111/jpn.70015 · Cited by 1
Brossaud, R., Moullé, V. S. F., Giblaine, M., Even, S., Maillard, M.-B., Chevalier, S., Oullier, T., Guédon, É., Loir, Y. L., Cissé, M., et al. (2025) · Journal of Functional Foods · doi:10.1016/j.jff.2025.107095 · Cited by 1
Additional file 2 of The pleiotropic effects of prebiotic galacto-oligosaccharides on the aging gut
Arnold, J. W., Roach, J., Fabela, S., Moorfield, E., Ding, S., Blue, E., Dagher, S. F., Magness, S. T., Tamayo, R., Bruno-Bárcena, J. M., et al. (2021) · Figshare · doi:10.6084/m9.figshare.13662759
Additional file 5 of The pleiotropic effects of prebiotic galacto-oligosaccharides on the aging gut
Arnold, J. W., Roach, J., Fabela, S., Moorfield, E., Ding, S., Blue, E., Dagher, S. F., Magness, S. T., Tamayo, R., Bruno-Bárcena, J. M., et al. (2021) · Figshare · doi:10.6084/m9.figshare.13662774
Parker, A., Romano, S., Ansorge, R., Aboelnour, A., Le Gall, G., Savva, G. M., Pontifex, M. G., Telatin, A., Baker, D., Jones, E. J., et al. (2022) · Figshare · doi:10.6084/m9.figshare.19695986
Parker, A., Romano, S., Ansorge, R., Aboelnour, A., Le Gall, G., Savva, G. M., Pontifex, M. G., Telatin, A., Baker, D., Jones, E. J., et al. (2022) · Figshare · doi:10.6084/m9.figshare.19695980
Parker, A., Romano, S., Ansorge, R., Aboelnour, A., Le Gall, G., Savva, G. M., Pontifex, M. G., Telatin, A., Baker, D., Jones, E. J., et al. (2022) · Figshare · doi:10.6084/m9.figshare.19695974
Parker, A., Romano, S., Ansorge, R., Aboelnour, A., Le Gall, G., Savva, G. M., Pontifex, M. G., Telatin, A., Baker, D., Jones, E. J., et al. (2022) · Figshare · doi:10.6084/m9.figshare.19695983
Metadata
- Authors
- Tran, L., & Greenwood-Van Meerveld, B.
- Affiliations
- University of Oklahoma Health Sciences Center (US)
- ORCID
- Tran, L.
- Venue
- The Journals of Gerontology Series A: Biological Sciences and Medical Sciences
- Publisher
- Oxford University Press (OUP)
- Published
- 2013-07-20
- Volume
- 68
- Issue
- 9
- Pages
- 1045-1056
- ISSN
- 1079-5006 (ISSN-L)
- 1758-535X
- PMC
- PMC3738030
- OpenAlex
- W2161754779
- Cited by
- 320
- References
- 60
- Citations by year
- 2026: 25 · 2025: 28 · 2024: 25 · 2023: 27 · 2022: 37 · 2021: 31 · 2020: 25 · 2019: 29 · 2018: 22 · 2017: 32 · 2016: 18 · 2015: 9 · 2014: 10 · 2013: 2
- FWCI
- 12.28
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- The Journals of Gerontology Series A (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (P40OD010988)
- National Center for Research Resources (P40RR012317)
- Topics
- Health Sciences › Medicine › Gastroenterology › Gastrointestinal motility and disorders
- Life Sciences › Neuroscience › Neurology › Barrier Structure and Function Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Keywords
- intestinal permeability, intestinal barrier, aging, colonic epithelium, tight junction proteins, zonula occludens-1, occludin, claudin-2, JAM-A, miR-29a, inflammatory cytokines, interferon-gamma, interleukin-6, IL-1β, baboons
- MeSH terms
- Aging, Animals, Colon, Gastrointestinal Diseases, Glutamate-Ammonia Ligase, Humans, Intestinal Mucosa, Peroxidase, Permeability, Risk Factors, Cytokines, MicroRNAs, Papio anubis, Tight Junction Proteins
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