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Alterations of the intestinal mucus layer correlate with dysbiosis and immune dysregulation in human Type 1 Diabetes
BACKGROUND: In preclinical models of Type 1 Diabetes (T1D) the integrity of the gut barrier (GB) is instrumental to avoid dysregulated crosstalk between the commensal microbiota and immune cells and to prevent autoimmunity. The GB is composed of the intestinal epithelial barrier (IEB) and of the muc...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10139895/ https://www.ncbi.nlm.nih.gov/pubmed/37062177 http://dx.doi.org/10.1016/j.ebiom.2023.104567 |
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author | Lo Conte, Marta Cosorich, Ilaria Ferrarese, Roberto Antonini Cencicchio, Martina Nobili, Angelica Palmieri, Vittoria Massimino, Luca Lamparelli, Luigi Antonio Liang, Wenjie Riba, Michela Devecchi, Elisabetta Bolla, Andrea Mario Pedone, Erika Scavini, Marina Bosi, Emanuele Fasano, Alessio Ungaro, Federica Diana, Julien Mancini, Nicasio Falcone, Marika |
author_facet | Lo Conte, Marta Cosorich, Ilaria Ferrarese, Roberto Antonini Cencicchio, Martina Nobili, Angelica Palmieri, Vittoria Massimino, Luca Lamparelli, Luigi Antonio Liang, Wenjie Riba, Michela Devecchi, Elisabetta Bolla, Andrea Mario Pedone, Erika Scavini, Marina Bosi, Emanuele Fasano, Alessio Ungaro, Federica Diana, Julien Mancini, Nicasio Falcone, Marika |
author_sort | Lo Conte, Marta |
collection | PubMed |
description | BACKGROUND: In preclinical models of Type 1 Diabetes (T1D) the integrity of the gut barrier (GB) is instrumental to avoid dysregulated crosstalk between the commensal microbiota and immune cells and to prevent autoimmunity. The GB is composed of the intestinal epithelial barrier (IEB) and of the mucus layer containing mucins and antimicrobial peptides (AMPs) that are crucial to maintain immune tolerance. In preclinical models of T1D the alterations of the GB primarily affect the mucus layer. In human T1D increased gut permeability and IEB damage have been demonstrated but the integrity of the mucus layer was never assessed. METHODS: We evaluated GB integrity by measuring serological markers of IEB damage (serological levels of zonulin) and bacterial translocation such as lipopolysaccharide binding protein (LBP) and myeloid differentiation protein 2 (MD2), and mRNA expression of tight junction proteins, mucins and AMPs in intestinal tissue of T1D patients and healthy controls (HC). Simultaneously, we performed immunological profiling on intestinal tissue and 16S rRNA analysis on the mucus-associated gut microbiota (MAGM). FINDINGS: Our data show a GB damage with mucus layer alterations and reduced mRNA expression of several mucins (MUC2, MUC12, MUC13, MUC15, MUC20, MUC21) and AMPs (HD4 and HD5) in T1D patients. Mucus layer alterations correlated with reduced relative abundance of short chain fatty acids (SCFA)-producing bacteria such as Bifidobacterium dentium, Clostridium butyricum and Roseburia intestinalis that regulate mucin expression and intestinal immune homeostasis. In T1D patients we also found intestinal immune dysregulation with higher percentages of effector T cells such as T helper (Th) 1, Th17 and TNF-α(+) T cells. INTERPRETATION: Our data show that mucus layer alterations are present in T1D subjects and associated with dysbiosis and immune dysregulation. FUNDING: Research Grants from the Juvenile Diabetes Foundation (Grant 1-INO-2018-640-A-N to MF and 2-SRA-2019-680-S-B to JD) and from the 10.13039/501100003196Italian Ministry of Health (Grant RF19-12370721 to MF). |
format | Online Article Text |
id | pubmed-10139895 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-101398952023-04-29 Alterations of the intestinal mucus layer correlate with dysbiosis and immune dysregulation in human Type 1 Diabetes Lo Conte, Marta Cosorich, Ilaria Ferrarese, Roberto Antonini Cencicchio, Martina Nobili, Angelica Palmieri, Vittoria Massimino, Luca Lamparelli, Luigi Antonio Liang, Wenjie Riba, Michela Devecchi, Elisabetta Bolla, Andrea Mario Pedone, Erika Scavini, Marina Bosi, Emanuele Fasano, Alessio Ungaro, Federica Diana, Julien Mancini, Nicasio Falcone, Marika eBioMedicine Articles BACKGROUND: In preclinical models of Type 1 Diabetes (T1D) the integrity of the gut barrier (GB) is instrumental to avoid dysregulated crosstalk between the commensal microbiota and immune cells and to prevent autoimmunity. The GB is composed of the intestinal epithelial barrier (IEB) and of the mucus layer containing mucins and antimicrobial peptides (AMPs) that are crucial to maintain immune tolerance. In preclinical models of T1D the alterations of the GB primarily affect the mucus layer. In human T1D increased gut permeability and IEB damage have been demonstrated but the integrity of the mucus layer was never assessed. METHODS: We evaluated GB integrity by measuring serological markers of IEB damage (serological levels of zonulin) and bacterial translocation such as lipopolysaccharide binding protein (LBP) and myeloid differentiation protein 2 (MD2), and mRNA expression of tight junction proteins, mucins and AMPs in intestinal tissue of T1D patients and healthy controls (HC). Simultaneously, we performed immunological profiling on intestinal tissue and 16S rRNA analysis on the mucus-associated gut microbiota (MAGM). FINDINGS: Our data show a GB damage with mucus layer alterations and reduced mRNA expression of several mucins (MUC2, MUC12, MUC13, MUC15, MUC20, MUC21) and AMPs (HD4 and HD5) in T1D patients. Mucus layer alterations correlated with reduced relative abundance of short chain fatty acids (SCFA)-producing bacteria such as Bifidobacterium dentium, Clostridium butyricum and Roseburia intestinalis that regulate mucin expression and intestinal immune homeostasis. In T1D patients we also found intestinal immune dysregulation with higher percentages of effector T cells such as T helper (Th) 1, Th17 and TNF-α(+) T cells. INTERPRETATION: Our data show that mucus layer alterations are present in T1D subjects and associated with dysbiosis and immune dysregulation. FUNDING: Research Grants from the Juvenile Diabetes Foundation (Grant 1-INO-2018-640-A-N to MF and 2-SRA-2019-680-S-B to JD) and from the 10.13039/501100003196Italian Ministry of Health (Grant RF19-12370721 to MF). Elsevier 2023-04-14 /pmc/articles/PMC10139895/ /pubmed/37062177 http://dx.doi.org/10.1016/j.ebiom.2023.104567 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Articles Lo Conte, Marta Cosorich, Ilaria Ferrarese, Roberto Antonini Cencicchio, Martina Nobili, Angelica Palmieri, Vittoria Massimino, Luca Lamparelli, Luigi Antonio Liang, Wenjie Riba, Michela Devecchi, Elisabetta Bolla, Andrea Mario Pedone, Erika Scavini, Marina Bosi, Emanuele Fasano, Alessio Ungaro, Federica Diana, Julien Mancini, Nicasio Falcone, Marika Alterations of the intestinal mucus layer correlate with dysbiosis and immune dysregulation in human Type 1 Diabetes |
title | Alterations of the intestinal mucus layer correlate with dysbiosis and immune dysregulation in human Type 1 Diabetes |
title_full | Alterations of the intestinal mucus layer correlate with dysbiosis and immune dysregulation in human Type 1 Diabetes |
title_fullStr | Alterations of the intestinal mucus layer correlate with dysbiosis and immune dysregulation in human Type 1 Diabetes |
title_full_unstemmed | Alterations of the intestinal mucus layer correlate with dysbiosis and immune dysregulation in human Type 1 Diabetes |
title_short | Alterations of the intestinal mucus layer correlate with dysbiosis and immune dysregulation in human Type 1 Diabetes |
title_sort | alterations of the intestinal mucus layer correlate with dysbiosis and immune dysregulation in human type 1 diabetes |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10139895/ https://www.ncbi.nlm.nih.gov/pubmed/37062177 http://dx.doi.org/10.1016/j.ebiom.2023.104567 |
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