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The impact of indole-3-lactic acid on immature intestinal innate immunity and development: a transcriptomic analysis
An excessive intestinal inflammatory response may have a role in the pathogenesis of necrotizing enterocolitis (NEC) in very preterm infants. Indole-3-lactic acid (ILA) of breastmilk tryptophan was identified as the anti-inflammatory metabolite involved in probiotic conditioned media from Bifidobact...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8044159/ https://www.ncbi.nlm.nih.gov/pubmed/33850185 http://dx.doi.org/10.1038/s41598-021-87353-1 |
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author | Huang, Wuyang Cho, Ky Young Meng, Di Walker, W. Allan |
author_facet | Huang, Wuyang Cho, Ky Young Meng, Di Walker, W. Allan |
author_sort | Huang, Wuyang |
collection | PubMed |
description | An excessive intestinal inflammatory response may have a role in the pathogenesis of necrotizing enterocolitis (NEC) in very preterm infants. Indole-3-lactic acid (ILA) of breastmilk tryptophan was identified as the anti-inflammatory metabolite involved in probiotic conditioned media from Bifidobacteria longum subsp infantis. This study aimed to explore the molecular endocytic pathways involved in the protective ILA effect against inflammation. H4 cells, Caco-2 cells, C57BL/6 pup and adult mice were used to compare the anti-inflammatory mechanisms between immature and mature enterocytes in vitro and in vivo. The results show that ILA has pleiotropic protective effects on immature enterocytes including anti-inflammatory, anti-viral, and developmental regulatory potentials in a region-dependent and an age-dependent manner. Quantitative transcriptomic analysis revealed a new mechanistic model in which STAT1 pathways play an important role in IL-1β-induced inflammation and ILA has a regulatory effect on STAT1 pathways. These studies were validated by real-time RT-qPCR and STAT1 inhibitor experiments. Different protective reactions of ILA between immature and mature enterocytes indicated that ILA’s effects are developmentally regulated. These findings may be helpful in preventing NEC for premature infants. |
format | Online Article Text |
id | pubmed-8044159 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-80441592021-04-14 The impact of indole-3-lactic acid on immature intestinal innate immunity and development: a transcriptomic analysis Huang, Wuyang Cho, Ky Young Meng, Di Walker, W. Allan Sci Rep Article An excessive intestinal inflammatory response may have a role in the pathogenesis of necrotizing enterocolitis (NEC) in very preterm infants. Indole-3-lactic acid (ILA) of breastmilk tryptophan was identified as the anti-inflammatory metabolite involved in probiotic conditioned media from Bifidobacteria longum subsp infantis. This study aimed to explore the molecular endocytic pathways involved in the protective ILA effect against inflammation. H4 cells, Caco-2 cells, C57BL/6 pup and adult mice were used to compare the anti-inflammatory mechanisms between immature and mature enterocytes in vitro and in vivo. The results show that ILA has pleiotropic protective effects on immature enterocytes including anti-inflammatory, anti-viral, and developmental regulatory potentials in a region-dependent and an age-dependent manner. Quantitative transcriptomic analysis revealed a new mechanistic model in which STAT1 pathways play an important role in IL-1β-induced inflammation and ILA has a regulatory effect on STAT1 pathways. These studies were validated by real-time RT-qPCR and STAT1 inhibitor experiments. Different protective reactions of ILA between immature and mature enterocytes indicated that ILA’s effects are developmentally regulated. These findings may be helpful in preventing NEC for premature infants. Nature Publishing Group UK 2021-04-13 /pmc/articles/PMC8044159/ /pubmed/33850185 http://dx.doi.org/10.1038/s41598-021-87353-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Huang, Wuyang Cho, Ky Young Meng, Di Walker, W. Allan The impact of indole-3-lactic acid on immature intestinal innate immunity and development: a transcriptomic analysis |
title | The impact of indole-3-lactic acid on immature intestinal innate immunity and development: a transcriptomic analysis |
title_full | The impact of indole-3-lactic acid on immature intestinal innate immunity and development: a transcriptomic analysis |
title_fullStr | The impact of indole-3-lactic acid on immature intestinal innate immunity and development: a transcriptomic analysis |
title_full_unstemmed | The impact of indole-3-lactic acid on immature intestinal innate immunity and development: a transcriptomic analysis |
title_short | The impact of indole-3-lactic acid on immature intestinal innate immunity and development: a transcriptomic analysis |
title_sort | impact of indole-3-lactic acid on immature intestinal innate immunity and development: a transcriptomic analysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8044159/ https://www.ncbi.nlm.nih.gov/pubmed/33850185 http://dx.doi.org/10.1038/s41598-021-87353-1 |
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