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Small intestine vs. colon ecology and physiology: Why it matters in probiotic administration
Research on gut microbiota has generally focused on fecal samples, representing luminal content of the large intestine. However, nutrient uptake is restricted to the small intestine. Abundant immune cell populations at this anatomical site combined with diminished mucus secretion and looser junction...
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/PMC10518632/ https://www.ncbi.nlm.nih.gov/pubmed/37683651 http://dx.doi.org/10.1016/j.xcrm.2023.101190 |
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author | Jensen, Benjamin Anderschou Holbech Heyndrickx, Marc Jonkers, Daisy Mackie, Alan Millet, Sam Naghibi, Malwina Pærregaard, Simone Isling Pot, Bruno Saulnier, Delphine Sina, Christian Sterkman, Luc Gerardus Willibrordus Van den Abbeele, Pieter Venlet, Naomi Vita Zoetendal, Erwin G. Ouwehand, Arthur Constantijn |
author_facet | Jensen, Benjamin Anderschou Holbech Heyndrickx, Marc Jonkers, Daisy Mackie, Alan Millet, Sam Naghibi, Malwina Pærregaard, Simone Isling Pot, Bruno Saulnier, Delphine Sina, Christian Sterkman, Luc Gerardus Willibrordus Van den Abbeele, Pieter Venlet, Naomi Vita Zoetendal, Erwin G. Ouwehand, Arthur Constantijn |
author_sort | Jensen, Benjamin Anderschou Holbech |
collection | PubMed |
description | Research on gut microbiota has generally focused on fecal samples, representing luminal content of the large intestine. However, nutrient uptake is restricted to the small intestine. Abundant immune cell populations at this anatomical site combined with diminished mucus secretion and looser junctions (partly to allow for more efficient fluid and nutrient absorption) also results in intimate host-microbe interactions despite more rapid transit. It is thus crucial to dissect key differences in both ecology and physiology between small and large intestine to better leverage the immense potential of human gut microbiota imprinting, including probiotic engraftment at biological sensible niches. Here, we provide a detailed review unfolding how the physiological and anatomical differences between the small and large intestine affect gut microbiota composition, function, and plasticity. This information is key to understanding how gut microbiota manipulation, including probiotic administration, may strain-dependently transform host-microbe interactions at defined locations. |
format | Online Article Text |
id | pubmed-10518632 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-105186322023-09-26 Small intestine vs. colon ecology and physiology: Why it matters in probiotic administration Jensen, Benjamin Anderschou Holbech Heyndrickx, Marc Jonkers, Daisy Mackie, Alan Millet, Sam Naghibi, Malwina Pærregaard, Simone Isling Pot, Bruno Saulnier, Delphine Sina, Christian Sterkman, Luc Gerardus Willibrordus Van den Abbeele, Pieter Venlet, Naomi Vita Zoetendal, Erwin G. Ouwehand, Arthur Constantijn Cell Rep Med Review Research on gut microbiota has generally focused on fecal samples, representing luminal content of the large intestine. However, nutrient uptake is restricted to the small intestine. Abundant immune cell populations at this anatomical site combined with diminished mucus secretion and looser junctions (partly to allow for more efficient fluid and nutrient absorption) also results in intimate host-microbe interactions despite more rapid transit. It is thus crucial to dissect key differences in both ecology and physiology between small and large intestine to better leverage the immense potential of human gut microbiota imprinting, including probiotic engraftment at biological sensible niches. Here, we provide a detailed review unfolding how the physiological and anatomical differences between the small and large intestine affect gut microbiota composition, function, and plasticity. This information is key to understanding how gut microbiota manipulation, including probiotic administration, may strain-dependently transform host-microbe interactions at defined locations. Elsevier 2023-09-07 /pmc/articles/PMC10518632/ /pubmed/37683651 http://dx.doi.org/10.1016/j.xcrm.2023.101190 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 | Review Jensen, Benjamin Anderschou Holbech Heyndrickx, Marc Jonkers, Daisy Mackie, Alan Millet, Sam Naghibi, Malwina Pærregaard, Simone Isling Pot, Bruno Saulnier, Delphine Sina, Christian Sterkman, Luc Gerardus Willibrordus Van den Abbeele, Pieter Venlet, Naomi Vita Zoetendal, Erwin G. Ouwehand, Arthur Constantijn Small intestine vs. colon ecology and physiology: Why it matters in probiotic administration |
title | Small intestine vs. colon ecology and physiology: Why it matters in probiotic administration |
title_full | Small intestine vs. colon ecology and physiology: Why it matters in probiotic administration |
title_fullStr | Small intestine vs. colon ecology and physiology: Why it matters in probiotic administration |
title_full_unstemmed | Small intestine vs. colon ecology and physiology: Why it matters in probiotic administration |
title_short | Small intestine vs. colon ecology and physiology: Why it matters in probiotic administration |
title_sort | small intestine vs. colon ecology and physiology: why it matters in probiotic administration |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10518632/ https://www.ncbi.nlm.nih.gov/pubmed/37683651 http://dx.doi.org/10.1016/j.xcrm.2023.101190 |
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