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Acceleration of Small Intestine Development and Remodeling of the Microbiome Following Hyaluronan 35 kDa Treatment in Neonatal Mice

The beneficial effects of human milk suppressing the development of intestinal pathologies such as necrotizing enterocolitis in preterm infants are widely known. Human milk (HM) is rich in a multitude of bioactive factors that play major roles in promoting postnatal maturation, differentiation, and...

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Autores principales: Chaaban, Hala, Burge, Kathryn, Eckert, Jeffrey, Trammell, MaJoi, Dyer, David, Keshari, Ravi S., Silasi, Robert, Regmi, Girija, Lupu, Cristina, Good, Misty, McElroy, Steven J., Lupu, Florea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8231646/
https://www.ncbi.nlm.nih.gov/pubmed/34204790
http://dx.doi.org/10.3390/nu13062030
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author Chaaban, Hala
Burge, Kathryn
Eckert, Jeffrey
Trammell, MaJoi
Dyer, David
Keshari, Ravi S.
Silasi, Robert
Regmi, Girija
Lupu, Cristina
Good, Misty
McElroy, Steven J.
Lupu, Florea
author_facet Chaaban, Hala
Burge, Kathryn
Eckert, Jeffrey
Trammell, MaJoi
Dyer, David
Keshari, Ravi S.
Silasi, Robert
Regmi, Girija
Lupu, Cristina
Good, Misty
McElroy, Steven J.
Lupu, Florea
author_sort Chaaban, Hala
collection PubMed
description The beneficial effects of human milk suppressing the development of intestinal pathologies such as necrotizing enterocolitis in preterm infants are widely known. Human milk (HM) is rich in a multitude of bioactive factors that play major roles in promoting postnatal maturation, differentiation, and the development of the microbiome. Previous studies showed that HM is rich in hyaluronan (HA) especially in colostrum and early milk. This study aims to determine the role of HA 35 KDa, a HM HA mimic, on intestinal proliferation, differentiation, and the development of the intestinal microbiome. We show that oral HA 35 KDa supplementation for 7 days in mouse pups leads to increased villus length and crypt depth, and increased goblet and Paneth cells, compared to controls. We also show that HA 35 KDa leads to an increased predominance of Clostridiales Ruminococcaceae, Lactobacillales Lactobacillaceae, and Clostridiales Lachnospiraceae. In seeking the mechanisms involved in the changes, bulk RNA seq was performed on samples from the terminal ileum and identified upregulation in several genes essential for cellular growth, proliferation, and survival. Taken together, this study shows that HA 35 KDa supplemented to mouse pups promotes intestinal epithelial cell proliferation, as well as the development of Paneth cells and goblet cell subsets. HA 35 KDa also impacted the intestinal microbiota; the implications of these responses need to be determined.
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spelling pubmed-82316462021-06-26 Acceleration of Small Intestine Development and Remodeling of the Microbiome Following Hyaluronan 35 kDa Treatment in Neonatal Mice Chaaban, Hala Burge, Kathryn Eckert, Jeffrey Trammell, MaJoi Dyer, David Keshari, Ravi S. Silasi, Robert Regmi, Girija Lupu, Cristina Good, Misty McElroy, Steven J. Lupu, Florea Nutrients Article The beneficial effects of human milk suppressing the development of intestinal pathologies such as necrotizing enterocolitis in preterm infants are widely known. Human milk (HM) is rich in a multitude of bioactive factors that play major roles in promoting postnatal maturation, differentiation, and the development of the microbiome. Previous studies showed that HM is rich in hyaluronan (HA) especially in colostrum and early milk. This study aims to determine the role of HA 35 KDa, a HM HA mimic, on intestinal proliferation, differentiation, and the development of the intestinal microbiome. We show that oral HA 35 KDa supplementation for 7 days in mouse pups leads to increased villus length and crypt depth, and increased goblet and Paneth cells, compared to controls. We also show that HA 35 KDa leads to an increased predominance of Clostridiales Ruminococcaceae, Lactobacillales Lactobacillaceae, and Clostridiales Lachnospiraceae. In seeking the mechanisms involved in the changes, bulk RNA seq was performed on samples from the terminal ileum and identified upregulation in several genes essential for cellular growth, proliferation, and survival. Taken together, this study shows that HA 35 KDa supplemented to mouse pups promotes intestinal epithelial cell proliferation, as well as the development of Paneth cells and goblet cell subsets. HA 35 KDa also impacted the intestinal microbiota; the implications of these responses need to be determined. MDPI 2021-06-12 /pmc/articles/PMC8231646/ /pubmed/34204790 http://dx.doi.org/10.3390/nu13062030 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Chaaban, Hala
Burge, Kathryn
Eckert, Jeffrey
Trammell, MaJoi
Dyer, David
Keshari, Ravi S.
Silasi, Robert
Regmi, Girija
Lupu, Cristina
Good, Misty
McElroy, Steven J.
Lupu, Florea
Acceleration of Small Intestine Development and Remodeling of the Microbiome Following Hyaluronan 35 kDa Treatment in Neonatal Mice
title Acceleration of Small Intestine Development and Remodeling of the Microbiome Following Hyaluronan 35 kDa Treatment in Neonatal Mice
title_full Acceleration of Small Intestine Development and Remodeling of the Microbiome Following Hyaluronan 35 kDa Treatment in Neonatal Mice
title_fullStr Acceleration of Small Intestine Development and Remodeling of the Microbiome Following Hyaluronan 35 kDa Treatment in Neonatal Mice
title_full_unstemmed Acceleration of Small Intestine Development and Remodeling of the Microbiome Following Hyaluronan 35 kDa Treatment in Neonatal Mice
title_short Acceleration of Small Intestine Development and Remodeling of the Microbiome Following Hyaluronan 35 kDa Treatment in Neonatal Mice
title_sort acceleration of small intestine development and remodeling of the microbiome following hyaluronan 35 kda treatment in neonatal mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8231646/
https://www.ncbi.nlm.nih.gov/pubmed/34204790
http://dx.doi.org/10.3390/nu13062030
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