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

Autor: Cristina Lupu, Robert Silasi, Girija Regmi, Ravi S. Keshari, Kathryn Burge, Misty Good, Florea Lupu, Majoi A. Trammell, Hala Chaaban, Steven J. McElroy, Jeffrey Eckert, David W. Dyer
Jazyk: angličtina
Rok vydání: 2021
Předmět:
0301 basic medicine
Small
Mice
0302 clinical medicine
Intestine
Small

2.1 Biological and endogenous factors
TX341-641
Intestinal Mucosa
Hyaluronic Acid
Pediatric
Nutrition and Dietetics
Cell Differentiation
Intestine
Intestines
medicine.anatomical_structure
Goblet Cells
Pediatric Research Initiative
Paneth Cells
1.1 Normal biological development and functioning
Crypt
Biology
digestive system
Article
Microbiology
hyaluronan
03 medical and health sciences
Food Sciences
Downregulation and upregulation
medicine
Animals
Microbiome
preterm infants
Nutrition
Cell Proliferation
Goblet cell
necrotizing enterocolitis
human milk bioactive factors
Nutrition. Foods and food supply
Cell growth
Lachnospiraceae
Perinatal Period - Conditions Originating in Perinatal Period
Newborn
Small intestine
Gastrointestinal Microbiome
intestinal barrier
030104 developmental biology
Animals
Newborn

Dietary Supplements
Colostrum
Digestive Diseases
prebiotics
030217 neurology & neurosurgery
Food Science
Zdroj: Nutrients
Nutrients, vol 13, iss 6
Nutrients, Vol 13, Iss 2030, p 2030 (2021)
Volume 13
Issue 6
ISSN: 2072-6643
Popis: 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.
Databáze: OpenAIRE