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Human Milk Oligosaccharides Protect against Necrotizing Enterocolitis by Activating Intestinal Cell Differentiation.

Authors :
Li B
Wu RY
Horne RG
Ahmed A
Lee D
Robinson SC
Zhu H
Lee C
Cadete M
Johnson-Henry KC
Landberg E
Alganabi M
Abrahamsson T
Delgado-Olguin P
Pierro A
Sherman PM
Source :
Molecular nutrition & food research [Mol Nutr Food Res] 2020 Nov; Vol. 64 (21), pp. e2000519. Date of Electronic Publication: 2020 Oct 04.
Publication Year :
2020

Abstract

Scope: Necrotizing enterocolitis (NEC) is a devastating gastrointestinal emergency and currently the leading cause of mortality in preterm infants. Recent studies show that human milk oligosaccharides (HMOs) reduce the frequency and incidence of NEC; however, the molecular mechanisms for their protection are largely unexplored.<br />Methods and Results: To address this gap, a genome-wide profiling of the intestinal epithelial transcriptome in response to HMOs using RNA-sequencing is performed. It is found that HMOs alter the host transcriptome in 225 unique target genes pertaining to cell proliferation and differentiation, including upregulation of stem cell differentiation marker HMGCS2. To validate these results, differentiation in Caco-2Bbe1 (Caco-2) intestinal cells is verified by Alcian Blue staining and transepithelial electrical resistance (TER) recordings. Furthermore, an in vivo model of NEC is also employed whereby neonatal pups are gavage fed HMOs. Interestingly, HMOs-fed pups show enhanced cell MUC2 differentiation and HMGCS2 expression.<br />Conclusions: These findings demonstrate HMOs protect against NEC in part by altering the differentiation of the crypt-villus axis. In addition, this study suggests that pooled HMOs directly induce a series of biological processes, which provide mechanistic insights to how HMOs protect the host intestine.<br /> (© 2020 Wiley-VCH GmbH.)

Details

Language :
English
ISSN :
1613-4133
Volume :
64
Issue :
21
Database :
MEDLINE
Journal :
Molecular nutrition & food research
Publication Type :
Academic Journal
Accession number :
32926533
Full Text :
https://doi.org/10.1002/mnfr.202000519