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Breast milk nutrients driving intestinal epithelial layer maturation via Wnt and Notch signaling: Implications for necrotizing enterocolitis
- Source :
- Biochimica et biophysica acta. Molecular basis of disease. 1867(11)
- Publication Year :
- 2021
-
Abstract
- Necrotizing enterocolitis (NEC) is an often lethal, inflammatory disease of the preterm intestine. The underdeveloped immune system plays an important role; however, the initial trigger for NEC development is likely a damaged intestinal epithelial layer. We hypothesize that due to incomplete maturation of different epithelial cell lineages, nutrients and bacteria are able to damage the epithelial cells and cause the (immature) inflammatory response, food intolerance and malabsorption seen in NEC. Intestinal organoid research has shown that maturation of intestinal epithelial cell lineages is orchestrated by two key signaling pathways: Wnt and Notch. In NEC, these pathways are dysregulated by hyperactivation of Toll-like-receptor-4. Breastfeeding decreases the risk of developing NEC compared to formula milk. Here, we review the intricate link between breast milk components, Wnt and Notch signaling and intestinal epithelial maturation. We argue that (nutritional) interventions regulating these pathways may decrease the risk of NEC development in preterm infants.
- Subjects :
- Malabsorption
Notch signaling pathway
Biology
Breast milk
Immune system
Enterocolitis, Necrotizing
medicine
Humans
Intestinal Mucosa
Molecular Biology
Wnt Signaling Pathway
Milk, Human
Receptors, Notch
Wnt signaling pathway
Infant, Newborn
Nutrients
medicine.disease
digestive system diseases
Epithelium
Toll-Like Receptor 4
Wnt Proteins
medicine.anatomical_structure
Breast Feeding
Necrotizing enterocolitis
Cancer research
Molecular Medicine
Signal transduction
Infant, Premature
Signal Transduction
Subjects
Details
- ISSN :
- 1879260X
- Volume :
- 1867
- Issue :
- 11
- Database :
- OpenAIRE
- Journal :
- Biochimica et biophysica acta. Molecular basis of disease
- Accession number :
- edsair.doi.dedup.....51fe1d7240535c3ad523b38c610cb38a