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Updated: Jan 4, 2026

Breast Milk Enhances Growth of Enteroids: An Ex Vivo Model of Cell Proliferation
Published on: February 15, 2018
Human breast milk exosomes attenuate intestinal damage
Hiromu Miyake1,2,3, Carol Lee1,2, Sinobol Chusilp1,2,4
1Division of General and Thoracic Surgery, The Hospital for Sick Children, University of Toronto, 1526-555 University Avenue, Toronto, ON, M5G 1X8, Canada.
Insights
Both raw and pasteurized human breast milk (HBM) exosomes effectively reduce intestinal inflammation and injury in necrotizing enterocolitis (NEC) models. Further clinical research is needed for exosome administration.
Area of Science:
- Neonatal research
- Gastroenterology
- Biomedical science
Background:
- Human breast milk (HBM) contains exosomes that protect against necrotizing enterocolitis (NEC).
- Pasteurization of donor milk may compromise its beneficial components.
- This study examines the impact of raw and pasteurized HBM exosomes on intestinal inflammation.
Purpose of the Study:
- To evaluate the therapeutic potential of exosomes from raw and pasteurized HBM in mitigating intestinal inflammation.
- To compare the efficacy of raw versus pasteurized HBM-derived exosomes in preclinical models of NEC.
Main Methods:
- Exosomes were isolated from HBM and characterized using western blot, nanoparticle tracking analysis, and transmission electron microscopy.
- Mouse intestine organoids and in vivo NEC models (hypoxia, gavage feeding, LPS) were used to assess exosome effects.
- Statistical analysis involved one-way ANOVA with Bonferroni post-test.
Main Results:
- Both raw and pasteurized HBM exosomes demonstrated anti-inflammatory effects in organoid models.
- In vivo, HBM exosomes (both raw and pasteurized) ameliorated NEC-induced mucosal injury, inflammation, and mucus overproduction.
- No significant difference was observed in the efficacy of raw versus pasteurized HBM exosomes.
Conclusions:
- Exosomes from both raw and pasteurized human breast milk equally reduce intestinal damage in NEC models.
- The findings suggest exosome administration as a potential therapeutic strategy for NEC.
- Further clinical investigation is warranted to explore exosome application in patient care.
Background:
Human breast milk (HBM), which contains an abundant supply of exosomes, is known to prevent necrotizing enterocolitis (NEC). Preterm infants are commonly given pasteurized donor milk when HBM is unavailable. However, pasteurization can disrupt its components. This study investigates the effects of both raw and pasteurized HBM-derived exosomes on intestinal inflammation.
Methods:
HBM exosomes were isolated and characterized by positive CD63 and negative calnexin markers from western blot, nanoparticle tracking analysis and transmission electron microscopy. Mouse intestine organoids were established and treated with exosomes from raw or pasteurized HBM in healthy and injury conditions. Following ethical approval (#44032), mice pups were randomly assigned to (1) breastfed control; (2) NEC; (3) NEC receiving raw HBM exosomes; (4) NEC receiving pasteurized HBM exosomes. NEC was induced by hypoxia, gavage feeding and lipopolysaccharide (LPS). Ileum was evaluated. Data were analyzed using one-way ANOVA with Bonferroni post-test.
Results:
Both raw and pasteurized HBM exosomes decreased inflammation in hypoxia and LPS-treated organoids compared to control. In vivo, NEC-induced mucosal injury, inflammation and mucous production were improved by raw and pasteurized HBM-derived exosomes.
Conclusions:
Exosomes derived from raw and pasteurized HBM equally reduced intestinal damage. Exosome administration in clinical practice requires further investigation.
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