Human milk exosomes and their microRNAs survive digestion in vitro and are taken up by human intestinal cells

Mol Nutr Food Res. 2017 Nov;61(11). doi: 10.1002/mnfr.201700082. Epub 2017 Aug 15.

Abstract

Scope: Human milk exosomes provide a natural means of genetic material transfer to infants; however, the effect of gastric/pancreatic digestion milk exosomes stability and their microRNA content is largely unknown.

Methods and results: We took a simulated gastric/pancreatic digestion protocol to perform in vitro digestion of milk exosomes, explore intestinal epithelial uptake, and further elucidate microRNA responses to digestion at early-, mid-, late lactation by massive parallel sequencing. Both undigested and digested exosomes enter human intestinal crypt-like cells (HIEC), with evidence of nuclear localization. We identified 288 mature microRNAs from all 24 exosome samples, and an additional 610 at low abundance. A large number of synapse development- and immune-related microRNAs were identified. hsa-miR-22-3p was the most abundant microRNA, and the top 15 microRNAs contributed ∼11% of the sequencing reads. Upon digestion, the overall microRNA abundance in human milk exosomes was stable.

Conclusion: Our results for the first time reveal the survivability and complexity of human milk exosome microRNAs upon simulated gastric/pancreatic digestion, and the dynamics during lactation stages. The results suggest a previously underexplored area of infant response to genetic material in human milk exosomes.

Keywords: Exosome; Human milk; In vitro digestion; Intestine; MicroRNA.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Active Transport, Cell Nucleus
  • Adult
  • Base Sequence
  • Cell Line
  • Cells, Cultured
  • Digestion*
  • Enterocytes / cytology
  • Enterocytes / metabolism*
  • Exosomes / chemistry
  • Exosomes / metabolism*
  • Exosomes / ultrastructure
  • Female
  • Humans
  • Intestinal Absorption*
  • Lactation
  • MicroRNAs / chemistry
  • MicroRNAs / metabolism*
  • Microscopy, Electron, Scanning
  • Milk Proteins / chemistry
  • Milk Proteins / metabolism*
  • Milk, Human / chemistry
  • Milk, Human / metabolism*
  • Particle Size
  • Protein Stability
  • RNA Stability
  • Sequence Analysis, RNA
  • Young Adult

Substances

  • MIRN22 microRNA, human
  • MicroRNAs
  • Milk Proteins