Milk-derived exosomes (MDEs) have a different biological effect on normal fetal colon epithelial cells compared to colon tumor cells in a miRNA-dependent manner

J Transl Med. 2019 Sep 30;17(1):325. doi: 10.1186/s12967-019-2072-3.

Abstract

Background: Breastfeeding is the ideal source of infant nutrition. Human milk consists not only of nutrients but also biologically active components. Among these latter compounds, exosomes contain proteins, lipids, mRNAs and miRNAs.

Methods: To elucidate the biological effects of milk-derived exosomes (MDEs) on normal colonic epithelial cells compared to colonic tumor cells, we incubated cells with MDEs. MDEs were able to enter into normal and tumor cells and change their miRNA expression profiles. Proliferation, cell morphology and protein expression were analyzed in these cells.

Results: Human milk-derived exosomes induced proliferation- and epithelial mesenchymal transformation-related changes, such as collagen type I and twist expression, in normal but not in tumor cells. PTEN, a target of miRNA-148a, was downregulated in normal but not in tumor cells following incubation with MDEs. Moreover, miRNA-148a-3p knockdown cells were used to demonstrate the importance of miRNA in the effect of exosomes on cell proliferation and protein expression. MDEs inhibited proliferation and DNMT1 expression in cells with knockdown of miRNA-148a.

Conclusions: In conclusion, the positive effect of exosomes on normal cells without affecting tumor cells may presents an aspect of their safety when considering it use as a nutritional supplement to infant formula.

Keywords: Colon cells; Exosomes; Milk; miRNA.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Cattle
  • Cell Line, Tumor
  • Cell Proliferation
  • Cell Shape
  • Colon / cytology*
  • Colonic Neoplasms / pathology*
  • DNA (Cytosine-5-)-Methyltransferase 1 / genetics
  • DNA (Cytosine-5-)-Methyltransferase 1 / metabolism
  • Down-Regulation / genetics
  • Epithelial Cells / cytology*
  • Exosomes / metabolism*
  • Fetus / cytology*
  • Humans
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Milk, Human / metabolism*
  • PTEN Phosphohydrolase / genetics
  • PTEN Phosphohydrolase / metabolism
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism

Substances

  • MicroRNAs
  • RNA, Messenger
  • DNA (Cytosine-5-)-Methyltransferase 1
  • PTEN Phosphohydrolase