Exosomal circRNAs contribute to intestinal development via the VEGF signalling pathway in human term and preterm colostrum

Aging (Albany NY). 2021 Apr 4;13(8):11218-11233. doi: 10.18632/aging.202806. Epub 2021 Apr 4.

Abstract

Human breast milk (HBM) provides essential nutrients for newborn growth and development, and contains a variety of biologically active ingredients that can affect gastrointestinal tract and immune system development in breastfed infants. HBM also contains mRNAs, microRNAs and lncRNAs, most of which are encapsulated in milk-derived exosomes and exhibit various important infant development related biological functions. While previous studies have shown that exosomal circRNAs are involved in the intestinal epithelial cells' proliferation and repair. However, the effect of HBM exosomal circRNAs on intestinal development is not clear. In this study, we identified 6756 circRNAs both in preterm colostrum (PC) and term colostrum (TC), of which 66 were upregulated, and 42 were downregulated (|fold change>2|, p < 0.05) in PC. Pathway analysis showed that the VEGF signalling pathway was involved, and network analysis revealed that the differentially expressed circRNAs bound various miRNAs. Further analyses showed that has_circRNA_405708 and has_circRNA_104707 were involved in the VEGF signalling pathway, and that they all bound various mirRNAs. Exosomes found in preterm colostrum (PC) and term colostrum (TC) promoted VEGF protein expression and induced the proliferation and migration of small intestinal epithelial cells (FHCs). Exosomal circRNAs found in human colostrum (HC) binding to related miRNAs may regulate VEGF signalling, and intestinal development.

Keywords: VEGF signaling pathway; circRNAs; exosome; human colostrum (HC); intestine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Breast Feeding
  • Cell Line
  • Cell Movement / genetics
  • Cell Proliferation / genetics
  • Child Development
  • Colostrum / cytology
  • Colostrum / metabolism*
  • Culture Media / metabolism
  • Epithelial Cells / physiology
  • Exosomes / metabolism
  • Female
  • Gene Expression Regulation, Developmental
  • Gestational Age
  • Humans
  • Infant, Newborn
  • Infant, Premature / growth & development
  • Intestines / growth & development*
  • Maternal Age
  • MicroRNAs / metabolism
  • Pregnancy
  • RNA, Circular / isolation & purification
  • RNA, Circular / metabolism*
  • Signal Transduction / genetics*
  • Vascular Endothelial Growth Factor A / metabolism*
  • Young Adult

Substances

  • Culture Media
  • MicroRNAs
  • RNA, Circular
  • VEGFA protein, human
  • Vascular Endothelial Growth Factor A