Supplementation of p40, a Lactobacillus rhamnosus GG-derived protein, in early life promotes epidermal growth factor receptor-dependent intestinal development and long-term health outcomes

Mucosal Immunol. 2018 Sep;11(5):1316-1328. doi: 10.1038/s41385-018-0034-3. Epub 2018 Jun 6.

Abstract

The beneficial effects of the gut microbiota on growth in early life are well known. However, knowledge about the mechanisms underlying regulating intestinal development by the microbiota is limited. p40, a Lactobacillus rhamnosus GG-derived protein, transactivates epidermal growth factor receptor (EGFR) in intestinal epithelial cells for protecting the intestinal epithelium against injury and inflammation. Here, we developed p40-containing pectin/zein hydrogels for targeted delivery of p40 to the small intestine and the colon. Treatment with p40-containing hydrogels from postnatal day 2 to 21 significantly enhanced bodyweight gain prior to weaning and functional maturation of the intestine, including intestinal epithelial cell proliferation, differentiation, and tight junction formation, and IgA production in early life in wild-type mice. These p40-induced effects were abolished in mice with specific deletion of EGFR in intestinal epithelial cells, suggesting that transactivation of EGFR in intestinal epithelial cells may mediate p40-regulated intestinal development. Furthermore, neonatal p40 treatment reduced the susceptibility to intestinal injury and colitis and promoted protective immune responses, including IgA production and differentiation of regulatory T cells, in adult mice. These findings reveal novel roles of neonatal supplementation of probiotic-derived factors in promoting EGFR-mediated maturation of intestinal functions and innate immunity, which likely promote long-term beneficial outcomes.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bacterial Proteins / pharmacology*
  • Cell Differentiation / drug effects
  • Cell Differentiation / immunology
  • Cell Proliferation / drug effects
  • Epithelial Cells / drug effects*
  • Epithelial Cells / immunology
  • ErbB Receptors / metabolism*
  • Female
  • Hydrogels / pharmacology
  • Immunity, Innate / drug effects
  • Immunity, Innate / immunology
  • Immunoglobulin A / immunology
  • Intestinal Mucosa / drug effects*
  • Lacticaseibacillus rhamnosus / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Probiotics / pharmacology
  • T-Lymphocytes, Regulatory / drug effects
  • T-Lymphocytes, Regulatory / immunology
  • Tight Junctions / drug effects
  • Tight Junctions / immunology
  • Time
  • Transcriptional Activation / drug effects
  • Transcriptional Activation / immunology

Substances

  • Bacterial Proteins
  • Hydrogels
  • Immunoglobulin A
  • EGFR protein, mouse
  • ErbB Receptors