Direct effects of fermented cow's milk product with Lactobacillus paracasei CBA L74 on human enterocytes

Benef Microbes. 2018 Jan 29;9(1):165-172. doi: 10.3920/BM2017.0038. Epub 2017 Oct 25.

Abstract

Cow's milk fermented with Lactobacillus paracasei CBA L74 (FM-CBAL74) exerts a preventive effect against infectious diseases in children. We evaluated if this effect is at least in part related to a direct modulation of non-immune and immune defence mechanisms in human enterocytes. Human enterocytes (Caco-2) were stimulated for 48 h with FM-CBAL74 at different concentrations. Cell growth was assessed by colorimetric assay; cell differentiation (assessed by lactase expression), tight junction proteins (zonula occludens1 and occludin), mucin 2, and toll-like receptor (TRL) pathways were analysed by real-time PCR; innate immunity peptide synthesis, beta-defensin-2 (HBD-2) and cathelicidin (LL-37) were evaluated by ELISA. Mucus layer thickness was analysed by histochemistry. FMCBA L74 stimulated cell growth and differentiation, tight junction proteins and mucin 2 expression, and mucus layer thickness in a dose-dependent fashion. A significant stimulation of HBD-2 and LL-37 synthesis, associated with a modulation of TLR pathway, was also observed. FM-CBAL74 regulates non-immune and immune defence mechanisms through a direct interaction with the enterocytes. These effects could be involved in the preventive action against infectious diseases demonstrated by this fermented product in children.

Keywords: fermented foods; gut mucosa; infectious diseases; innate immunity; intestinal permeability.

MeSH terms

  • Antimicrobial Cationic Peptides / biosynthesis
  • Caco-2 Cells
  • Cathelicidins
  • Cell Differentiation / drug effects
  • Cell Proliferation / drug effects
  • Cultured Milk Products / microbiology*
  • Enterocytes / cytology
  • Enterocytes / drug effects*
  • Enterocytes / immunology
  • Enterocytes / ultrastructure
  • Gene Expression Regulation / drug effects
  • Humans
  • Lacticaseibacillus paracasei / physiology*
  • Mucin-2 / genetics
  • Occludin / genetics
  • Probiotics / pharmacology*
  • Tight Junctions / genetics
  • Tight Junctions / metabolism
  • Toll-Like Receptors / genetics
  • Zonula Occludens-1 Protein / genetics
  • beta-Defensins / biosynthesis

Substances

  • Antimicrobial Cationic Peptides
  • DEFB4A protein, human
  • MUC2 protein, human
  • Mucin-2
  • OCLN protein, human
  • Occludin
  • TJP1 protein, human
  • Toll-Like Receptors
  • Zonula Occludens-1 Protein
  • beta-Defensins
  • Cathelicidins