Epithelial cell proliferation arrest induced by lactate and acetate from Lactobacillus casei and Bifidobacterium breve

PLoS One. 2013 Apr 30;8(4):e63053. doi: 10.1371/journal.pone.0063053. Print 2013.

Abstract

In an attempt to identify and characterize how symbiotic bacteria of the gut microbiota affect the molecular and cellular mechanisms of epithelial homeostasis, intestinal epithelial cells were co-cultured with either Lactobacillus or Bifidobacterium as bona fide symbionts to examine potential gene modulations. In addition to genes involved in the innate immune response, genes encoding check-point molecules controlling the cell cycle were among the most modulated in the course of these interactions. In the m-ICcl2 murine cell line, genes encoding cyclin E1 and cyclin D1 were strongly down regulated by L. casei and B. breve respectively. Cell proliferation arrest was accordingly confirmed. Short chain fatty acids (SCFA) were the effectors of this modulation, alone or in conjunction with the acidic pH they generated. These results demonstrate that the production of SCFAs, a characteristic of these symbiotic microorganisms, is potentially an essential regulatory effector of epithelial proliferation in the gut.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetates / metabolism*
  • Acetates / pharmacology
  • Animals
  • Bifidobacterium / metabolism*
  • Cell Cycle Checkpoints / drug effects
  • Cell Cycle Checkpoints / genetics
  • Cell Line
  • Cell Proliferation / drug effects
  • Cyclin D1 / genetics
  • Cyclin D1 / metabolism
  • Cyclin E / genetics
  • Cyclin E / metabolism
  • Epithelial Cells / drug effects
  • Epithelial Cells / metabolism*
  • Epithelial Cells / microbiology*
  • Gene Expression Regulation / drug effects
  • Humans
  • Hydrogen-Ion Concentration
  • Intestinal Mucosa / metabolism
  • Intestinal Mucosa / microbiology
  • Lactic Acid / metabolism*
  • Lactic Acid / pharmacology
  • Lacticaseibacillus casei / metabolism*
  • Mice
  • Microbiota
  • Symbiosis

Substances

  • Acetates
  • Cyclin E
  • Cyclin D1
  • Lactic Acid

Grants and funding

This work was supported by the European Research Council and from grants from Danone Research and Yakult Research. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.