Effect of Lactobacillus brevis KB290 on the cell-mediated cytotoxic activity of mouse splenocytes: a DNA microarray analysis

Br J Nutr. 2013 Nov 14;110(9):1617-29. doi: 10.1017/S0007114513000767. Epub 2013 Apr 2.

Abstract

Lactic acid bacteria confer a variety of health benefits. Here, we investigate the mechanisms by which Lactobacillus brevis KB290 (KB290) enhances cell-mediated cytotoxic activity. Female BALB/c mice aged 9 weeks were fed a diet containing KB290 (3 × 10(9) colony-forming units/g) or starch for 1 d. The resulting cytotoxic activity of splenocytes against YAC-1 cells was measured using flow cytometry and analysed for gene expression using DNA microarray technology. KB290 enhanced the cell-mediated cytotoxic activity of splenocytes. DNA microarray analysis identified 327 up-regulated and 347 down-regulated genes that characterised the KB290 diet group. The up-regulated genes were significantly enriched in Gene Ontology terms related to immunity, and, especially, a positive regulation of T-cell-mediated cytotoxicity existed among these terms. Almost all the genes included in the term encoded major histocompatibility complex (MHC) class I molecules involved in the presentation of antigen to CD8(+) cytotoxic T cells. Marco and Signr1 specific to marginal zone macrophages (MZM), antigen-presenting cells, were also up-regulated. Flow cytometric analysis confirmed that the proportion of MZM was significantly increased by KB290 ingestion. Additionally, the over-represented Kyoto Encyclopedia of Genes and Genomes pathways among the up-regulated genes were those for natural killer (NK) cell-mediated cytotoxicity and antigen processing and presentation. The results for the selected genes associated with NK cells and CD8(+) cytotoxic T cells were confirmed by quantitative RT-PCR. These results suggest that enhanced cytotoxic activity could be caused by the activation of NK cells and/or of CD8(+) cytotoxic T cells stimulated via MHC class I presentation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigen-Presenting Cells / metabolism
  • CD8-Positive T-Lymphocytes / metabolism*
  • Cell Adhesion Molecules / metabolism
  • Cell Line, Tumor
  • Cytotoxicity, Immunologic*
  • Female
  • Flow Cytometry
  • Gene Expression
  • Histocompatibility Antigens Class I / genetics
  • Histocompatibility Antigens Class I / metabolism*
  • Killer Cells, Natural / metabolism
  • Lectins, C-Type / metabolism
  • Levilactobacillus brevis / immunology*
  • Lymphoma / immunology*
  • Macrophages / metabolism
  • Mice
  • Mice, Inbred BALB C
  • Microarray Analysis
  • Receptors, Cell Surface / metabolism
  • Receptors, Immunologic / metabolism
  • Spleen / cytology
  • Spleen / immunology*
  • T-Lymphocytes, Cytotoxic / metabolism*
  • Up-Regulation

Substances

  • Cell Adhesion Molecules
  • DC-specific ICAM-3 grabbing nonintegrin
  • Histocompatibility Antigens Class I
  • Lectins, C-Type
  • Marco protein, mouse
  • Receptors, Cell Surface
  • Receptors, Immunologic