Suppression of T lymphocyte activation by 3-chloro-1,2-propanediol mono- and di-palmitate esters in vitro

Toxicol In Vitro. 2018 Sep:51:54-62. doi: 10.1016/j.tiv.2018.05.002. Epub 2018 May 4.

Abstract

This study investigated whether and how 3-chloro-1,2-propanediol (3-MCPD) fatty acid esters, a group of food contaminants formed during processing, might inhibit the immune system through suppressing T lymphocyte activation for the first time. Three 3-MCPD esters including 1-palmitoyl-3-chloropropanediol (1-pal), 2-palmitoyl-3-chloropropanediol (2-pal), and1,2-dipalmitoyl-3-chloropropanediol (dipal) were selected as the probe compounds to test the possible effects of fatty acid structure on their potential immune inhibitory effect. The results showed that 1-pal and 2-pal, but not dipal, significantly suppressed ConA-induced T lymphocyte proliferation, cell cycle activity, Th1 and Th2 cytokine secretion, CD4+ T cell populations, and the ratio of CD4+/CD8+ T cells under the experimental conditions. Moreover, Western blotting and immunofluorescence analyses revealed that 1-pal and 2-pal could inhibit the activation of ConA-stimulated mitogen-activated protein kinase (MAPK) and nuclear factor-kappa B (NF-κB) signaling pathways. In addition, 1-pal significantly suppressed DNFB-induced delayed-type hyper sensitivity (DTH) reaction characterized by the increased ear thickness and IFN-γ production in mice. These observations indicated that 3-MCPD esters exerted a negative effect on T lymphocyte-mediated immunity, and the immunosuppressive activities of 3-MCPD monopalmitates were stronger than 3-MCPD dipalmitate.

Keywords: 3-MCPD palmitate esters; DTH reaction; Immunosuppressive; MAPK; NF-қB; T lymphocyte.

MeSH terms

  • Animals
  • Cell Cycle / drug effects
  • Cell Proliferation / drug effects
  • Cells, Cultured
  • Cytokines / blood
  • Cytokines / metabolism
  • Dinitrofluorobenzene
  • Esters
  • Female
  • Hypersensitivity, Delayed / blood
  • Hypersensitivity, Delayed / immunology
  • Immunosuppressive Agents / toxicity*
  • Lymphocyte Activation / drug effects
  • Mice, Inbred BALB C
  • Mitogen-Activated Protein Kinases / metabolism
  • NF-kappa B / metabolism
  • Palmitates / toxicity*
  • Propylene Glycols / toxicity*
  • Spleen / cytology
  • T-Lymphocytes / drug effects*
  • T-Lymphocytes / metabolism

Substances

  • Cytokines
  • Esters
  • Immunosuppressive Agents
  • NF-kappa B
  • Palmitates
  • Propylene Glycols
  • Dinitrofluorobenzene
  • Mitogen-Activated Protein Kinases