The differential organogenesis and functionality of two liver-draining lymph nodes in mice

J Autoimmun. 2017 Nov:84:109-121. doi: 10.1016/j.jaut.2017.08.005. Epub 2017 Sep 5.

Abstract

The liver is an immunological organ. However, fundamental knowledge concerning liver-draining lymph nodes (LNs), which have been newly identified in mice as the portal and celiac LNs, is still lacking. Here, we revealed that the portal LN and celiac LN drain liver lymph through different lymphatic vessels. Although both the portal LN and celiac LN possess typical structures, they have different cell compositions. Interestingly, these two LNs form at different times during fetal development. Moreover, the organogenesis of the celiac LN, but not the portal LN, is controlled by the transcription factor NFIL3. Furthermore, the portal LN and celiac LN also perform different functions. The celiac LN is the predominant site of liver antiviral immune responses, whereas the portal LN functions in the in situ induction of dietary antigen-specific regulatory T cells. In conclusion, the portal LN and celiac LN are two independent liver-draining LNs with different organogenesis histories and separate functions in maintaining immune homeostasis in the liver.

Keywords: Celiac lymph node; Immunotolerance; Organogenesis; Portal lymph node; Viral infection.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Basic-Leucine Zipper Transcription Factors / genetics
  • Celiac Artery / immunology*
  • Celiac Artery / pathology
  • Humans
  • Immune Tolerance
  • Immunity
  • Interleukin Receptor Common gamma Subunit / genetics
  • Liver / immunology*
  • Lymph Nodes / immunology*
  • Lymph Nodes / pathology
  • Lymphatic Vessels / pathology*
  • Lymphocytic Choriomeningitis / immunology*
  • Lymphocytic choriomeningitis virus / immunology*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Organogenesis
  • Portal Vein / immunology*
  • Portal Vein / pathology

Substances

  • Basic-Leucine Zipper Transcription Factors
  • Il2rg protein, mouse
  • Interleukin Receptor Common gamma Subunit
  • Nfil3 protein, mouse