Interleukin-15 increases hepatic regenerative activity

J Hepatol. 2006 Sep;45(3):410-8. doi: 10.1016/j.jhep.2006.04.008. Epub 2006 May 22.

Abstract

Background/aims: Interleukin-15 (IL-15) is expressed in many organs. It generally inhibits apoptosis and increases cellular proliferation and differentiation. However, IL-15's roles in liver are unknown. We aimed to determine if IL-15 influences hepatic integrity and regenerative activity.

Methods: Expression of IL-15 and its receptors was evaluated in several liver injury models, primary hepatocytes, and two liver cell lines. Effects of IL-15 on viability, proliferation, and apoptosis were assessed in cultured liver cells, and also in the livers of healthy mice.

Results: IL-15 and its receptors are expressed constitutively in healthy livers, and ligand expression is induced in injured livers. Cultured primary hepatocytes and liver cell lines express IL-15 and its receptors. Administration of IL-15 has minimal effects on cultured liver cells, but significantly up-regulates oval cell accumulation, cyclin mRNA expression, and mature hepatocyte replication in healthy mice. These effects are associated with focal hepatic inflammation and increased expression of TNF-alpha and IFN-gamma, but not with increased cell death or aminotransferase release.

Conclusions: IL-15 expression increases during liver injury and IL-15 treatment induces a wound healing-type response in healthy adult mice. These findings suggest that IL-15 may contribute to regenerative activity in damaged liver.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Cell Line
  • Cell Proliferation / drug effects
  • Cell Survival / drug effects
  • Cells, Cultured
  • Gene Expression Regulation / genetics
  • Hepatocytes / drug effects
  • Hepatocytes / metabolism
  • Inflammation
  • Interferon-gamma / genetics
  • Interferon-gamma / metabolism
  • Interleukin-15 / genetics*
  • Interleukin-15 / metabolism*
  • Interleukin-15 / pharmacology
  • Liver / drug effects
  • Liver / injuries
  • Liver / metabolism*
  • Liver / pathology
  • Liver Regeneration / genetics*
  • Liver Regeneration / physiology*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Obese
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Receptors, Interleukin-15 / genetics
  • Receptors, Interleukin-15 / metabolism
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / metabolism
  • Wound Healing

Substances

  • Interleukin-15
  • RNA, Messenger
  • Receptors, Interleukin-15
  • Tumor Necrosis Factor-alpha
  • Interferon-gamma