Interleukin-10 expression is autoregulated at the transcriptional level in human and murine Kupffer cells

Hepatology. 1998 Jan;27(1):93-9. doi: 10.1002/hep.510270116.

Abstract

Interleukin 10 (IL-10) is known to downregulate immune responses. The regulation of IL-10 gene expression therefore determines the outcome of local immune reactions. We investigated time course and downregulation of IL-10 production in primary Kupffer's cells (KC), which are known to secrete IL-10 in response to endotoxin challenge. Human and murine KC were isolated by centrifugal elutriation and investigated for IL-10 gene expression by a two-step amplification procedure (reverse transcriptase-polymerase chain reaction [PCR] followed by T7-polymerase chain reaction). We show that IL-10 messenger ribonucleic acid (mRNA) showed a >450 fold increase in KC 2 hours after endotoxin challenge. IL-10 protein release from KC strictly depended on de novo protein synthesis. Endotoxin mediated increase in IL-10 gene expression was downregulated by exogenous (>350-fold reduction of IL-10 mRNA level), as well as endogenous IL-10 protein, showing a negative autoregulatory feedback loop. IL-10 receptor expression was found to be constitutive and functional in KC. Early expression of IL-10 in KC may be of functional relevance to the outcome of immune and inflammatory reactions in the liver sinusoid. The negative autoregulation of IL-10 expression may represent a mechanism to regain a state of functional responsiveness in the microenvironment towards new proinflammatory stimuli. In conclusion, autoregulatory downregulation of IL-10 expression in KC may account for important regulatory steps of local immune response in the liver sinusoid.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Endotoxins / pharmacology
  • Homeostasis / physiology*
  • Humans
  • Interleukin-10 / genetics*
  • Interleukin-10 / metabolism*
  • Interleukin-10 / pharmacology
  • Kinetics
  • Kupffer Cells / drug effects
  • Kupffer Cells / metabolism*
  • Mice
  • Mice, Inbred BALB C
  • RNA, Messenger / metabolism
  • Receptors, Interleukin / genetics
  • Transcription, Genetic*

Substances

  • Endotoxins
  • RNA, Messenger
  • Receptors, Interleukin
  • Interleukin-10