Intracellular retention of interleukin-6 abrogates signaling

J Biol Chem. 1993 Oct 15;268(29):22084-91.

Abstract

Three forms of interleukin-6 (IL-6) have been constructed and stably transfected into human hepatoma cells (HepG2). Wild type IL-6 containing a signal peptide was rapidly secreted as a biologically active protein. IL-6 lacking the signal peptide accumulated within the cytoplasm of transfected cells. Surprisingly, IL-6 carrying a COOH-terminal extension of the amino acids Lys-Asp-Glu-Leu (KDEL) was not completely retained in the endoplasmic reticulum (ER). Complete retention in the ER was achieved when the 14 COOH-terminal amino acids of protein disulfide isomerase which include the KDEL signal were added to the COOH terminus of IL-6. This finding clearly demonstrates that the addition of the protein sorting signal KDEL alone is not sufficient for full retention of IL-6 in the ER. IL-6 accumulated in the cytoplasm and IL-6 retained in the ER failed to induce liver-specific acute-phase protein synthesis in the host cells, indicating that there is no intracellular role for IL-6 in signal transduction. Retention of IL-6 in the ER led to the prevention of surface expression of the IL-6 receptor protein gp80, making these cells unresponsive to IL-6. This phenomenon can be exploited in the future to generate transgenic animals which will become completely cytokine unresponsive in the tissues in which they express an ER retained cytokine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Base Sequence
  • Cytoplasm / metabolism
  • DNA, Complementary
  • Endoplasmic Reticulum / metabolism
  • Humans
  • Interleukin-6 / metabolism*
  • Isomerases / metabolism
  • Molecular Sequence Data
  • Protein Disulfide-Isomerases
  • Recombinant Fusion Proteins / metabolism
  • Signal Transduction*
  • Subcellular Fractions / metabolism
  • Tumor Cells, Cultured

Substances

  • DNA, Complementary
  • Interleukin-6
  • Recombinant Fusion Proteins
  • Isomerases
  • Protein Disulfide-Isomerases