Binding and internalization of the 163-171 fragment of human IL-1 beta

Cytokine. 1992 May;4(3):201-4. doi: 10.1016/1043-4666(92)90056-w.

Abstract

The mechanisms of cell association of the human interleukin (IL-1 beta) immunostimulatory fragment 163-171 have been studied. The fragment was able to associate abundantly to both IL-1R- and IL-1R+ cells. Binding was strictly temperature dependent, was not saturable and could be inhibited by excess amounts of unlabelled 163-171 peptide but not by IL-1 beta, suggesting that the 163-171 fragment is not an IL-1R-binding domain of IL-1 beta. The fragment is readily internalized by cells by a cytochalasin-insensitive mechanism and it localizes mainly in the cytoplasm. It is concluded that the active domain 163-171 of IL-1 beta can be taken up by cells through a receptor-independent, temperature-dependent mechanisms and that its ability to activate cellular functions is based on IL-1R-independent intracellular pathways.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Binding, Competitive
  • Cytoplasm
  • Diffusion
  • Humans
  • Interleukin-1 / metabolism*
  • Interleukin-1 / pharmacology
  • Interleukin-1beta
  • Mice
  • Molecular Sequence Data
  • Peptide Fragments / metabolism*
  • Peptide Fragments / pharmacology
  • Protein Binding
  • Receptors, Immunologic / metabolism
  • Receptors, Interleukin-1
  • Signal Transduction
  • Temperature
  • Tumor Cells, Cultured / metabolism

Substances

  • Interleukin-1
  • Interleukin-1beta
  • Peptide Fragments
  • Receptors, Immunologic
  • Receptors, Interleukin-1
  • interleukin-1beta (163-171)