Constitutive association of JAK1 and STAT5 in pro-B cells is dissolved by interleukin-4-induced tyrosine phosphorylation of both proteins

FEBS Lett. 1998 Nov 13;439(1-2):71-4. doi: 10.1016/s0014-5793(98)01341-6.

Abstract

The bipartite human interleukin-4 (IL-4) receptor was functionally expressed in murine pro-B cells and activated by human IL-4 to evoke intracellular signaling. Mutual association of signal transducing proteins within the receptor complex was then studied in dependence of ligand stimulation. Besides ligand-induced receptor heterodimerization and contacts of the two IL-4 receptor subunits alpha and gamma with Janus kinases JAK1 and JAK3 a prominent constitutive binding between JAK1 and signal transducer and activator of transcription STAT5 was detected. Since both these proteins become phosphorylated in response to IL-4 receptor stimulation, the influence of tyrosine phosphorylation on their mutual contact was analyzed. Association of JAK1 and STAT5 was found to occur exclusively between unphosphorylated proteins.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • B-Lymphocytes / drug effects
  • B-Lymphocytes / enzymology
  • B-Lymphocytes / metabolism*
  • Cell Line
  • DNA-Binding Proteins / metabolism*
  • Humans
  • Interleukin-4 / pharmacology*
  • Janus Kinase 1
  • Milk Proteins*
  • Phosphorylation / drug effects
  • Protein-Tyrosine Kinases / metabolism*
  • Receptors, Cytokine / metabolism
  • STAT5 Transcription Factor
  • Trans-Activators / metabolism*
  • Tyrosine / metabolism

Substances

  • DNA-Binding Proteins
  • Milk Proteins
  • Receptors, Cytokine
  • STAT5 Transcription Factor
  • Trans-Activators
  • Interleukin-4
  • Tyrosine
  • Protein-Tyrosine Kinases
  • JAK1 protein, human
  • Janus Kinase 1