Interleukin-2 (IL-2) receptor alpha, beta and gamma subunit expression as a function of B-cell lineage ontogeny: the use of IL-2-PE66(4Glu) to characterize internalization via IL-2 receptor subunits

Scand J Immunol. 1997 Aug;46(2):129-36. doi: 10.1046/j.1365-3083.1997.d01-101.x.

Abstract

Interleukin-2 (IL-2) is a pluripotent cytokine which plays a crucial role in the immune system response. Although the IL-2/IL-2 receptor (IL-2R) system has been well characterized in cells of the T lineage it is less known in B lymphocytes. The authors therefore studied the expression of the IL-2R alpha, beta and gamma subunits in human B-cell lines at different stages of maturation, by the polymerase chain reaction technique. The authors found that the alpha and beta subunits are expressed in the final stages of B-cell lineage maturation, whereas the gamma subunit is constitutively expressed during B-lymphocyte differentiation. The results indicate that the IL-2/IL-2R system, most probably, does not have a role in the early stages of B-cell differentiation, but may be involved only in the final stages of B-cell lineage ontogeny. Moreover, the ability of the different forms of IL-2R to internalize the IL-2 ligand was investigated, using the chimeric protein IL-2-PE66(4Glu). Cell lines bearing the alphagamma, betagamma and alpha betagamma forms of IL-2R were inhibited by the chimeric protein, while those bearing the gamma subunit alone did not respond to the chimera. Thus, internalization of IL-2 is most likely mediated via the alphagamma form of the IL-2R, as shown here for the first time, as well as through the betagamma and alpha betagamma IL-2R forms. However, IL-2 cannot be internalized through the IL-2R gamma subunit alone.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • B-Lymphocytes / cytology*
  • B-Lymphocytes / drug effects
  • B-Lymphocytes / metabolism
  • Cell Differentiation / physiology
  • Cell Line
  • Cell Lineage / physiology
  • Cells, Cultured
  • DNA Primers / chemistry
  • Endocytosis / physiology*
  • Exotoxins / pharmacology*
  • Humans
  • Interleukin-2 / metabolism
  • Interleukin-2 / pharmacology*
  • Ligands
  • Polymerase Chain Reaction
  • RNA, Messenger / metabolism
  • Receptors, Interleukin-2 / classification
  • Receptors, Interleukin-2 / genetics
  • Receptors, Interleukin-2 / metabolism*
  • Recombinant Fusion Proteins*
  • Recombinant Proteins / pharmacology

Substances

  • DNA Primers
  • Exotoxins
  • Interleukin-2
  • Ligands
  • RNA, Messenger
  • Receptors, Interleukin-2
  • Recombinant Fusion Proteins
  • Recombinant Proteins
  • interleukin 2-PE66(4Glu) protein, recombinant