Isolation and characterization of lymphokine cDNA clones encoding mouse and human IgA-enhancing factor and eosinophil colony-stimulating factor activities: relationship to interleukin 5

Proc Natl Acad Sci U S A. 1987 Nov;84(21):7388-92. doi: 10.1073/pnas.84.21.7388.

Abstract

Conditioned medium from the Con A-treated mouse helper T-cell clone Ly1+2-/9 contains activities that enhance the production of IgA by mouse B cells and induce human cord blood cells to form eosinophil colonies. We have isolated a cDNA sequence that expresses IgA-enhancing factor and eosinophil colony-stimulating factor activities from a cDNA library prepared from activated Ly1+2-/9 cells. Based on homology with the mouse cDNA sequence, a human cDNA sequence coding for an interleukin with IgA-enhancing factor and eosinophil colony-stimulating factor activities was isolated from a cDNA library prepared from a human T-cell clone stimulated with anti-T3 antibody and phorbol 12-myristate 13-acetate. DNA sequence analyses revealed that mouse and human cDNA clones encode proteins of 133 and 134 amino acids, respectively, that are identical to cDNA clones encoding the T-cell replacing factor I and B-cell growth factor II activities. These results establish that a single cDNA clone encodes a protein that acts as a growth and differentiation factor for both B cells and eosinophils.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Bone Marrow Cells
  • Cell Line
  • Cloning, Molecular*
  • Colony-Stimulating Factors / genetics*
  • DNA / isolation & purification*
  • DNA Restriction Enzymes
  • Eosinophils
  • Humans
  • Interleukin-5
  • Interleukins / genetics*
  • Lymphokines / genetics*
  • Mice
  • Molecular Sequence Data
  • Prostatic Secretory Proteins*
  • RNA, Messenger / genetics
  • RNA, Messenger / isolation & purification
  • T-Lymphocytes

Substances

  • Colony-Stimulating Factors
  • Interleukin-5
  • Interleukins
  • Lymphokines
  • Prostatic Secretory Proteins
  • RNA, Messenger
  • beta-microseminoprotein
  • immunoglobulin-binding factors
  • DNA
  • DNA Restriction Enzymes