Characterization and regulation of interleukin-4 receptor in adult T-cell leukemia cells

Eur J Haematol. 1996 Apr;56(4):241-7. doi: 10.1111/j.1600-0609.1996.tb01936.x.

Abstract

We studied the expression of the receptor of interleukin (IL-4), one of the T cell growth factors, on fresh peripheral blood leukemic cells from adult T-cell leukemia (ATL) patients. Flow cytofluorometric analysis with a monoclonal antibody to the IL-4 receptor (IL-4R) were used to investigate whether expression of IL-4R on ATL cells is different from that on normal lymphocytes and other types of leukemic cells. Leukemic cells from acute type ATL patients synthesize IL-4R without stimulation, at levels much higher than normal resting lymphocytes and other types of leukemic cells. Furthermore, leukemic cells from acute type ATL showed higher IL-4R expression than that of chronic type ATL or human T-cell leukemia virus type I carriers. In addition, there was correlation between expression of IL-4R on the cell surface and the proliferative response to IL-4. Both IL-4 and IL-2 induced upregulation of IL-4R on activated normal T cells but not on ATL cells. These results suggest that abnormal expression of IL-4R may display different biological activities in ATL compared with other types of leukemia. Furthermore, the high expression of IL-4R in ATL may be involved in the proliferation of leukemic cells and the leukemogenesis in this disease.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antigens, CD / biosynthesis*
  • Antigens, CD / genetics
  • Cell Transformation, Neoplastic
  • Flow Cytometry
  • Gene Expression Regulation, Leukemic*
  • Humans
  • Interferon-gamma / pharmacology
  • Interleukin-2 / pharmacology
  • Interleukin-4 / pharmacology
  • Leukemia / genetics
  • Leukemia / metabolism
  • Leukemia / pathology
  • Leukemia-Lymphoma, Adult T-Cell / genetics
  • Leukemia-Lymphoma, Adult T-Cell / metabolism*
  • Leukemia-Lymphoma, Adult T-Cell / pathology
  • Lymphocyte Activation / drug effects
  • Lymphocytes / drug effects
  • Lymphocytes / metabolism*
  • Neoplasm Proteins / biosynthesis*
  • Neoplasm Proteins / genetics
  • Neoplastic Stem Cells / drug effects
  • Neoplastic Stem Cells / metabolism*
  • Receptors, Interleukin / biosynthesis*
  • Receptors, Interleukin / genetics
  • Receptors, Interleukin-4
  • Recombinant Proteins / pharmacology
  • Tumor Cells, Cultured

Substances

  • Antigens, CD
  • Interleukin-2
  • Neoplasm Proteins
  • Receptors, Interleukin
  • Receptors, Interleukin-4
  • Recombinant Proteins
  • Interleukin-4
  • Interferon-gamma