The SCL gene product is regulated by and differentially regulates cytokine responses during myeloid leukemic cell differentiation

Proc Natl Acad Sci U S A. 1993 Aug 15;90(16):7864-8. doi: 10.1073/pnas.90.16.7864.

Abstract

Differentiation induction in murine M1 leukemia cells by interleukin 6 (IL-6), leukemia inhibitory factor (LIF), and oncostatin M (OSM) is postulated to occur via a common receptor chain, gp130. In this study, growth factor-induced differentiation of M1 cells was accompanied by a late and persistent decrease in levels of mRNA and protein for a helix-loop-helix transcription factor, the SCL gene product. To evaluate whether reduced SCL expression was instrumental in monocyte differentiation, an SCL cDNA expression vector was introduced into M1 cells to obtain cell lines in which overexpression of SCL mRNA and protein was enforced. This resulted in a reduction in cells differentiating in response to LIF and OSM but not in response to IL-6. Scatchard analysis indicated that both parental and SCL-transfected cell lines exhibited similar receptor numbers and receptor affinities for LIF, OSM, and IL-6, suggesting that the differential responsiveness was not due to selective receptor down-modulation. Thus, these data implicate SCL in monocytic differentiation and provide evidence for differential receptor signaling pathways despite utilization of a common gp130 subunit by all three receptors.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Basic Helix-Loop-Helix Transcription Factors
  • Cell Differentiation / drug effects
  • Cytokines / metabolism
  • Cytokines / pharmacology*
  • DNA-Binding Proteins / biosynthesis
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • Dose-Response Relationship, Drug
  • Genetic Vectors
  • Growth Inhibitors / metabolism
  • Growth Inhibitors / pharmacology
  • Interleukin-6 / metabolism
  • Interleukin-6 / pharmacology
  • Kinetics
  • Leukemia Inhibitory Factor
  • Leukemia, Experimental
  • Lymphokines / metabolism
  • Lymphokines / pharmacology
  • Mice
  • Oncostatin M
  • Peptides / metabolism
  • Peptides / pharmacology
  • Proto-Oncogene Proteins*
  • Retroviridae
  • T-Cell Acute Lymphocytic Leukemia Protein 1
  • Transcription Factors / metabolism*
  • Transfection
  • Tumor Cells, Cultured

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • Cytokines
  • DNA-Binding Proteins
  • Growth Inhibitors
  • Interleukin-6
  • Leukemia Inhibitory Factor
  • Lif protein, mouse
  • Lymphokines
  • Osm protein, mouse
  • Peptides
  • Proto-Oncogene Proteins
  • T-Cell Acute Lymphocytic Leukemia Protein 1
  • Tal1 protein, mouse
  • Transcription Factors
  • Oncostatin M