Interleukin-9 induces 24P3 lipocalin gene expression in murine T cell lymphomas

Eur Cytokine Netw. 2001 Mar;12(1):154-61.

Abstract

Interleukin-9 (IL-9) is a Th2 cytokine whose overexpression is associated with asthma and T cell lymphomagenesis. All the IL-9 activities studied so far are mediated by a specific hemopoietin receptor that activates a Jak/STAT pathway. Searching for genes specifically modulated by IL-9, we observed that the 24P3 mRNA is strongly upregulated in BW5147 T lymphoma cells upon IL-9 stimulation. 24P3 is a member of the lipocalin family, and has been reported to bind N-formyl-Met-Leu-Phe, a potent neutrophil chemoattractant, and possibly other lipophilic mediators of inflammation. A similar 24P3 induction was observed in other T cell lymphomas (EL4 and TH201) in response to IL-9, as well as in EL4 cells stimulated with IL-6 or IL-1. By contrast, other IL-9-responsive cells such as mast cell line MC9 and B cell lymphoma A20 showed no 24P3 induction upon IL-9 stimulation. Experiments using IL-9R mutants indicated that STAT transcription factors, particularly STAT3, are involved in this process. However, 24P3 gene induction was slow, reaching a plateau from 36 to 72 hours after stimulation and was inhibited if cells were treated with cycloheximide during the first 8 hours of IL-9 stimulation, suggesting an indirect induction requiring new protein synthesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute-Phase Proteins / genetics*
  • Animals
  • Base Sequence
  • Blotting, Northern
  • Carrier Proteins / genetics*
  • DNA Primers
  • Gene Expression Regulation, Neoplastic / physiology*
  • Interleukin-9 / physiology*
  • Lipocalin-2
  • Lipocalins
  • Lymphoma, T-Cell / genetics*
  • Lymphoma, T-Cell / pathology
  • Mice
  • Nucleic Acid Hybridization
  • Oncogene Proteins / genetics*
  • RNA, Messenger / genetics
  • Reverse Transcriptase Polymerase Chain Reaction
  • Thymus Neoplasms / genetics*
  • Thymus Neoplasms / pathology
  • Transcription Factors / physiology
  • Transcriptional Activation
  • Tumor Cells, Cultured

Substances

  • Acute-Phase Proteins
  • Carrier Proteins
  • DNA Primers
  • Interleukin-9
  • Lipocalin-2
  • Lipocalins
  • Oncogene Proteins
  • RNA, Messenger
  • Transcription Factors
  • Lcn2 protein, mouse