Interleukin-7 inhibits apoptosis of mouse malignant T-lymphoma cells by both suppressing the CPP32-like protease activation and inducing the Bcl-2 expression

Oncogene. 1996 Nov 21;13(10):2131-9.

Abstract

Mouse malignant T-lymphoma CS-21 cells grow in vitro in the presence of CA-12 lymph node stromal cells, but they undergo apoptotic cell death when separated from CA-12 stromal cells. In the course of examining the nursing effects of CA-12 stromal cells, we found that these cells provided some soluble factors that suppressed CS-21 cell apoptosis. We recently found that cysteine was an antiapoptotic soluble factor. In this report, we identify interleukin-7 (IL-7) as another antiapoptotic soluble factor secreted by CA-12 stromal cells. Although the activity of CPP32-like protease was increased in induction of CS-21 cell apoptosis, the addition of IL-7 suppressed the activity. The expression of Bcl-2 protein was down-regulated when CS-21 cells were cultured alone, but the addition of IL-7 recovered the expression of Bcl-2. These results indicate that CA-12 stromal cells inhibit CS-21 cell apoptosis by producing IL-7, which leads to the suppression of CPP32-like protease activation and the expression of Bcl-2 protein.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects*
  • Caspase 1
  • Caspase 3
  • Caspases*
  • Cysteine Endopeptidases / metabolism*
  • Enzyme Activation
  • Enzyme Precursors / antagonists & inhibitors*
  • Interleukin-7 / metabolism
  • Interleukin-7 / pharmacology*
  • Lymphoma, T-Cell / metabolism
  • Lymphoma, T-Cell / pathology*
  • Mice
  • Proto-Oncogene Proteins c-bcl-2 / metabolism*
  • Stromal Cells / metabolism*

Substances

  • Enzyme Precursors
  • Interleukin-7
  • Proto-Oncogene Proteins c-bcl-2
  • Casp3 protein, mouse
  • Caspase 3
  • Caspases
  • Cysteine Endopeptidases
  • Caspase 1