Targeted deletion of CD44v7 exon leads to decreased endothelial cell injury but not tumor cell killing mediated by interleukin-2-activated cytolytic lymphocytes

J Biol Chem. 2003 Oct 31;278(44):43818-30. doi: 10.1074/jbc.M304467200. Epub 2003 Aug 6.

Abstract

In the current study, we investigated the nature and role of CD44 variant isoforms involved in endothelial cell (EC) injury and tumor cell cytotoxicity mediated by IL-2-activated killer (LAK) cells. Treatment of CD44 wild-type lymphocytes with IL-2 led to increased gene expression of CD44 v6 and v7 variant isoforms and to significant induction of vascular leak syndrome (VLS). CD44v6-v7 knockout (KO) and CD44v7 KO mice showed markedly reduced levels of IL-2-induced VLS. The decreased VLS in CD44v6-v7 KO and CD44v7 KO mice did not result from differential activation and expansion of CD8+ T cells, NK, and NK-T cells or from altered degree of perivascular lymphocytic infiltration in the lungs. LAK cells from CD44v7 KO mice showed a significant decrease in their ability to adhere to and mediate lysis of EC but not lysis of P815 tumor cells in vitro. CD44v7-mediated lysis of EC by LAK cells was dependent on the activity of phosphatidylinositol 3-kinase and tyrosine kinases. Interestingly, IL-2-activated LAK cells expressing CD44hi but not CD44lo were responsible for EC lysis. Furthermore, lysis of EC targets could be blocked by addition of soluble or enzymatic cleavage of CD44v6-v7-binding glycosaminoglycans. Finally, anti-CD44v7 mAbs caused a significant reduction in the adherence to and killing of EC and led to suppression of IL-2-induced VLS. Together, this study suggests that the expression of CD44v7 on LAK cells plays a specific role in EC injury and that it may be possible to reduce EC injury but not tumor cell killing by specifically targeting CD44v7.

Publication types

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

MeSH terms

  • Animals
  • Cell Adhesion
  • Cell Membrane / metabolism
  • Cloning, Molecular
  • Endothelial Cells / pathology
  • Endothelium, Vascular / pathology
  • Enzyme Activation
  • Exons*
  • Female
  • Flow Cytometry
  • Glycoproteins / biosynthesis
  • Hyaluronan Receptors / biosynthesis
  • Hyaluronan Receptors / genetics*
  • Interleukin-2 / metabolism
  • Killer Cells, Lymphokine-Activated / metabolism*
  • Ligands
  • Lung / immunology
  • Lymphocytes / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mitogens / metabolism
  • Mutagenesis, Site-Directed
  • Phosphatidylinositol 3-Kinases / metabolism
  • Protein Binding
  • Protein Isoforms
  • RNA / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Spleen / pathology
  • Up-Regulation

Substances

  • CD44v6 antigen
  • Cd44 protein, mouse
  • Glycoproteins
  • Hyaluronan Receptors
  • Interleukin-2
  • Ligands
  • Mitogens
  • Protein Isoforms
  • RNA
  • Phosphatidylinositol 3-Kinases