The Kit-activating mutation D816V enhances stem cell factor--dependent chemotaxis

Blood. 2001 Aug 15;98(4):1195-9. doi: 10.1182/blood.v98.4.1195.

Abstract

The D816V mutation of c-kit has been detected in patients with mastocytosis. This mutation leads to constitutive tyrosine kinase activation of Kit. Because stem cell factor (SCF), the ligand for Kit (CD117(+)), is a chemoattractant for CD117(+) cells and one feature of mastocytosis is an abnormal collection of mast cells in tissues derived from CD34(+)CD117(+) mast cell precursors, the hypothesis was considered that the D816V mutation would enhance chemotaxis of these precursor cells. Constructs encoding wild-type Kit or Kit bearing the D816V mutation were transfected into Jurkat cells, labeled with Calcein-AM, and migration to SCF assessed in the presence or absence of tyrosine kinase inhibitors. Chemotaxis to SCF was enhanced in D816V transfectants compared to wild-type Kit transfectants (P <.002). Migration of both transfectants was inhibited by tyrosine kinase inhibitors, although D816V transfectants were more sensitive. Chemotaxis was next performed on CD34(+)CD117(+) circulating mast cell precursors obtained from patients with mastocytosis. Analysis of prechemotaxis and migrated cells showed that whereas less than 10% in the prechemotaxis sample had the D816V mutation, 40% to 80% of migrated cells had this mutation. These results demonstrate that the D816V Kit mutation enhances chemotaxis of CD117(+) cells, offering one explanation for increased mast cells observed in tissues of patients with mastocytosis. (Blood. 2001;98:1195-1199)

Publication types

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

MeSH terms

  • Antigens, CD34
  • Chemotaxis / drug effects*
  • Chemotaxis / genetics
  • Drug Synergism
  • Enzyme Inhibitors / pharmacology
  • Humans
  • Jurkat Cells
  • Mastocytosis / etiology*
  • Mastocytosis / genetics
  • Mastocytosis / pathology
  • Mutation, Missense*
  • Protein-Tyrosine Kinases / antagonists & inhibitors
  • Proto-Oncogene Proteins c-kit / genetics*
  • Proto-Oncogene Proteins c-kit / metabolism
  • Stem Cell Factor / pharmacology*
  • Transfection
  • Tumor Cells, Cultured

Substances

  • Antigens, CD34
  • Enzyme Inhibitors
  • Stem Cell Factor
  • Protein-Tyrosine Kinases
  • Proto-Oncogene Proteins c-kit