PTEN regulates motility but not directionality during leukocyte chemotaxis

J Cell Sci. 2004 Dec 1;117(Pt 25):6207-15. doi: 10.1242/jcs.01545.

Abstract

The localization at opposite cell poles of phosphatidylinositol-3 kinases and PTEN (phosphatase and tensin homolog on chromosome 10) governs Dictyostelium chemotaxis. To study this model in mammalian cells, we analyzed the dynamic redistribution of green fluorescent protein (GFP)-tagged PTEN chimeras during chemotaxis. N- or C-terminus GFP-tagged PTEN was distributed homogeneously in the cytoplasm of chemotaxing PTEN-negative Jurkat cells and PTEN-positive HL60 cells. Moreover, we did not detect uropod accumulation of endogenous PTEN in chemoattractant-stimulated HL60 cells. Cell fractionation indicated that both endogenous and ectopically expressed PTEN were confined largely to the cytosol, and that chemoattractant stimulation did not alter this location. PTEN re-expression in Jurkat cells or PTEN depletion by specific siRNA in HL60 cells did not affect cell gradient sensing; PTEN nonetheless modulated chemoattractant-induced actin polymerization and the speed of cell movement. The results suggest a role for PTEN in regulating actin polymerization, but not directionality during mammalian cell chemotaxis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / metabolism
  • Blotting, Western
  • Catalysis
  • Cell Movement
  • Chemotactic Factors / pharmacology
  • Chemotaxis
  • Cloning, Molecular
  • Cytoplasm / metabolism
  • Cytosol / metabolism
  • DNA, Complementary / metabolism
  • Dose-Response Relationship, Drug
  • Green Fluorescent Proteins / metabolism
  • HL-60 Cells
  • Humans
  • Jurkat Cells
  • Leukocytes / cytology*
  • Membrane Microdomains / metabolism
  • Microscopy, Fluorescence
  • Microscopy, Video
  • PTEN Phosphohydrolase
  • Phosphatidylinositol 3-Kinases / metabolism
  • Phosphoric Monoester Hydrolases / metabolism
  • Phosphoric Monoester Hydrolases / physiology*
  • Protein Structure, Tertiary
  • RNA, Small Interfering / metabolism
  • Subcellular Fractions / metabolism
  • Time Factors
  • Tumor Suppressor Proteins / metabolism
  • Tumor Suppressor Proteins / physiology*

Substances

  • Actins
  • Chemotactic Factors
  • DNA, Complementary
  • RNA, Small Interfering
  • Tumor Suppressor Proteins
  • Green Fluorescent Proteins
  • Phosphatidylinositol 3-Kinases
  • Phosphoric Monoester Hydrolases
  • PTEN Phosphohydrolase
  • PTEN protein, human