Purification and characterization of beta-actin-rich tumor cell pseudopodia: role of glycolysis

Exp Cell Res. 2000 Jul 10;258(1):171-83. doi: 10.1006/excr.2000.4929.

Abstract

The MSV-MDCK-INV invasive variant of Moloney sarcoma virus (mos) transformed MDCK cells express multiple beta-actin-rich pseudopodia (P. U. Le et al., Cancer Res. 58, 1631-1635, 1998). We show here that the tips of these actively protruding cellular domains are morphologically distinct presenting numerous blebs and selectively pass through 1-microm-pore filters. The pseudopodia were purified from the underside of the filters and a major protein component was identified as the glycolytic enzyme, glyceraldehyde-3-phosphate dehydrogenase (GAPDH). By confocal microscopy, GAPDH colocalized with actin in MSV-MDCK-INV pseudopodia localizing this glycolytic enzyme to this site of active actin polymerization. Inhibition of glycolysis with 2-deoxyglucose or oxamate induced a rapid transformation of beta-actin-rich pseudopodia into extended lamellipodia and prevented cell motility. A localized glycolytic supply of energy therefore regulates the formation of beta-actin-rich pseudopodial protrusions and thereby the motility of invasive tumor cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / analysis*
  • Animals
  • Cell Fractionation
  • Cell Line, Transformed
  • Cell Movement
  • Cell Transformation, Neoplastic*
  • Dogs
  • Glyceraldehyde-3-Phosphate Dehydrogenases / analysis
  • Glycolysis*
  • Kidney
  • Microscopy, Confocal
  • Microscopy, Electron, Scanning
  • Mitochondria / metabolism
  • Moloney murine sarcoma virus / physiology*
  • Oxygen Consumption
  • Pseudopodia / pathology
  • Pseudopodia / ultrastructure*

Substances

  • Actins
  • Glyceraldehyde-3-Phosphate Dehydrogenases