Protein phosphatase 2A in stretch-induced endothelial cell proliferation

J Cell Biochem. 1996 Dec 1;63(3):311-9. doi: 10.1002/(SICI)1097-4644(19961201)63:3%3C311::AID-JCB6%3E3.0.CO;2-#.

Abstract

We previously proposed that activation of protein kinase C is a key mechanism for control of cell growth enhanced by cyclic strain [Rosales and Sumpio (1992): Surgery 112:459-466]. Here we examined protein phosphatase 1 and 2A activity in bovine aortic endothelial cells exposed to cyclic stain. Protein phosphatase 2A activity in the cytosol was decreased by 36.1% in response to cyclic strain for 60 min, whereas the activity in the membrane did not change. Treatment with low concentration (0.1 nM) of okadaic acid enhanced proliferation of both static and stretched endothelial cells in 10% fetal bovine serum. These data suggest that protein phosphatase 2A acts as a growth suppressor and cyclic strain may enhance cellular proliferation by inhibiting protein phosphatase 2A as well as stimulating protein kinase C.

MeSH terms

  • Animals
  • Cattle
  • Cell Division
  • Cells, Cultured
  • Endothelium, Vascular / enzymology*
  • Endothelium, Vascular / pathology
  • Phosphoprotein Phosphatases / analysis*
  • Protein Phosphatase 1
  • Protein Phosphatase 2
  • Stress, Mechanical

Substances

  • Phosphoprotein Phosphatases
  • Protein Phosphatase 1
  • Protein Phosphatase 2