Rac-dependent doubling of HeLa cell area and impairment of cell migration and cell cycle by compounds from Iris germanica

Protoplasma. 2011 Oct;248(4):785-97. doi: 10.1007/s00709-010-0254-1. Epub 2011 Jan 5.

Abstract

Plants are an infinite source of bioactive compounds. We screened the Israeli flora for compounds that interfere with the organization of the actin cytoskeleton. We found an activity in lipidic extract from Iris germanica that was able to increase HeLa cell area and adhesion and augment the formation of actin stress fibers. This effect was not observed when Ref52 fibroblasts were tested and was not the result of disruption of microtubules. Further, the increase in cell area was Rac1-dependent, and the iris extract led to slight Rac activation. Inhibitor of RhoA kinase did not interfere with the ability of the iris extract to increase HeLa cell area. The increase in HeLa cell area in the presence of iris extract was accompanied by impairment of cell migration and arrest of the cell cycle at G1 although the involvement of Rac1 in these processes is not clear. Biochemical verification of the extract based on activity-mediated fractionation and nuclear magnetic resonance analysis revealed that the active compounds belong to the group of iridals, a known group of triterpenoid. Purified iripallidal was able to increase cell area of both HeLa and SW480 cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acrolein / analogs & derivatives
  • Acrolein / isolation & purification
  • Acrolein / pharmacology
  • Actin Cytoskeleton / drug effects*
  • Amides / pharmacology
  • Animals
  • Cell Adhesion
  • Cell Movement / drug effects*
  • Cell Size
  • Cyclohexanols / isolation & purification
  • Cyclohexanols / pharmacology
  • Fibroblasts / cytology
  • Fibroblasts / drug effects
  • Flow Cytometry
  • G1 Phase Cell Cycle Checkpoints
  • HeLa Cells
  • Humans
  • Iris Plant / chemistry*
  • Magnetic Resonance Spectroscopy
  • Plant Extracts / chemistry
  • Plant Extracts / pharmacology
  • Pyridines / pharmacology
  • Rats
  • Rhizome / chemistry
  • Transfection
  • Triterpenes / chemistry
  • Triterpenes / pharmacology*
  • rac1 GTP-Binding Protein / metabolism*
  • rhoA GTP-Binding Protein / metabolism

Substances

  • 26-hydroxy-22-methylcycloirid-16-enal
  • Amides
  • Cyclohexanols
  • Plant Extracts
  • Pyridines
  • RAC1 protein, human
  • Triterpenes
  • iridal
  • RHOA protein, human
  • Y 27632
  • Acrolein
  • rac1 GTP-Binding Protein
  • rhoA GTP-Binding Protein