Integrity of the cortical actin ring is required for activation of the PI3K/Akt and p38 MAPK signaling pathways in redifferentiation of chondrocytes on chitosan

Cell Biol Int. 2008 Oct;32(10):1272-8. doi: 10.1016/j.cellbi.2008.07.013. Epub 2008 Jul 25.

Abstract

Cell shape alterations and accompanying cytoskeletal changes have diverse effects on cell function. We have already shown that dedifferentiated chondrocytes have a round cell morphology and undergo redifferentiation when cultured on chitosan membrane. In the present study, we investigate the role of the cytoskeleton in chondrocyte redifferentiation. Chondrocytes obtained from a micromass culture of chick limb bud mesenchymal cells were subcultured four times. Immunofluorescence analysis of F-actin showed cortical distribution of the actin cytoskeleton upon subculture of dedifferentiated chondrocytes on chitosan membrane. Treatment with cytochalasin D disrupted the cortical actin ring formed during cultivation of chondrocytes on the chitosan membrane, and inhibited chondrocyte redifferentiation. Moreover, cytochalasin D inhibited the phosphorylation of Akt and p38 mitogen activated protein kinase (MAPK), induced during redifferentiation on chitosan membrane. LY294002, an inhibitor of phosphatidylinositol-3-OH-kinase (PI3K), suppressed chondrocyte redifferentiation. These findings suggest that integrity of the actin cytoskeleton is a crucial requirement for PI3K/Akt and p38 MAPK in chondrocyte redifferentiation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / metabolism
  • Animals
  • Cell Differentiation / physiology*
  • Cell Shape
  • Cells, Cultured
  • Chick Embryo
  • Chitosan / metabolism*
  • Chondrocytes* / cytology
  • Chondrocytes* / physiology
  • Cytochalasin D / metabolism
  • Cytoskeleton / metabolism*
  • Enzyme Activation
  • Enzyme Inhibitors / metabolism
  • MAP Kinase Signaling System / physiology*
  • Nucleic Acid Synthesis Inhibitors / metabolism
  • Phosphatidylinositol 3-Kinases / metabolism*
  • Proto-Oncogene Proteins c-akt / metabolism*
  • p38 Mitogen-Activated Protein Kinases / metabolism*

Substances

  • Actins
  • Enzyme Inhibitors
  • Nucleic Acid Synthesis Inhibitors
  • Cytochalasin D
  • Chitosan
  • Phosphatidylinositol 3-Kinases
  • Proto-Oncogene Proteins c-akt
  • p38 Mitogen-Activated Protein Kinases