Roles of cortactin, an actin polymerization mediator, in cell endocytosis

Acta Biochim Biophys Sin (Shanghai). 2006 Feb;38(2):95-103. doi: 10.1111/j.1745-7270.2006.00141.x.

Abstract

Cortactin, an actin-binding protein and a substrate of Src, is encoded by the EMS1 oncogene. Cortactin is known to activate Arp2/3 complex-mediated actin polymerization and interact with dynamin, a large GTPase and proline rich domain-containing protein. Transferrin endocytosis was significantly reduced in cells by knock-down of cortactin expression as well as in vivo introduction of cortactin immunoreagents. Cortactin-dynamin interaction displayed morphologically dynamic co-distribution with a change in the endocytosis level in cells treated with an actin depolymerization reagent, cytochalasin D. In an in vitro beads assay, a branched actin network was recruited onto dynamin-coated beads in a cortactin Src homology domain 3 (SH3)-dependent manner. In addition, cortactin was found to function in the late stage of clathrin coated vesicle formation. Taken together, cortactin is required for optimal clathrin mediated endocytosis in a dynamin directed manner.

MeSH terms

  • Actin-Related Protein 2 / chemistry
  • Actin-Related Protein 2 / metabolism
  • Actin-Related Protein 3 / chemistry
  • Actin-Related Protein 3 / metabolism
  • Actins / chemistry
  • Actins / metabolism*
  • Animals
  • Blotting, Western
  • Cell Membrane / metabolism
  • Clathrin-Coated Vesicles / metabolism
  • Codon / genetics
  • Cortactin / chemistry
  • Cortactin / metabolism*
  • Cytochalasin D / pharmacology
  • Endocytosis / physiology*
  • GTP Phosphohydrolases / metabolism
  • Humans
  • Microfilament Proteins / chemistry
  • Microfilament Proteins / metabolism*
  • Microscopy, Fluorescence
  • Oncogene Proteins / genetics
  • Polymers / chemistry
  • Polymers / metabolism
  • Transferrin / metabolism
  • src Homology Domains

Substances

  • Actin-Related Protein 2
  • Actin-Related Protein 3
  • Actins
  • Codon
  • Cortactin
  • Microfilament Proteins
  • Oncogene Proteins
  • Polymers
  • Transferrin
  • Cytochalasin D
  • GTP Phosphohydrolases