Identification of focal adhesion kinase (FAK) and phosphatidylinositol 3-kinase (PI3-kinase) as Par3 partners by proteomic analysis

Cytoskeleton (Hoboken). 2010 May;67(5):297-308. doi: 10.1002/cm.20444.

Abstract

Partition defective 3 (Par3) is involved in a variety of polarity events including establishment of apico-basal polarity of epithelial cell, axon/dendrite specification of neurons and directional migration of cells with front-rear polarity. Par3 is thought to regulate cell polarity as a scaffold protein by interacting with various partner proteins such as Par6, aPKC, Tiam1/2 and Numb. However, the mode of actions of Par3 in polarized migration remains largely unknown. To explore Par3 functions, we screened Par3-interacting proteins by combining Par3 affinity column chromatography and shotgun analysis using liquid chromatography-tandem mass spectrometry (LC-MS/MS). We obtained about two hundred Par3-interacting proteins from the rat brain cytosol fraction. Among them, we focused on FAK and PI3-kinase, as both of them participate in directional cell migration. FAK associated with the PDZ domain and the coiled-coil region of Par3 and p110 of PI3-kinase associated with the coiled-coil region of Par3. Par3 was partially colocalized with FAK in spreading cells. Depletion of Par3 by RNA interference inhibited adhesion-induced activation of FAK and PI3-kinase, and RNA interference-resistant Par3 restored the inhibitory effects. In addition, Par3 was required for the adhesion-induced cell spreading as well as for directional cell migration toward collagen. These results suggest that Par3 directly interacts with FAK and PI3-kinase, enhancing their activities for polarized cell migration.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing
  • Animals
  • COS Cells
  • Cell Cycle Proteins / metabolism*
  • Cell Movement
  • Cell Polarity / physiology
  • Chlorocebus aethiops
  • Chromatography, Affinity
  • Chromatography, Liquid
  • Focal Adhesion Protein-Tyrosine Kinases / metabolism*
  • HeLa Cells
  • Humans
  • Membrane Proteins / metabolism*
  • Phosphatidylinositol 3-Kinases / metabolism*
  • Proteomics*
  • Tandem Mass Spectrometry

Substances

  • Adaptor Proteins, Signal Transducing
  • Cell Cycle Proteins
  • Membrane Proteins
  • PARD3 protein, human
  • Focal Adhesion Protein-Tyrosine Kinases