p120-Catenin regulates leukocyte transmigration through an effect on VE-cadherin phosphorylation

Blood. 2008 Oct 1;112(7):2770-9. doi: 10.1182/blood-2008-03-147181. Epub 2008 Jul 18.

Abstract

Vascular endothelial-cadherin (VE-cad) is localized to adherens junctions at endothelial cell borders and forms a complex with alpha-, beta-, gamma-, and p120-catenins (p120). We previously showed that the VE-cad complex disassociates to form short-lived "gaps" during leukocyte transendothelial migration (TEM); however, whether these gaps are required for leukocyte TEM is not clear. Recently p120 has been shown to control VE-cad surface expression through endocytosis. We hypothesized that p120 regulates VE-cad surface expression, which would in turn have functional consequences for leukocyte transmigration. Here we show that endothelial cells transduced with an adenovirus expressing p120GFP fusion protein significantly increase VE-cad expression. Moreover, endothelial junctions with high p120GFP expression largely prevent VE-cad gap formation and neutrophil leukocyte TEM; if TEM occurs, the length of time required is prolonged. We find no evidence that VE-cad endocytosis plays a role in VE-cad gap formation and instead show that this process is regulated by changes in VE-cad phosphorylation. In fact, a nonphosphorylatable VE-cad mutant prevented TEM. In summary, our studies provide compelling evidence that VE-cad gap formation is required for leukocyte transmigration and identify p120 as a critical intracellular mediator of this process through its regulation of VE-cad expression at junctions.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Antigens, CD / metabolism*
  • Cadherins / metabolism*
  • Catenins
  • Cell Adhesion Molecules / metabolism*
  • Cells, Cultured
  • Chemotaxis, Leukocyte*
  • Delta Catenin
  • Endocytosis
  • Endothelial Cells / cytology
  • Endothelial Cells / metabolism
  • Endothelium / metabolism
  • Gap Junctions / metabolism
  • Green Fluorescent Proteins / metabolism
  • Half-Life
  • Humans
  • Leukocytes / cytology*
  • Leukocytes / metabolism*
  • Phosphoproteins / metabolism*
  • Phosphorylation
  • Protein Binding
  • Protein Transport
  • Recombinant Fusion Proteins / metabolism

Substances

  • Antigens, CD
  • Cadherins
  • Catenins
  • Cell Adhesion Molecules
  • Phosphoproteins
  • Recombinant Fusion Proteins
  • cadherin 5
  • Green Fluorescent Proteins
  • Delta Catenin
  • CTNND1 protein, human