Inhibition of cell movement and proliferation by cell-cell contact-induced interaction of Necl-5 with nectin-3

J Cell Biol. 2005 Oct 10;171(1):165-73. doi: 10.1083/jcb.200501090.

Abstract

Immunoglobulin-like Necl-5/Tage4/poliovirus receptor (PVR)/CD155, originally identified as the PVR, has been shown to be up-regulated in cancer cells and to enhance growth factor-induced cell movement and proliferation. In addition, Necl-5 heterophilically trans-interacts with nectin-3, a cell-cell adhesion molecule known to form adherens junctions in cooperation with cadherin. We show here that Necl-5 was down-regulated from cell surface upon cell-cell contacts in NIH3T3 cells. This down-regulation of Necl-5 was initiated by its interaction with nectin-3 and was mainly mediated by clathrin-dependent endocytosis. Then, the down-regulation of Necl-5 induced in this way reduced movement and proliferation of NIH3T3 cells. These results indicate that the down-regulation of Necl-5 induced by its interaction with nectin-3 upon cell-cell contacts may be at least one mechanism underlying contact inhibition of cell movement and proliferation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Neoplasm / genetics
  • Antigens, Neoplasm / metabolism*
  • Cell Adhesion / drug effects
  • Cell Adhesion Molecules / genetics
  • Cell Adhesion Molecules / metabolism*
  • Cell Movement / drug effects*
  • Cell Proliferation / drug effects*
  • Clathrin / metabolism
  • Down-Regulation
  • Endocytosis
  • Mice
  • NIH 3T3 Cells
  • Nectins
  • Neoplasm Proteins / genetics
  • Neoplasm Proteins / metabolism*
  • RNA, Small Interfering / genetics

Substances

  • Antigens, Neoplasm
  • Cell Adhesion Molecules
  • Clathrin
  • Nectin3 protein, mouse
  • Nectins
  • Neoplasm Proteins
  • RNA, Small Interfering
  • Taa1 protein, mouse