A novel type of adhering junction in an epithelioid tumorigenic rat cell culture line

Cell Tissue Res. 1998 Oct;294(1):11-25. doi: 10.1007/s004410051152.

Abstract

Two major types of plaque-bearing adhering junctions are commonly distinguished: the actin microfilament-anchoring adhaerens junctions (AJs) and the desmosomes anchoring intermediate-sized filaments (IFs). Both types of junction usually possess the common plaque protein, plakoglobin, whereas the other plaque proteins and the transmembrane cadherins are mutually exclusive. For example, AJs contain E-, N-, or P-cadherin in combination with alpha- and beta-catenin, vinculin and alpha-actinin, whereas in desmosomes, desmogleins and desmocollins are associated with desmoplakin and one or several of the plakophilins (PP1-3). Here we describe a novel type of adhering junction comprising proteins of both AJs and desmosomes and the tight junction (TJ) plaque protein, ZO-1, in a newly established, liver-derived tumorigenic rat cell line (RMEC-1). By immunofluorescence microscopy, cell-cell contacts are characterized by mostly continuous-appearing lines which are usually resolved by electron microscopy as extended arrays of closely spaced small plaque subunits. These plaque-covered regions are positive for plakoglobin, alpha- and beta-catenin, the arm-repeat protein p120, vinculin, desmoplakin and protein ZO-1. They are positive for E-cadherin in cultures early on in passaging, but tend to turn negative for all known cadherins in densely grown cultures. On immunoblotting SDS-PAGE-separated proteins from dense-grown cell monolayers, "pan-cadherin" antibodies have reacted with a band at approximately 140 kDa, identified as N-cadherin by peptide fingerprinting of the immunoprecipitated protein, which for reasons not yet clear is modified or masked in immunolocalization experiments. The exact histological derivation of RMEC-1 cells is not known. However, the observations of several endothelial markers and the fact that all cells are rich in IFs containing vimentin and/or desmin, while only subpopulations also reveal IFs containing CKs 8 and 18, is suggestive of a mesenchymal, probably endothelial origin. We discuss the molecular relationship of this novel type of extended junction with other types of adhering junctions.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Cadherins / metabolism
  • Cell Adhesion Molecules / metabolism
  • Cytoskeletal Proteins / metabolism
  • Desmocollins
  • Desmogleins
  • Desmoplakins
  • Desmosomes / metabolism
  • Desmosomes / ultrastructure
  • Intercellular Junctions / metabolism*
  • Intercellular Junctions / ultrastructure*
  • Membrane Proteins / metabolism
  • Mice
  • Mice, Nude
  • Microscopy, Electron
  • Microscopy, Fluorescence
  • Neoplasms, Experimental / metabolism
  • Neoplasms, Experimental / pathology
  • Phosphoproteins / metabolism
  • Rats
  • Trans-Activators*
  • Tumor Cells, Cultured
  • Vinculin / metabolism
  • Zonula Occludens-1 Protein
  • alpha Catenin
  • beta Catenin
  • gamma Catenin

Substances

  • CTNNB1 protein, mouse
  • Cadherins
  • Cell Adhesion Molecules
  • Ctnna1 protein, mouse
  • Ctnnb1 protein, rat
  • Cytoskeletal Proteins
  • Desmocollins
  • Desmogleins
  • Desmoplakins
  • Dsp protein, mouse
  • Membrane Proteins
  • Phosphoproteins
  • Tjp1 protein, mouse
  • Tjp1 protein, rat
  • Trans-Activators
  • Zonula Occludens-1 Protein
  • alpha Catenin
  • beta Catenin
  • gamma Catenin
  • Vinculin