Regulation of the assembly and adhesion activity of E-cadherin by nectin and afadin for the formation of adherens junctions in MDCK cells

Authors:
Sato T, Fujita N, Yamada A, Ooshio T, Okamoto R, Irie K and Takai Y
In:
Source: J Biol Chem
Publication Date: (2006)
Issue: 281(8): 5288-99
Research Area:
Cancer Research/Cell Biology
Cells used in publication:
MDCK
Species: canine
Tissue Origin: kidney
Platform:
Nucleofector® I/II/2b
Abstract
The Ca2+-independent immunoglobulin-like molecule nectin first forms cell-cell adhesions and then assembles cadherin at nectin-based cell-cell adhesion sites, resulting in the formation of adherens junctions (AJs). Afadin is a nectin- and actin filament-binding protein that connects nectin to the actin cytoskeleton. Here, we studied the roles and modes of action of nectin and afadin in the formation of AJs in cultured MDCK cells. The trans-interaction of nectin assembled E-cadherin, which was associated with p120ctn, ss-catenin, and a-catenin. However, the assembled E-cadherin showed weak cell-cell adhesion activity, presumably the non-trans-interacting form, at the nectin-based cell-cell adhesion sites in an afadin-independent manner. The assembly was mediated by the IQGAP1-dependent actin cytoskeleton, which was organized by Cdc42 and Rac small G proteins that were activated by the action of trans-interacting nectin through c-Src and Rap1 small G protein in an afadin-independent manner. However, Rap1 bound to afadin, and this Rap1-afadin complex then interacted with p120ctn associated with non-trans-interacting E-cadherin, thereby causing the trans-interaction of E-cadherin. Thus, nectin regulates the assembly and cell-cell adhesion activity of E-cadherin through afadin, nectin signaling, and p120ctn for the formation of AJs in MDCK cells.