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Galectin-3 regulates desmoglein-2 and intestinal epithelial intercellular adhesion.

Authors :
Jiang K
Rankin CR
Nava P
Sumagin R
Kamekura R
Stowell SR
Feng M
Parkos CA
Nusrat A
Source :
The Journal of biological chemistry [J Biol Chem] 2014 Apr 11; Vol. 289 (15), pp. 10510-10517. Date of Electronic Publication: 2014 Feb 24.
Publication Year :
2014

Abstract

The desmosomal cadherins, desmogleins, and desmocollins mediate strong intercellular adhesion. Human intestinal epithelial cells express the desmoglein-2 isoform. A proteomic screen for Dsg2-associated proteins in intestinal epithelial cells identified a lectin referred to as galectin-3 (Gal3). Gal3 bound to N-linked β-galactosides in Dsg2 extracellular domain and co-sedimented with caveolin-1 in lipid rafts. Down-regulation of Gal3 protein or incubation with lactose, a galactose-containing disaccharide that competitively inhibits galectin binding to Dsg2, decreased intercellular adhesion in intestinal epithelial cells. In the absence of functional Gal3, Dsg2 protein was internalized from the plasma membrane and degraded in the proteasome. These results report a novel role of Gal3 in stabilizing a desmosomal cadherin and intercellular adhesion in intestinal epithelial cells.

Details

Language :
English
ISSN :
1083-351X
Volume :
289
Issue :
15
Database :
MEDLINE
Journal :
The Journal of biological chemistry
Publication Type :
Academic Journal
Accession number :
24567334
Full Text :
https://doi.org/10.1074/jbc.M113.538538