Galectin-4 and sulfatides in apical membrane trafficking in enterocyte-like cells

Author:

Delacour Delphine1,Gouyer Valérie1,Zanetta Jean-Pierre2,Drobecq Hervé3,Leteurtre Emmanuelle1,Grard Georges4,Moreau-Hannedouche Odile1,Maes Emmanuel2,Pons Alexandre2,André Sabine5,Le Bivic André6,Gabius Hans Joachim5,Manninen Aki7,Simons Kai7,Huet Guillemette1

Affiliation:

1. Unité INSERM 560, 59045 Lille Cedex, France

2. UMR CNRS 8576, Unité de Glycobiologie Structurale et Fonctionnelle, 59655 Villeneuve d'Ascq, France

3. UMR CNRS 8525, Institut de Biologie et Institut Pasteur de Lille, 59021 Lille, France

4. Laboratoire de Biochimie, Hôpital Claude Huriez, 59045 Lille Cedex, France

5. Institute of Physiological Chemistry, Faculty of Veterinary Medicine, Ludwig Maximilians University, D-80539 Munchen, Germany

6. Laboratoire de Neurogenese et Morphogenese au cours du Developpement et chez l'Adulte (NMDA)/Institut de Biologie du Developpement de Marseille/IBDM, Case 907, Faculté des Sciences de Luminy, 13288 Marseille Cedex 09, France

7. Max-Planck Institute of Molecular Cell Biology and Genetics, D-01307 Dresden, Germany

Abstract

We have previously reported that 1-benzyl-2-acetamido-2-deoxy-α-d-galactopyranoside (GalNAcα-O-bn), an inhibitor of glycosylation, perturbed apical biosynthetic trafficking in polarized HT-29 cells suggesting an involvement of a lectin-based mechanism. Here, we have identified galectin-4 as one of the major components of detergent-resistant membranes (DRMs) isolated from HT-29 5M12 cells. Galectin-4 was also found in post-Golgi carrier vesicles. The functional role of galectin-4 in polarized trafficking in HT-29 5M12 cells was studied by using a retrovirus-mediated RNA interference. In galectin-4–depleted HT-29 5M12 cells apical membrane markers accumulated intracellularly. In contrast, basolateral membrane markers were not affected. Moreover, galectin-4 depletion altered the DRM association characteristics of apical proteins. Sulfatides with long chain-hydroxylated fatty acids, which were also enriched in DRMs, were identified as high-affinity ligands for galectin-4. Together, our data propose that interaction between galectin-4 and sulfatides plays a functional role in the clustering of lipid rafts for apical delivery.

Publisher

Rockefeller University Press

Subject

Cell Biology

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