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

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 t...

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Autores principales: Delacour, Delphine, Gouyer, Valérie, Zanetta, Jean-Pierre, Drobecq, Hervé, Leteurtre, Emmanuelle, Grard, Georges, Moreau-Hannedouche, Odile, Maes, Emmanuel, Pons, Alexandre, André, Sabine, Le Bivic, André, Gabius, Hans Joachim, Manninen, Aki, Simons, Kai, Huet, Guillemette
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2171948/
https://www.ncbi.nlm.nih.gov/pubmed/15883199
http://dx.doi.org/10.1083/jcb.200407073
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author Delacour, Delphine
Gouyer, Valérie
Zanetta, Jean-Pierre
Drobecq, Hervé
Leteurtre, Emmanuelle
Grard, Georges
Moreau-Hannedouche, Odile
Maes, Emmanuel
Pons, Alexandre
André, Sabine
Le Bivic, André
Gabius, Hans Joachim
Manninen, Aki
Simons, Kai
Huet, Guillemette
author_facet Delacour, Delphine
Gouyer, Valérie
Zanetta, Jean-Pierre
Drobecq, Hervé
Leteurtre, Emmanuelle
Grard, Georges
Moreau-Hannedouche, Odile
Maes, Emmanuel
Pons, Alexandre
André, Sabine
Le Bivic, André
Gabius, Hans Joachim
Manninen, Aki
Simons, Kai
Huet, Guillemette
author_sort Delacour, Delphine
collection PubMed
description 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.
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spelling pubmed-21719482008-03-05 Galectin-4 and sulfatides in apical membrane trafficking in enterocyte-like cells Delacour, Delphine Gouyer, Valérie Zanetta, Jean-Pierre Drobecq, Hervé Leteurtre, Emmanuelle Grard, Georges Moreau-Hannedouche, Odile Maes, Emmanuel Pons, Alexandre André, Sabine Le Bivic, André Gabius, Hans Joachim Manninen, Aki Simons, Kai Huet, Guillemette J Cell Biol Research Articles 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. The Rockefeller University Press 2005-05-09 /pmc/articles/PMC2171948/ /pubmed/15883199 http://dx.doi.org/10.1083/jcb.200407073 Text en Copyright © 2005, The Rockefeller University Press https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/ (https://creativecommons.org/licenses/by-nc-sa/4.0/) ).
spellingShingle Research Articles
Delacour, Delphine
Gouyer, Valérie
Zanetta, Jean-Pierre
Drobecq, Hervé
Leteurtre, Emmanuelle
Grard, Georges
Moreau-Hannedouche, Odile
Maes, Emmanuel
Pons, Alexandre
André, Sabine
Le Bivic, André
Gabius, Hans Joachim
Manninen, Aki
Simons, Kai
Huet, Guillemette
Galectin-4 and sulfatides in apical membrane trafficking in enterocyte-like cells
title Galectin-4 and sulfatides in apical membrane trafficking in enterocyte-like cells
title_full Galectin-4 and sulfatides in apical membrane trafficking in enterocyte-like cells
title_fullStr Galectin-4 and sulfatides in apical membrane trafficking in enterocyte-like cells
title_full_unstemmed Galectin-4 and sulfatides in apical membrane trafficking in enterocyte-like cells
title_short Galectin-4 and sulfatides in apical membrane trafficking in enterocyte-like cells
title_sort galectin-4 and sulfatides in apical membrane trafficking in enterocyte-like cells
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2171948/
https://www.ncbi.nlm.nih.gov/pubmed/15883199
http://dx.doi.org/10.1083/jcb.200407073
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