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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...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2005
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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. |
format | Text |
id | pubmed-2171948 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
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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