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

被引:214
作者
Delacour, D
Gouyer, V
Zanetta, JP
Drobecq, H
Leteurtre, E
Grard, G
Moreau-Hannedouche, O
Maes, E
Pons, A
André, S
Le Bivic, A
Gabius, HJ
Manninen, A
Simons, K
Huet, G [1 ]
机构
[1] INSERM, Unite 560, F-59045 Lille, France
[2] CNRS, UMR 8576, Unite Glycobiol Struct & Fonct, F-59655 Villeneuve Dascq, France
[3] CNRS, Inst Biol, UMR 8525, F-59021 Lille, France
[4] CNRS, Inst Pasteur Lille, UMR 8525, F-59021 Lille, France
[5] Hop Claude Huriez, Biochim Lab, F-59045 Lille, France
[6] Univ Munich, Fac Vet Med, Inst Physiol Chem, D-80539 Munich, Germany
[7] Fac Sci Luminy, Lab NMDA, IBDM, F-13288 Marseille, France
[8] Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany
关键词
D O I
10.1083/jcb.200407073
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We have previously reported that 1-benzyl-2-acetamido-2-deoxy-alpha-D-galactopyranoside-(GalNac alpha-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 W 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.
引用
收藏
页码:491 / 501
页数:11
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