Literature DB >> 18041581

Involvement of very long fatty acid-containing lactosylceramide in lactosylceramide-mediated superoxide generation and migration in neutrophils.

Kazuhisa Iwabuchi1, Alessandro Prinetti, Sandro Sonnino, Laura Mauri, Toshihide Kobayashi, Kumiko Ishii, Naoko Kaga, Kimie Murayama, Hidetake Kurihara, Hitoshi Nakayama, Fumiko Yoshizaki, Kenji Takamori, Hideoki Ogawa, Isao Nagaoka.   

Abstract

The neutral glycosphingolipid lactosylceramide (LacCer) forms lipid rafts (membrane microdomains) coupled with the Src family kinase Lyn on the plasma membranes of human neutrophils; ligand binding to LacCer activates Lyn, resulting in neutrophil functions, such as superoxide generation and migration (Iwabuchi and Nagaoka, Lactosylceramide-enriched glycosphingolipid signaling domain mediates superoxide generation from human neutrophils, Blood 100, 1454-1464, 2002 and Sato et al. Induction of human neutrophil chemotaxis by Candida albicans-derived beta-1,6-long glycoside side-chain-branched beta glycan, J. Leukoc. Biol. 84, 204-211, 2006). Neutrophilic differentiated HL-60 cells (D-HL-60 cells) express almost the same amount of LacCer as neutrophils. However, D-HL-60 cells do not have Lyn-associated LacCer-enriched lipid rafts and lack LacCer-mediated superoxide-generating and migrating abilities. Here, we examined the roles of LacCer molecular species of different fatty acid compositions in these processes. Liquid chromatography-mass spectrometry analyses revealed that the very long fatty acid C24:0 and C24:1 chains were the main components of LacCer (31.6% on the total fatty acid content) in the detergent-resistant membrane fraction (DRM) from neutrophil plasma membranes. In contrast, plasma membrane DRM of D-HL-60 cells included over 70% C16:0-LacCer, but only 13.6% C24-LacCer species. D-HL-60 cells loaded with C24:0 or C24:1-LacCer acquired LacCer-mediated migrating and superoxide-generating abilities, and allowed Lyn coimmunoprecipitation by anti-LacCer antibody. Lyn knockdown by siRNA completely abolished the effect of C24:1-LacCer loading on LacCer-mediated migration of D-HL-60 cells. Immunoelectron microscopy revealed that LacCer clusters were closely associated with Lyn molecules in neutrophils and C24:1-LacCer-loaded D-HL-60 cells, but not in D-HL-60 cells or C16:0-LacCer-loaded cells. Taken together, these observations suggest that LacCer species with very long fatty acids are specifically necessary for Lyn-coupled LacCer-enriched lipid raft-mediated neutrophil superoxide generation and migration.

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Year:  2007        PMID: 18041581     DOI: 10.1007/s10719-007-9084-6

Source DB:  PubMed          Journal:  Glycoconj J        ISSN: 0282-0080            Impact factor:   2.916


  56 in total

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Authors:  B Kniep; K M Skubitz
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Journal:  J Biol Chem       Date:  2002-11-04       Impact factor: 5.157

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6.  Differential effects of glycosphingolipids on the detergent-insolubility of the glycosylphosphatidylinositol-anchored membrane dipeptidase.

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10.  The location of blood group antigen A on cultured rabbit kidney cells as revealed by ferritin-labelled antibody.

Authors:  E Dimmock; D Franks; A M Glauert
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  42 in total

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Authors:  Clifford A Lingwood
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Review 5.  Secondary alterations of sphingolipid metabolism in lysosomal storage diseases.

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6.  An obligate role for membrane-associated neutral sphingomyelinase activity in orienting chemotactic migration of human neutrophils.

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7.  Individual profiles of free ceramide species and the constituent ceramide species of sphingomyelin and neutral glycosphingolipid and their alteration according to the sequential changes of environmental oxygen content in human colorectal cancer Caco-2 cells.

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8.  Lorenzo's oil inhibits ELOVL1 and lowers the level of sphingomyelin with a saturated very long-chain fatty acid.

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Journal:  J Lipid Res       Date:  2014-01-31       Impact factor: 5.922

9.  Assessing the role of glycosphingolipids in the phenotype severity of Fabry disease mouse model.

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10.  Structural characterization and dynamics of globotetraosylceramide in vascular endothelial cells under TNF-alpha stimulation.

Authors:  Tetsuya Okuda; Sin-ichi Nakakita; Ken-ichi Nakayama
Journal:  Glycoconj J       Date:  2010-02       Impact factor: 2.916

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