Source:http://linkedlifedata.com/resource/pubmed/id/19203796
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7
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pubmed:dateCreated |
2009-3-25
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pubmed:abstractText |
Since transmembrane tumor necrosis factor-alpha (tmTNF-alpha) has been reported to have a palmitoylated site at Cys(-47), and therefore its functions may be linked to lipid raft membrane microdomains. The present study tested a hypothesis that lipid rafts may serve as a signaling platform to mediate the bioactivity of tmTNF-alpha. We found that destruction of lipid rafts with methyl-beta-cyclodextrin (MCD) in Raji cells almost completely blocked the cytotoxicity of tmTNF-alpha, as did an anti-TNF-alpha antibody. Although a proportion of tmTNF-alpha was colocated with lipid rafts, either the replacement of Cys at -47 by Ala, destructing its possible lipid rafts-attaching site or the displacement of its cytoplasmic domain by the C-terminal sequence (131-157) of caveolin-1, making all tmTNF-alpha target to lipid rafts, had no effect on tmTNF-alpha cytotoxicity. The data suggest that the cytotoxicity of tmTNF-alpha is not associated with its lipid rafts location. Unparallel to decreased cytotoxicity, moreover, MCD significantly increased tmTNF-alpha expression on the cell surface, and these increased tmTNF-alpha molecules were capable of binding to sTNFR1. To further explore the mechanism of lipid rafts-mediated cytotoxicity of tmTNF-alpha, we demonstrated that MCD led to a marked decrease in adhesion of Raji cells to T24 cells, which was due to dissociation of adhesion molecule ICAM-1 from lipid rafts. These results indicate that lipid rafts importantly participate in the cytotoxicity of tmTNF-alpha through ICAM-1 clustering and consequent enhancement of the cell-cell contact. The data suggest that lipid rafts are essential for the killing of tmTNF-alpha through the cell-cell contact mediated by ICAM-1. However, lipid rafts may limit exposure of tmTNF-alpha to the cell surface.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Surface,
http://linkedlifedata.com/resource/pubmed/chemical/Intercellular Adhesion Molecule-1,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Tumor Necrosis Factor,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Necrosis Factor-alpha
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
1872-9142
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
46
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1551-60
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pubmed:meshHeading |
pubmed-meshheading:19203796-Antigens, Surface,
pubmed-meshheading:19203796-Cell Adhesion,
pubmed-meshheading:19203796-Cell Line, Tumor,
pubmed-meshheading:19203796-Cell Membrane,
pubmed-meshheading:19203796-Cytotoxicity, Immunologic,
pubmed-meshheading:19203796-HeLa Cells,
pubmed-meshheading:19203796-Humans,
pubmed-meshheading:19203796-Immunity, Cellular,
pubmed-meshheading:19203796-Intercellular Adhesion Molecule-1,
pubmed-meshheading:19203796-Membrane Microdomains,
pubmed-meshheading:19203796-Protein Binding,
pubmed-meshheading:19203796-Protein Multimerization,
pubmed-meshheading:19203796-Protein Transport,
pubmed-meshheading:19203796-Receptors, Tumor Necrosis Factor,
pubmed-meshheading:19203796-Tumor Necrosis Factor-alpha
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pubmed:year |
2009
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pubmed:articleTitle |
Lipid rafts uncouple surface expression of transmembrane TNF-alpha from its cytotoxicity associated with ICAM-1 clustering in Raji cells.
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pubmed:affiliation |
Department of Immunology, Tongji Medical College, Huazhong University of Science and Technology, 13 Hangkong Road, Wuhan, Hubei 430030, China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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