Source:http://linkedlifedata.com/resource/pubmed/id/18849568
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
50
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pubmed:dateCreated |
2008-12-8
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pubmed:abstractText |
Sulfated glycans play critical roles in various cell recognition events among leukocytes. The 6-sulfated lactosamine glycans in particular have been widely noted for their importance because they are involved in cell recognition events mediated by cell-adhesion molecules such as selectins and sialic acid-recognizing molecules such as siglecs and also in the activation of CD44 in binding to extracellular matrix hyaluronate. A pro-inflammatory cytokine, tumor necrosis factor-alpha, induces expression of 6-sulfated glycans on human leukocytes. Here we report that the transcription of the GlcNAc6ST-1 gene, the gene encoding a sulfotransferase for 6-sulfated glycan synthesis, is induced in human T-lymphoid cells through tandem NF-kappaB and GATA motifs in its 5'-regulatory region. Results of our reporter assays, immunoprecipitation, and chromatin immunoprecipitation analyses indicated that GATA-3 and/or GATA-2, but not GATA-1, associates with NF-kappaB in a transcription factor complex on the 5'-regulatory region of the gene and acts synergistically with NF-kappaB in triggering GlcNAc6ST-1 transcription. Recently, a skin-homing subset of helper memory T cells exhibiting the Th2 marker CCR4 was shown to specifically express 6-sulfated glycans. The transactivation mechanism described here suggested that GlcNAc6ST-1 transcription is coordinated with the NF-kappaB/GATA-3 axis, which is known to figure heavily in Th2 cell differentiation. In line with this, in vitro differentiation of human T cells to Th2 cells was found to significantly induce GlcNAc6ST-1 transcription and 6-sulfated glycan expression.
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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, CD44,
http://linkedlifedata.com/resource/pubmed/chemical/CCR4 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/GATA2 Transcription Factor,
http://linkedlifedata.com/resource/pubmed/chemical/GATA2 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/GATA3 Transcription Factor,
http://linkedlifedata.com/resource/pubmed/chemical/GATA3 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Hyaluronic Acid,
http://linkedlifedata.com/resource/pubmed/chemical/NF-kappa B,
http://linkedlifedata.com/resource/pubmed/chemical/Polysaccharides,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, CCR4,
http://linkedlifedata.com/resource/pubmed/chemical/Sulfotransferases,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Necrosis Factor-alpha,
http://linkedlifedata.com/resource/pubmed/chemical/carbohydrate sulfotransferases
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0021-9258
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
12
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pubmed:volume |
283
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
34563-70
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pubmed:meshHeading |
pubmed-meshheading:18849568-Antigens, CD44,
pubmed-meshheading:18849568-Base Sequence,
pubmed-meshheading:18849568-Cell Differentiation,
pubmed-meshheading:18849568-GATA2 Transcription Factor,
pubmed-meshheading:18849568-GATA3 Transcription Factor,
pubmed-meshheading:18849568-Humans,
pubmed-meshheading:18849568-Hyaluronic Acid,
pubmed-meshheading:18849568-Jurkat Cells,
pubmed-meshheading:18849568-Molecular Sequence Data,
pubmed-meshheading:18849568-NF-kappa B,
pubmed-meshheading:18849568-Polysaccharides,
pubmed-meshheading:18849568-Receptors, CCR4,
pubmed-meshheading:18849568-Sulfotransferases,
pubmed-meshheading:18849568-T-Lymphocytes,
pubmed-meshheading:18849568-Th2 Cells,
pubmed-meshheading:18849568-Transcription, Genetic,
pubmed-meshheading:18849568-Tumor Necrosis Factor-alpha
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pubmed:year |
2008
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pubmed:articleTitle |
Significance of NF-kappaB/GATA axis in tumor necrosis factor-alpha-induced expression of 6-sulfated cell recognition glycans in human T-lymphocytes.
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pubmed:affiliation |
Department of Molecular Pathology, Aichi Cancer Center, Nagoya 464-8681, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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