Source:http://linkedlifedata.com/resource/pubmed/id/17378898
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rdf:type | |
lifeskim:mentions |
umls-concept:C0006055,
umls-concept:C0026336,
umls-concept:C0035820,
umls-concept:C0226890,
umls-concept:C0282560,
umls-concept:C0439855,
umls-concept:C0449432,
umls-concept:C0449943,
umls-concept:C0872351,
umls-concept:C1179435,
umls-concept:C1518413,
umls-concept:C1524073,
umls-concept:C1548799,
umls-concept:C1705248
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pubmed:issue |
3
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pubmed:dateCreated |
2007-3-23
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pubmed:abstractText |
Botulinum neurotoxin (BoNT) is produced as a large toxin complex (TC) associated with nontoxic nonhemagglutinin (NTNHA) and three hemagglutinin subcomponents (HA-70, -33 and -17). To assess the role of nontoxic components in the oral intoxication of botulinum TCs, we investigated the permeability of serotype D strain 4947 BoNT and its various TC species through cultured Caco-2 cell monolayers. The L-TC species (complexes composed of BoNT, NTNHA, HA-70, HA-33 and HA-17) showed potent permeability through the cell layer, whereas free BoNT, M-TC (BoNT and NTNHA complexes) and M-TC/HA-70 showed little or no permeability. Cell binding tests demonstrated that HA-33/HA-17 complexes bound to cells, whereas other components did not. These findings suggest that BoNT in the 650-kDa L-TC permeates into the cell mainly in an HA-33/HA-17-mediated manner, although free BoNT can permeate into the cell. As free BoNT and M-TC were susceptible to digestion with gastrointestinal juice, it is likely that L-TC species containing HA-33 caused higher oral toxicity in mice than others. We conclude that the HA-33 subcomponent plays a critical role in the permeation of TCs into intestinal epithelium, and that other HA subcomponents protect BoNT against gastrointestinal digestion.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0928-8244
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
49
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
346-52
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:17378898-Animals,
pubmed-meshheading:17378898-Botulinum Toxins,
pubmed-meshheading:17378898-Caco-2 Cells,
pubmed-meshheading:17378898-Gastric Juice,
pubmed-meshheading:17378898-Humans,
pubmed-meshheading:17378898-Intestinal Mucosa,
pubmed-meshheading:17378898-Mice,
pubmed-meshheading:17378898-Permeability,
pubmed-meshheading:17378898-Protein Binding,
pubmed-meshheading:17378898-Protein Subunits,
pubmed-meshheading:17378898-Rats,
pubmed-meshheading:17378898-Rats, Wistar
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pubmed:year |
2007
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pubmed:articleTitle |
Role of nontoxic components of serotype D botulinum toxin complex in permeation through a Caco-2 cell monolayer, a model for intestinal epithelium.
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pubmed:affiliation |
Department of Food Science and Technology, Faculty of Bioindustry, Tokyo University of Agriculture, Abashiri, Japan. k3niwa@bioindustry.nodai.ac.jp
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pubmed:publicationType |
Journal Article
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