Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
10
pubmed:dateCreated
2002-10-29
pubmed:abstractText
This study is an investigation into the mechanism of Clostridium difficile toxin A-induced apoptosis in human intestinal epithelial cells. Toxin A induced apoptosis of T84 cells in a dose- and time-dependent fashion. Toxin A-induced apoptosis was completely inhibited by blocking toxin enzymatic activity on Rho GTPases with uridine 5'-diphosphate-2',3'-dialdehyde by a nonspecific caspase inhibitor and was partially inhibited by caspase-1, -3, -6, -8, and -9 inhibitors. Caspases 3, 6, 8, and 9 and Bid activation were detected. Toxin A also induced changes in mitochondrial membrane potential and cytochrome c release at 18-24 h, a time course similar to caspase-9 activation. In conclusion, toxin A induces apoptosis by a mechanism dependent on inactivation of Rho, activation of caspases 3, 6, 8, and 9 and Bid, and mitochondrial damage followed by cytochrome c release. Toxin A proapoptotic activity may contribute to the mucosal disruption seen in toxin A-induced enteritis.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Annexin A5, http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, http://linkedlifedata.com/resource/pubmed/chemical/BH3 Interacting Domain Death..., http://linkedlifedata.com/resource/pubmed/chemical/BID protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Bacterial Toxins, http://linkedlifedata.com/resource/pubmed/chemical/CASP8 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/CASP9 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Carrier Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Caspase 8, http://linkedlifedata.com/resource/pubmed/chemical/Caspase 9, http://linkedlifedata.com/resource/pubmed/chemical/Caspases, http://linkedlifedata.com/resource/pubmed/chemical/Cytochrome c Group, http://linkedlifedata.com/resource/pubmed/chemical/Enterotoxins, http://linkedlifedata.com/resource/pubmed/chemical/Tumor Necrosis Factor-alpha, http://linkedlifedata.com/resource/pubmed/chemical/rho GTP-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/tcdA protein, Clostridium difficile
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
0022-1899
pubmed:author
pubmed:issnType
Print
pubmed:day
15
pubmed:volume
186
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1438-47
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:12404159-Annexin A5, pubmed-meshheading:12404159-Antibodies, pubmed-meshheading:12404159-Apoptosis, pubmed-meshheading:12404159-BH3 Interacting Domain Death Agonist Protein, pubmed-meshheading:12404159-Bacterial Toxins, pubmed-meshheading:12404159-Carrier Proteins, pubmed-meshheading:12404159-Caspase 8, pubmed-meshheading:12404159-Caspase 9, pubmed-meshheading:12404159-Caspases, pubmed-meshheading:12404159-Cells, Cultured, pubmed-meshheading:12404159-Cytochrome c Group, pubmed-meshheading:12404159-DNA Fragmentation, pubmed-meshheading:12404159-Dose-Response Relationship, Drug, pubmed-meshheading:12404159-Drug Interactions, pubmed-meshheading:12404159-Enterotoxins, pubmed-meshheading:12404159-Humans, pubmed-meshheading:12404159-Membrane Potentials, pubmed-meshheading:12404159-Mitochondria, pubmed-meshheading:12404159-Time Factors, pubmed-meshheading:12404159-Tumor Necrosis Factor-alpha, pubmed-meshheading:12404159-rho GTP-Binding Proteins
pubmed:year
2002
pubmed:articleTitle
Mechanism of Clostridium difficile toxin A-induced apoptosis in T84 cells.
pubmed:affiliation
Department of Morphology, Federal University of Ceará, Fortaleza, Brazil.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't