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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
52
pubmed:dateCreated
2003-12-22
pubmed:abstractText
Fibrillogenic human amylin elicits pancreatic beta-cell apoptosis that may contribute to development of type-2 diabetes. Here, we demonstrated that activation of a caspase cascade is necessary for induction of apoptosis by fibrillogenic amylin variants in two pancreatic beta-cell lines. Human amylin, as well as truncated 8-37human amylin, evoked sequential activation of caspases-8 and -3, and apoptosis, whereas non-beta-sheet forming and non-fibrillogenic homologs, such as [25,28,29triprolyl]human amylin, did not, implying that the beta-sheet conformer is required for human amylin-induced caspase activation. Significant inhibition of apoptosis was evoked by a selective caspase-1 inhibitor, indicating that caspase-1 is also essential for activation of the caspase cascade. Furthermore, we showed that specific jnk1 antisense oligonucleotides, which suppress phospho-JNK1 expression, effectively decreased human amylin-induced activation of c-Jun. Studies of the interplay between the caspase cascade and the JNK pathway showed that both apoptosis and caspase-3 activation were suppressed by treatment with a JNK inhibitor and by transfection of antisense jnk1 oligonucleotides or antisense-c-jun, whereas a selective inhibitor of caspases-1 and -3 prevented apoptosis but not c-Jun activation. Thus, the JNK1 activation preceded activation of caspases-1 and -3. However, selective JNK inhibition had no effect on caspase-8 activation, and selective caspase-8 inhibition only partially suppressed apoptosis and c-Jun activation, indicating that caspase-8 may partially act upstream of the JNK pathway. Our studies demonstrate a functional interaction of a caspase cascade and JNK1. Fibrillogenic amylin can evoke a JNK1-mediated apoptotic pathway, which is partially dependent and partially independent of caspase-8, and in which caspase-3 acts as a common downstream effector.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Amyloid, http://linkedlifedata.com/resource/pubmed/chemical/CASP3 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/CASP8 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Casp3 protein, rat, http://linkedlifedata.com/resource/pubmed/chemical/Casp8 protein, rat, http://linkedlifedata.com/resource/pubmed/chemical/Caspase 1, http://linkedlifedata.com/resource/pubmed/chemical/Caspase 3, http://linkedlifedata.com/resource/pubmed/chemical/Caspase 8, http://linkedlifedata.com/resource/pubmed/chemical/Caspases, http://linkedlifedata.com/resource/pubmed/chemical/Enzyme Inhibitors, http://linkedlifedata.com/resource/pubmed/chemical/Fibrin, http://linkedlifedata.com/resource/pubmed/chemical/Islet Amyloid Polypeptide, http://linkedlifedata.com/resource/pubmed/chemical/Mitogen-Activated Protein Kinase 8, http://linkedlifedata.com/resource/pubmed/chemical/Mitogen-Activated Protein Kinases, http://linkedlifedata.com/resource/pubmed/chemical/Peptides
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0021-9258
pubmed:author
pubmed:issnType
Print
pubmed:day
26
pubmed:volume
278
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
52810-9
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:14532296-Amyloid, pubmed-meshheading:14532296-Animals, pubmed-meshheading:14532296-Apoptosis, pubmed-meshheading:14532296-Blotting, Western, pubmed-meshheading:14532296-Caspase 1, pubmed-meshheading:14532296-Caspase 3, pubmed-meshheading:14532296-Caspase 8, pubmed-meshheading:14532296-Caspases, pubmed-meshheading:14532296-Cell Line, Tumor, pubmed-meshheading:14532296-Enzyme Activation, pubmed-meshheading:14532296-Enzyme Inhibitors, pubmed-meshheading:14532296-Enzyme-Linked Immunosorbent Assay, pubmed-meshheading:14532296-Fibrin, pubmed-meshheading:14532296-Humans, pubmed-meshheading:14532296-Immunohistochemistry, pubmed-meshheading:14532296-Insulinoma, pubmed-meshheading:14532296-Islet Amyloid Polypeptide, pubmed-meshheading:14532296-Islets of Langerhans, pubmed-meshheading:14532296-Mitogen-Activated Protein Kinase 8, pubmed-meshheading:14532296-Mitogen-Activated Protein Kinases, pubmed-meshheading:14532296-Peptides, pubmed-meshheading:14532296-Protein Structure, Secondary, pubmed-meshheading:14532296-Protein Structure, Tertiary, pubmed-meshheading:14532296-Rats, pubmed-meshheading:14532296-Time Factors
pubmed:year
2003
pubmed:articleTitle
Fibrillogenic amylin evokes islet beta-cell apoptosis through linked activation of a caspase cascade and JNK1.
pubmed:affiliation
School of Biological Sciences, Faculty of Science, University of Auckland, 3 Symonds St., Level 4.1, Private Bag 92019, Auckland, New Zealand.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't