Linked Life Data

11425895

Source:http://linkedlifedata.com/resource/pubmed/id/11425895

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
13
pubmed:dateCreated
2001-6-26
pubmed:databankReference
pubmed:abstractText
Nuclear changes, including internucleosomal DNA fragmentation, are characteristic features of neuronal apoptosis resulting from transient cerebral ischemia and related brain insults for which the molecular mechanism has not been elucidated. Recent studies suggest that a caspase-3-mediated mechanism may be involved in the process of nuclear degradation in ischemic neurons. In this study, we cloned from rat brain a homolog cDNA encoding caspase-activated deoxyribonuclease (CAD)/DNA fragmentation factor 40 (DFF40), a 40 kDa nuclear enzyme that is activated by caspase-3 and promotes apoptotic DNA degradation. Subsequently, we investigated the role of CAD/DFF40 in the induction of internucleosomal DNA fragmentation in the hippocampus in a rat model of transient global ischemia and in primary neuronal cultures under ischemia-like conditions. At 8-72 hr after ischemia, CAD/DFF40 mRNA and protein were induced in the degenerating hippocampal CA1 neurons. CAD/DFF40 formed a heterodimeric complex in the nucleus with its natural inhibitor CAD (ICAD) and was activated after ischemia in a delayed manner (>24 hr) by caspase-3, which translocated into the nucleus and cleaved ICAD. Furthermore, an induced CAD/DFF40 activity was detected in nuclear extracts in both in vivo and in vitro models, and the DNA degradation activity of CAD/DFF40 was inhibited by purified ICAD protein. These results strongly suggest that CAD/DFF40 is the endogenous endonuclease that mediates caspase-3-dependent internucleosomal DNA degradation and related nuclear alterations in ischemic neurons.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
1529-2401
pubmed:author
pubmed:issnType
Electronic
pubmed:day
1
pubmed:volume
21
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
4678-90
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:11425895-Animals, pubmed-meshheading:11425895-Apoptosis, pubmed-meshheading:11425895-Apoptosis Regulatory Proteins, pubmed-meshheading:11425895-Brain, pubmed-meshheading:11425895-Caspase 3, pubmed-meshheading:11425895-Caspases, pubmed-meshheading:11425895-Cells, Cultured, pubmed-meshheading:11425895-Cloning, Molecular, pubmed-meshheading:11425895-DNA Fragmentation, pubmed-meshheading:11425895-Deoxyribonucleases, pubmed-meshheading:11425895-Gene Expression Regulation, pubmed-meshheading:11425895-Gene Expression Regulation, Developmental, pubmed-meshheading:11425895-Hippocampus, pubmed-meshheading:11425895-Ischemic Attack, Transient, pubmed-meshheading:11425895-Male, pubmed-meshheading:11425895-Molecular Sequence Data, pubmed-meshheading:11425895-Neurons, pubmed-meshheading:11425895-Organ Specificity, pubmed-meshheading:11425895-Proteins, pubmed-meshheading:11425895-RNA, Messenger, pubmed-meshheading:11425895-Rats, pubmed-meshheading:11425895-Rats, Sprague-Dawley, pubmed-meshheading:11425895-Recombinant Fusion Proteins, pubmed-meshheading:11425895-Sequence Homology, Amino Acid
pubmed:year
2001
pubmed:articleTitle
Caspase-activated DNase/DNA fragmentation factor 40 mediates apoptotic DNA fragmentation in transient cerebral ischemia and in neuronal cultures.
pubmed:affiliation
Department of Neurology, Pittsburgh Institute for Neurodegenerative Disorders, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15261, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, U.S. Gov't, Non-P.H.S., Research Support, Non-U.S. Gov't