Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2007-4-3
pubmed:abstractText
Thrombin, a multifunctional serine protease, is neurotoxic in vitro and in vivo. Thrombin has been shown to be increased in Alzheimer's disease (AD) and other neuropathological conditions and could be a mediator of pathological neuronal cell death in the brain. The mechanisms of thrombin-induced neuronal cell death are incompletely understood. The objective of this study is to explore mechanisms that contribute to thrombin-induced neuronal apoptosis focusing on the role of cell cycle regulators and the pro-apoptotic protein Bim (Bcl-2-interacting mediator of cell death) in this process. Our data show that thrombin treatment of primary cerebral cortical cultures results in dose-dependent apoptotic cell death. Exposure of neuronal cultures to thrombin leads to induction of cell cycle proteins cyclin D1 and cyclin E, at both mRNA and protein levels. In addition, thrombin treatment causes the appearance of cyclin-dependent kinase 4 (cdk4) and expression of the pro-apoptotic protein Bim. Inhibition of cdk4 prevents both induction of Bim expression and thrombin-induced neuronal apoptosis. These data demonstrate that thrombin-induced apoptosis proceeds via cell cycle activation involving cdk4 resulting in induction of Bim. Thus, cell cycle proteins could be therapeutic targets in diseases such as AD where thrombin has been implicated.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
0022-3042
pubmed:author
pubmed:issnType
Print
pubmed:volume
101
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
498-505
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:17254021-Alzheimer Disease, pubmed-meshheading:17254021-Animals, pubmed-meshheading:17254021-Apoptosis, pubmed-meshheading:17254021-Apoptosis Regulatory Proteins, pubmed-meshheading:17254021-Cell Cycle Proteins, pubmed-meshheading:17254021-Cells, Cultured, pubmed-meshheading:17254021-Cerebral Cortex, pubmed-meshheading:17254021-Cyclin D1, pubmed-meshheading:17254021-Cyclin-Dependent Kinase 4, pubmed-meshheading:17254021-Dose-Response Relationship, Drug, pubmed-meshheading:17254021-Membrane Proteins, pubmed-meshheading:17254021-Nerve Degeneration, pubmed-meshheading:17254021-Neurodegenerative Diseases, pubmed-meshheading:17254021-Neurons, pubmed-meshheading:17254021-Proto-Oncogene Proteins, pubmed-meshheading:17254021-RNA, Messenger, pubmed-meshheading:17254021-Rats, pubmed-meshheading:17254021-Thrombin
pubmed:year
2007
pubmed:articleTitle
Cyclin D1, cdk4, and Bim are involved in thrombin-induced apoptosis in cultured cortical neurons.
pubmed:affiliation
Garrison Institute on Aging and Department of Neuropsychiatry and Behavioral Sciences, Texas Tech University Health Sciences Center, Lubbock, Texas 79430, USA.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural