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Cyclin-dependent kinases in neural development and degeneration
- Source :
- Journal of Alzheimer's Disease. 5:329-335
- Publication Year :
- 2003
- Publisher :
- IOS Press, 2003.
-
Abstract
- There is increasing evidence suggesting that cyclin-dependent kinases (Cdks) that normally regulate cell cycle progression may also be involved in the pathogenesis of neurodegenerative disorders and in the apoptotic death of neurons subjected to various insults. Deregulation of Cdks has been observed in an increasing number of neurological disorders, including Alzheimer's and Parkinson's diseases as well as amyotrophic lateral sclerosis (ALS). Unchecked expression of these proteins can potently induce apoptotic or necrotic neuronal cell death. Cdks initiate death pathways by derepressing E2F-1/pRb-dependent transcription at neuronal G1/S checkpoint. On the contrary, deregulation of Cdk5, which is not involved in cell cycle control, contributes to neurodegeneration by altering the phosphorylation state of non-membrane-associated proteins. This review describes work indicating Cdks' roles in the nervous system and how they may cogitate in leading neurons to their demise.
- Subjects :
- Programmed cell death
Apoptosis
Cell Cycle Proteins
Gene Expression Regulation, Enzymologic
Alzheimer Disease
Cyclin-dependent kinase
medicine
Animals
Humans
Amyotrophic lateral sclerosis
biology
Kinase
General Neuroscience
Cyclin-dependent kinase 5
Cell Cycle
Neurodegeneration
General Medicine
medicine.disease
Cyclin-Dependent Kinases
E2F Transcription Factors
Cell biology
DNA-Binding Proteins
Psychiatry and Mental health
Clinical Psychology
Nerve Degeneration
biology.protein
Phosphorylation
biological phenomena, cell phenomena, and immunity
Geriatrics and Gerontology
Neural development
Cell Division
E2F1 Transcription Factor
Transcription Factors
Subjects
Details
- ISSN :
- 18758908 and 13872877
- Volume :
- 5
- Database :
- OpenAIRE
- Journal :
- Journal of Alzheimer's Disease
- Accession number :
- edsair.doi.dedup.....ab17fc4d71db0af776f6364df560d3cb
- Full Text :
- https://doi.org/10.3233/jad-2003-5409