Publication
p39, the Primary Activator for Cyclin-dependent Kinase 5 (Cdk5) in Oligodendroglia, Is Essential for Oligodendroglia Differentiation and Myelin Repair
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- Persistent URL
- Last modified
- 02/20/2025
- Type of Material
- Authors
- Language
- English
- Date
- 2013-06-21
- Publisher
- American Society for Biochemistry and Molecular Biology
- Publication Version
- Copyright Statement
- © 2013 by The American Society for Biochemistry and Molecular Biology, Inc.
- Final Published Version (URL)
- Title of Journal or Parent Work
- ISSN
- 0021-9258
- Volume
- 288
- Issue
- 25
- Start Page
- 18047
- End Page
- 18057
- Grant/Funding Information
- Supported by National Institutes of Health Training Grant T32GM008602.
- This work was supported, in whole or in part, by National Institutes of Health Grants NS053905 (to Y. F.), NS053905-03S2 (to F. C.), and MH083711, DA033485, and NS073855 (to J. A. B.). This work was also supported by National Multiple Sclerosis Society Grant NMSSRG 4010-A (to Y. F.) and an Emory University Research Committee grant (to Y. F.).
- The FACS sorting facility at the University of Kentucky is supported in part by the National Institutes of Health Shared Instrument Program (S10 RR026827-01A1).
- Abstract
- Background: Cyclin-dependent kinase 5 (Cdk5) is crucial for brain development. Results: In contrast to neurons that utilize p35 as the primary Cdk5 activator, oligodendroglia employ p39-dependent Cdk5 activation to advance differentiation and myelin repair. Conclusion: p39 is the primary Cdk5 activator in oligodendroglia, essential for oligodendroglia development. Significance: Our study revealed distinct mechanisms controlling Cdk5 activity in neurons and oligodendroglia.
- Author Notes
- Keywords
- Research Categories
- Health Sciences, General
- Biology, Molecular
- Chemistry, Biochemistry
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