Year: 2010
Type: article
Abstract: Alzheimer's disease is a major cause of dementia for which treatments remain unsatisfactory. Cyclin-dependent kinase 5 (CDK5) is a relevant kinase that has been hypothesized to contribute to the tau pathology. Several classes of chemical inhibitors for CDK5 have been developed, but they generally lack the specificity to distinguish among various ATP-dependent kinases. Therefore, the efficacy of these compounds when tested in animal models cannot definitively be attributed to an effect on CDK5. However, RNA interference (RNAi) targeting of CDK5 is specific and can be used to validate CDK5 as a possible treatment target. We delivered a CDK5 RNAi by lentiviral or adenoassociated viral vectors and analyzed the results in vitro and in vivo. Silencing of CDK5 reduces the phosphorylation of tau in primary neuronal cultures and in the brain of wild-type C57BL/6 mice. Furthermore, the knockdown of CDK5 strongly decreased the number of neurofibrillary tangles in the hippocampi of triple-transgenic mice (3×Tg-AD mice). Our data suggest that this downregulation may be attributable to the reduction of the CDK5 availability in the tissue, without affecting the CDK5 kinase activity. In summary, our findings validate CDK5 as a reasonable therapeutic target for ameliorating tau pathology.
Source: Journal of Neuroscience
Language: English
Subfield: Cellular and Molecular Neuroscience
Field: Neuroscience
Domain: Life Sciences
Open Access status: hybrid
Funders: National Science Foundation, Departamento Administrativo de Ciencia, Tecnología e Innovación (COLCIENCIAS), Universidad de Antioquia, National Institutes of Health, National Institute on Aging, National Heart, Lung, and Blood Institute, Fogarty International Center, National Institute of Neurological Disorders and Stroke
Awards: Development of RNAi as Treatment for Neurodegeneration, III-CXT-Large: Working with Uncertain Data in Exploring Scientific Images, Development of RNAi as Treatment for Neurodegeneration, G2521347020, Information Technology Research (ITR): Next-Generation Bio-Molecular Imaging and Information Discovery, RNAi for Dominant Neurological Disease, CISE Research Infrastructure: Digital Campus: Scalable Information Services on a Campus-wide Wireless Network, G5426593556, Cardiovascular Institutional Research Fellowship, G8729475213
OpenAlex ID: W2032306001
