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Please use this identifier to cite or link to this item: http://hdl.handle.net/1783.1/3530
Title: Cyclin-dependent kinase 5 supports neuronal survival through phosphorylation of Bcl-2
Authors: Cheung, Zelda H.
Gong, Ke
Ip, Nancy Y.
Keywords: Apoptosis
p35
Bcl-2
Cdk5
Neuronal survival
Retinal ganglion cells
Issue Date: May-2008
Citation: Journal of Neuroscience, vol. 28, no. 19, May 2008, p. 4872-4877
Abstract: Accumulating evidence indicates that deregulation of cyclin-dependent kinase 5 (Cdk5) activity is associated with apoptosis in various neurodegenerative disease models. Interestingly, recent studies suggest that Cdk5 may also favor neuronal survival. Nonetheless, whether Cdk5 is directly required for neuronal survival during development remains enigmatic. In the current study, we established the pivotal role of Cdk5 in neuronal survival during development by demonstrating that reduction or absence of Cdk5 activity markedly exacerbated neuronal death in cultures and in vivo. Interestingly, the antiapoptotic protein Bcl-2 (B-cell lymphoma protein 2) was identified as a novel substrate of Cdk5. We found that Cdk5-mediated phosphorylation of Bcl-2 at Ser70 was required for the neuroprotective effect of Bcl-2. Intriguingly, inhibition of this phosphorylation conferred proapoptotic property to Bcl-2. Furthermore, overexpression of a Bcl-2 mutant lacking the Cdk5 phosphorylation site abolished the protective effect of Cdk5 re-expression in Cdk5-/- neurons, suggesting that Ser70 phosphorylation of Bcl-2 contributed to Cdk5-mediated neuronal survival. Our observations revealed that Cdk5-mediated Bcl-2 phosphorylation is pivotal for the antiapoptotic effect of Bcl-2 and contributes to the maintenance of neuronal survival by Cdk5. Our study has also identified Cdk5 as a regulator of Bcl-2 function in neuronal apoptosis.
Rights: The Society for Neuroscience is the copyright holder for this article
URI: http://hdl.handle.net/1783.1/3530
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