期刊
JOURNAL OF CELL BIOLOGY
卷 192, 期 5, 页码 813-824出版社
ROCKEFELLER UNIV PRESS
DOI: 10.1083/jcb.201007113
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资金
- NIH [NS34383]
- Institut National de la Sante et de la Recherche Medicale [IRG-2008-239499]
- Fondation pour la Recherche Medicale
- Centre National de la Recherche Scientifique
Kv1 channels are concentrated at specific sites in the axonal membrane, where they regulate neuronal excitability. Establishing these distributions requires regulated dissociation of Kv1 channels from the neuronal trafficking machinery and their subsequent insertion into the axonal membrane. We find that the auxiliary Kv. 2 subunit of Kv1 channels purified from brain is phosphorylated on serine residues 9 and 31, and that cyclin-dependent kinase (Cdk)-mediated phosphorylation at these sites negatively regulates the interaction of Kv beta 2 with the microtubule plus end-tracking protein EB1. Endogenous Cdks, EB1, and Kv. 2 phosphorylated at serine 31 are colocalized in the axons of cultured hippocampal neurons, with enrichment at the axon initial segment (AIS). Acute inhibition of Cdk activity leads to intracellular accumulation of EB1, Kv. 2, and Kv1 channel subunits within the AIS. These studies reveal a new regulatory mechanism for the targeting of Kv1 complexes to the axonal membrane through the reversible Cdk phosphorylation-dependent binding of Kv beta 2 to EB1.
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