Regulation of dendritogenesis via a lipid-raft-associated Ca2+/calmodulin-dependent protein kinase CLICK-III/CaMKIgamma

Ca(2+) signaling plays a central role in activity-dependent regulation of dendritic arborization, but key molecular mechanisms downstream of calcium elevation remain poorly understood. Here we show that the C-terminal region of the Ca(2+)/calmodulin-dependent protein kinase CLICK-III (CL3)/CaMKIgamm...

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Veröffentlicht in:Neuron (Cambridge, Mass.) Mass.), 2007-06, Vol.54 (5), p.755-770
Hauptverfasser: Takemoto-Kimura, Sayaka, Ageta-Ishihara, Natsumi, Nonaka, Mio, Adachi-Morishima, Aki, Mano, Tatsuo, Okamura, Michiko, Fujii, Hajime, Fuse, Toshimitsu, Hoshino, Mikio, Suzuki, Shingo, Kojima, Masami, Mishina, Masayoshi, Okuno, Hiroyuki, Bito, Haruhiko
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Sprache:eng
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Zusammenfassung:Ca(2+) signaling plays a central role in activity-dependent regulation of dendritic arborization, but key molecular mechanisms downstream of calcium elevation remain poorly understood. Here we show that the C-terminal region of the Ca(2+)/calmodulin-dependent protein kinase CLICK-III (CL3)/CaMKIgamma, a membrane-anchored CaMK, was uniquely modified by two sequential lipidification steps: prenylation followed by a kinase-activity-regulated palmitoylation. These modifications were essential for CL3 membrane anchoring and targeting into detergent-resistant lipid microdomains (or rafts) in the dendrites. We found that CL3 critically contributed to BDNF-stimulated dendritic growth. Raft insertion of CL3 specifically promoted dendritogenesis of cortical neurons by acting upstream of RacGEF STEF and Rac, both present in lipid rafts. Thus, CL3 may represent a key element in the Ca(2+)-dependent and lipid-raft-delineated switch that turns on extrinsic activity-regulated dendrite formation in developing cortical neurons.
ISSN:0896-6273