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

被引:102
作者
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 [1 ]
机构
[1] Univ Tokyo, Grad Sch Med, Dept Neurochem, Bunkyo Ku, Tokyo 1130033, Japan
[2] Univ Tokyo, Grad Sch Med, Ctr Integrated Brain Med Sci, Bunkyo Ku, Tokyo 1130033, Japan
[3] Kyoto Univ, Grad Sch Med, Dept Pathol & Tumor Biol, Sakyo Ku, Kyoto 6068501, Japan
[4] AIST, Res Inst Cell Engn, Ikeda, Osaka 5638577, Japan
[5] JST, SORST, Kawaguchi 3320012, Japan
[6] Univ Tokyo, Grad Sch Med, Dept Mol Neurobiol & Pharmacol, Bunkyo Ku, Tokyo 1130033, Japan
关键词
D O I
10.1016/j.neuron.2007.05.021
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Ca2+ 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 Ca2+/calmodulin-dependent protein kinase CLICK-III (CL3)/CaMKl gamma, 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 Ca2+-dependent and lipid-raft-delineated switch that turns on extrinsic activity-regulated dendrite formation in developing cortical neurons.
引用
收藏
页码:755 / 770
页数:16
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