Department of Pharmacology, Emory University, Atlanta, Georgia 30322, USA.
J Neurosci. 2010 Apr 14;30(15):5125-35. doi: 10.1523/JNEUROSCI.4367-09.2010.
Ca(v)1 (L-type) channels and calmodulin-dependent protein kinase II (CaMKII) are key regulators of Ca(2+) signaling in neurons. CaMKII directly potentiates the activity of Ca(v)1.2 and Ca(v)1.3 channels, but the underlying molecular mechanisms are incompletely understood. Here, we report that the CaMKII-associated protein densin is required for Ca(2+)-dependent facilitation of Ca(v)1.3 channels. While neither CaMKII nor densin independently affects Ca(v)1.3 properties in transfected HEK293T cells, the two together augment Ca(v)1.3 Ca(2+) currents during repetitive, but not sustained, depolarizing stimuli. Facilitation requires Ca(2+), CaMKII activation, and its association with densin, as well as densin binding to the Ca(v)1.3 alpha(1) subunit C-terminal domain. Ca(v)1.3 channels and densin are targeted to dendritic spines in neurons and form a complex with CaMKII in the brain. Our results demonstrate a novel mechanism for Ca(2+)-dependent facilitation that may intensify postsynaptic Ca(2+) signals during high-frequency stimulation.
钙通道 (L 型) 和钙调蛋白依赖性蛋白激酶 II (CaMKII) 是神经元钙离子信号的关键调节因子。CaMKII 可直接增强 Ca(v)1.2 和 Ca(v)1.3 通道的活性,但潜在的分子机制尚不完全清楚。本研究报道钙调蛋白激酶 II 相关蛋白 densin 是 Ca(2+) 依赖性增强 Ca(v)1.3 通道的必需蛋白。虽然 CaMKII 或 densin 本身都不会影响转染的 HEK293T 细胞中 Ca(v)1.3 通道的特性,但两者共同增强了重复但非持续去极化刺激期间的 Ca(v)1.3 钙离子电流。该增强作用需要 Ca(2+)、CaMKII 激活及其与 densin 的结合,以及 densin 与 Ca(v)1.3 α1 亚基 C 端结构域的结合。Ca(v)1.3 通道和 densin 被靶向到神经元的树突棘,并在脑中与 CaMKII 形成复合物。我们的研究结果证明了一种新的 Ca(2+) 依赖性增强机制,该机制可能在高频刺激期间增强突触后钙离子信号。