Unified mechanisms of Ca2+ regulation across the Ca2+ channel family

被引:256
作者
Liang, HY
DeMaria, CD
Erickson, MG
Mori, MX
Alseikhan, BA
Yue, DT [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Biomed Engn, Ca Signals Lab, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Neurosci, Ca Signals Lab, Baltimore, MD 21205 USA
[3] Georgetown Univ, Off Technol Licensing, Washington, DC 20057 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S0896-6273(03)00560-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
L-type (Ca(V)1.2) and P/Q-type (Ca(V)2.1) calcium channels possess lobe-specific CaM regulation, where Call binding to one or the other lobe of CaM triggers regulation, even with inverted polarity of modulation between channels. Other major members of the Ca(V)1-2 channel family, R-type (Ca(V)2.3) and N-type (Ca(V)2.2), have appeared to lack such CaM regulation. We report here that R- and N-type channels undergo Ca2+-dependent inactivation, which is mediated by the CaM N-terminal lobe and present only with mild Ca2+ buffering (0.5 mM EGTA) characteristic of many neurons. These features, together with the CaM regulatory profiles of L- and P/Q-type channels, are consistent with a simplifying principle for CaM signal detection in Ca(V)1-2 channels-independent of channel context, the N- and C-terminal lobes of CaM appear invariably specialized for decoding local versus global Ca2+ activity, respectively.
引用
收藏
页码:951 / 960
页数:10
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