Jeon Daejong, Yang Yu-Mi, Jeong Myung-Jin, Philipson Kenneth D, Rhim Hyewhon, Shin Hee-Sup
National Creative Research Initiative Center for Calcium & Learning, Korea Institute of Science and Technology, 136-791, Seoul, South Korea.
Neuron. 2003 Jun 19;38(6):965-76. doi: 10.1016/s0896-6273(03)00334-9.
The plasma membrane Na(+)/Ca(2+) exchanger (NCX) plays a role in regulation of intracellular Ca(2+) concentration via the forward mode (Ca(2+) efflux) or the reverse mode (Ca(2+) influx). To define the physiological function of the exchanger in vivo, we generated mice deficient for NCX2, the major isoform in the brain. Mutant hippocampal neurons exhibited a significantly delayed clearance of elevated Ca(2+) following depolarization. The frequency threshold for LTP and LTD in the hippocampal CA1 region was shifted to a lowered frequency in the mutant mice, thereby favoring LTP. Behaviorally, the mutant mice exhibited enhanced performance in several hippocampus-dependent learning and memory tasks. These results demonstrate that NCX2 can be a temporal regulator of Ca(2+) homeostasis and as such is essential for the control of synaptic plasticity and cognition.
质膜钠/钙交换体(NCX)通过正向模式(钙外流)或反向模式(钙内流)在调节细胞内钙浓度方面发挥作用。为了确定该交换体在体内的生理功能,我们培育出了大脑中主要亚型NCX2缺失的小鼠。突变的海马神经元在去极化后表现出升高的钙清除明显延迟。突变小鼠海马CA1区的长时程增强(LTP)和长时程抑制(LTD)的频率阈值向低频偏移,从而有利于LTP。在行为上,突变小鼠在几项依赖海马体的学习和记忆任务中表现出增强的能力。这些结果表明,NCX2可以作为钙稳态的时间调节器,因此对于控制突触可塑性和认知至关重要。