Deisseroth K, Bito H, Tsien R W
Department of Molecular and Cellular Physiology, Beckman Center for Molecular and Genetic Medicine, Stanford University School of Medicine, California 94305, USA.
Neuron. 1996 Jan;16(1):89-101. doi: 10.1016/s0896-6273(00)80026-4.
Phosphorylation of the transcription factor CREB is thought to be important in processes underlying long-term memory. It is unclear whether CREB phosphorylation can carry information about the sign of changes in synaptic strength, whether CREB pathways are equally activated in neurons receiving or providing synaptic input, or how synapse-to-nucleus communication is mediated. We found that Ca(2+)-dependent nuclear CREB phosphorylation was rapidly evoked by synaptic stimuli including, but not limited to, those that induced potentiation and depression of synaptic strength. In striking contrast, high frequency action potential firing alone failed to trigger CREB phosphorylation. Activation of a submembranous Ca2+ sensor, just beneath sites of Ca2+ entry, appears critical for triggering nuclear CREB phosphorylation via calmodulin and a Ca2+/calmodulin-dependent protein kinase.
转录因子CREB的磷酸化被认为在长期记忆形成过程中起着重要作用。目前尚不清楚CREB磷酸化是否能够携带有关突触强度变化信号的信息,在接受或提供突触输入的神经元中CREB通路是否同样被激活,或者突触到细胞核的通讯是如何介导的。我们发现,包括但不限于那些诱导突触强度增强和减弱的突触刺激,能够快速诱发依赖于Ca(2+)的细胞核CREB磷酸化。与之形成鲜明对比的是,单独的高频动作电位发放并不能触发CREB磷酸化。位于Ca2+进入位点正下方的膜下Ca2+传感器的激活,似乎对于通过钙调蛋白和一种Ca2+/钙调蛋白依赖性蛋白激酶触发细胞核CREB磷酸化至关重要。