Finkbeiner S, Tavazoie S F, Maloratsky A, Jacobs K M, Harris K M, Greenberg M E
Department of Neurology, Children's Hospital, Boston, Massachusetts 02115, USA.
Neuron. 1997 Nov;19(5):1031-47. doi: 10.1016/s0896-6273(00)80395-5.
Neurotrophins regulate neuronal survival, differentiation, and synaptic function. To understand how neurotrophins elicit such diverse responses, we elucidated signaling pathways by which brain-derived neurotrophic factor (BDNF) activates gene expression in cultured neurons and hippocampal slices. We found, unexpectedly, that the transcription factor cyclic AMP response element-binding protein (CREB) is an important regulator of BDNF-induced gene expression. Exposure of neurons to BDNF stimulates CREB phosphorylation and activation via at least two signaling pathways: by a calcium/calmodulin-dependent kinase IV (CaMKIV)-regulated pathway that is activated by the release of intracellular calcium and by a Ras-dependent pathway. These findings reveal a previously unrecognized, CaMK-dependent mechanism by which neurotrophins activate CREB and suggest that CREB plays a central role in mediating neurotrophin responses in neurons.
神经营养因子调节神经元的存活、分化及突触功能。为了解神经营养因子如何引发如此多样的反应,我们阐明了脑源性神经营养因子(BDNF)在培养的神经元和海马切片中激活基因表达的信号通路。出乎意料的是,我们发现转录因子环磷腺苷反应元件结合蛋白(CREB)是BDNF诱导基因表达的重要调节因子。神经元暴露于BDNF会通过至少两条信号通路刺激CREB磷酸化和激活:一条是由细胞内钙释放激活的钙/钙调蛋白依赖性激酶IV(CaMKIV)调节的通路,另一条是Ras依赖性通路。这些发现揭示了一种以前未被认识的、CaMK依赖性的神经营养因子激活CREB的机制,并表明CREB在介导神经元对神经营养因子的反应中起核心作用。