Department of Biochemistry, Weill Cornell Medical College, New York, NY 10065, USA.
Neuron. 2010 Sep 9;67(5):797-809. doi: 10.1016/j.neuron.2010.08.003.
CDK5 is an important kinase in nervous system function, controlling neural development and postsynaptic signal integration. Here we show that CDK5 plays a major role in controlling neurotransmitter release. Inhibition of CDK5 activity, by either acute or genetic means, leads to profound potentiation of presynaptic function, including unmasking of previously "silent" synapses. Removal of CDK5 activity additionally unlocks access to the resting synaptic vesicle pool, which normally remains recalcitrant to exocytosis and recycling even following prolonged action potential stimuli. Presynaptic CDK5 levels are additionally severely depleted by chronic neuronal silencing, a treatment that is functionally similar to CDK5 knockdown with regard to presynaptic potentiation. Thus CDK5 appears to be an integral element in presynaptic homeostatic scaling, and the resting vesicle pool appears to provide a potent functional presynaptic homeostatic control parameter. These studies thus pinpoint CDK5 as a major control point for modulation of neurotransmitter release in mammalian neurons.
CDK5 是神经系统功能中一种重要的激酶,控制着神经发育和突触后信号整合。在这里,我们表明 CDK5 在控制神经递质释放方面起着主要作用。通过急性或遗传手段抑制 CDK5 的活性会导致突触前功能的显著增强,包括先前“沉默”突触的揭示。去除 CDK5 的活性还可以解锁对静止突触囊泡池的访问,即使在长时间的动作电位刺激后,该池通常仍然对胞吐和再循环具有抗性。慢性神经元沉默会使突触前 CDK5 水平严重耗竭,这种处理在突触前增强方面与 CDK5 敲低的功能相似。因此,CDK5 似乎是突触前自身稳态调节的一个基本组成部分,而静止囊泡池似乎为有力的功能突触前自身稳态控制参数。这些研究因此确定 CDK5 是调节哺乳动物神经元神经递质释放的主要控制点。