Yang Yongjie, Gozen Oguz, Watkins Andrew, Lorenzini Ileana, Lepore Angelo, Gao Yuanzheng, Vidensky Svetlana, Brennan Jean, Poulsen David, Won Park Jeong, Li Jeon Noo, Robinson Michael B, Rothstein Jeffrey D
Department of Neurology and Neuroscience, Johns Hopkins University, Baltimore, MD 21287, USA.
Neuron. 2009 Mar 26;61(6):880-94. doi: 10.1016/j.neuron.2009.02.010.
The neuron-astrocyte synaptic complex is a fundamental operational unit of the nervous system. Astroglia regulate synaptic glutamate, via neurotransmitter transport by GLT1/EAAT2. Astroglial mechanisms underlying this essential neuron-glial communication are not known. We now show that presynaptic terminals regulate astroglial synaptic functions, GLT1/EAAT2, via kappa B-motif binding phosphoprotein (KBBP), the mouse homolog of human heterogeneous nuclear ribonucleoprotein K (hnRNP K), which binds the GLT1/EAAT2 promoter. Neuron-stimulated KBBP is required for GLT1/EAAT2 transcriptional activation and is responsible for astroglial alterations in neural injury. Denervation of neuron-astrocyte signaling by corticospinal tract transection, ricin-induced motor neuron death, or neurodegeneration in amyotrophic lateral sclerosis all result in reduced astroglial KBBP expression and transcriptional dysfunction of astroglial transporter expression. Presynaptic elements dynamically coordinate normal astroglial function and also provide a fundamental signaling mechanism by which altered neuronal function and injury leads to dysregulated astroglia in CNS disease.
神经元-星形胶质细胞突触复合体是神经系统的基本运作单元。星形胶质细胞通过GLT1/EAAT2进行神经递质转运来调节突触谷氨酸。这种关键的神经元-胶质细胞通讯背后的星形胶质细胞机制尚不清楚。我们现在表明,突触前终末通过κB基序结合磷蛋白(KBBP,人类异质性核糖核蛋白K(hnRNP K)的小鼠同源物,其与GLT1/EAAT2启动子结合)来调节星形胶质细胞的突触功能和GLT1/EAAT2。神经元刺激的KBBP是GLT1/EAAT2转录激活所必需的,并且是神经损伤中星形胶质细胞改变的原因。皮质脊髓束横断、蓖麻毒素诱导的运动神经元死亡或肌萎缩侧索硬化症中的神经变性导致的神经元-星形胶质细胞信号去神经支配,均会导致星形胶质细胞KBBP表达降低以及星形胶质细胞转运体表达的转录功能障碍。突触前元件动态协调正常的星形胶质细胞功能,并且还提供了一种基本的信号机制,通过该机制,神经元功能改变和损伤会导致中枢神经系统疾病中星形胶质细胞功能失调。