Zhang Jing-ming, Wang Hui-kun, Ye Chang-quan, Ge Wooping, Chen Yiren, Jiang Zheng-lin, Wu Chien-ping, Poo Mu-ming, Duan Shumin
Institute of Neuroscience, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, 200031 China.
Neuron. 2003 Dec 4;40(5):971-82. doi: 10.1016/s0896-6273(03)00717-7.
Extracellular ATP released from axons is known to assist activity-dependent signaling between neurons and Schwann cells in the peripheral nervous system. Here we report that ATP released from astrocytes as a result of neuronal activity can also modulate central synaptic transmission. In cultures of hippocampal neurons, endogenously released ATP tonically suppresses glutamatergic synapses via presynaptic P2Y receptors, an effect that depends on the presence of cocultured astrocytes. Glutamate release accompanying neuronal activity also activates non-NMDA receptors of nearby astrocytes and triggers ATP release from these cells, which in turn causes homo- and heterosynaptic suppression. In CA1 pyramidal neurons of hippocampal slices, a similar synaptic suppression was also produced by adenosine, an immediate degradation product of ATP released by glial cells. Thus, neuron-glia crosstalk may participate in activity-dependent synaptic modulation.
已知轴突释放的细胞外ATP有助于外周神经系统中神经元与施万细胞之间的活性依赖性信号传导。在此我们报告,神经元活动导致星形胶质细胞释放的ATP也可调节中枢突触传递。在海马神经元培养物中,内源性释放的ATP通过突触前P2Y受体持续抑制谷氨酸能突触,这一效应取决于共培养的星形胶质细胞的存在。伴随神经元活动的谷氨酸释放还激活附近星形胶质细胞的非NMDA受体并触发这些细胞释放ATP,进而导致同突触和异突触抑制。在海马切片的CA1锥体神经元中,腺苷(胶质细胞释放的ATP的直接降解产物)也产生了类似的突触抑制。因此,神经元与胶质细胞的相互作用可能参与活性依赖性突触调节。