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[星形胶质细胞ATP对突触传递的调节作用]

[Regulation by astrocytic ATP of synaptic transmission].

作者信息

Koizumi Schuichi, Inoue Kazuhide

机构信息

Division of Pharmacology, National Institute of Health Sciences.

出版信息

Nihon Yakurigaku Zasshi. 2004 Jun;123(6):389-96. doi: 10.1254/fpj.123.389.

Abstract

Originally ascribed to having only passive roles in the CNS, astrocytes are now known to have an active role in the regulation of synaptic transmission. Neuronal activity can evoke Ca(2+) transients in astrocytes and Ca(2+) transients in astrocytes can evoke changes in neuronal activity. The excitatory neurotransmitter glutamate has been shown to mediate such bi-directional communication between astrocytes and neurons. We demonstrate here that ATP, a primary mediator of intercellular Ca(2+) signaling among astrocytes, also mediates intercellular signaling between astrocytes and neurons in hippocampal cultures. Mechanical stimulation of astrocytes evoked Ca(2+) waves mediated by the release of ATP and activation of P2 receptors. Mechanically evoked Ca(2+) waves led to decreased excitatory glutamatergic synaptic transmission in an ATP-dependent manner. Exogenous application of ATP does not affect post-synaptic glutamatergic responses but decreased pre-synaptic exocytotic events. Finally, we show that astrocytes exhibit spontaneous Ca(2+) oscillations mediated by extracellular ATP and that inhibition of these Ca(2+) responses enhanced excitatory glutamatergic transmission. We therefore conclude that ATP released from astrocytes exerts tonic and activity-dependent down-regulation of synaptic transmission via pre-synaptic mechanisms.

摘要

星形胶质细胞最初被认为在中枢神经系统中仅起被动作用,现在已知它们在突触传递的调节中起积极作用。神经元活动可诱发星形胶质细胞中的Ca(2+)瞬变,而星形胶质细胞中的Ca(2+)瞬变可诱发神经元活动的变化。兴奋性神经递质谷氨酸已被证明可介导星形胶质细胞与神经元之间的这种双向通信。我们在此证明,ATP作为星形胶质细胞间细胞内Ca(2+)信号传导的主要介质,也介导海马培养物中星形胶质细胞与神经元之间的细胞间信号传导。对星形胶质细胞的机械刺激诱发了由ATP释放和P2受体激活介导的Ca(2+)波。机械诱发的Ca(2+)波以ATP依赖的方式导致兴奋性谷氨酸能突触传递减少。外源性应用ATP不影响突触后谷氨酸能反应,但减少突触前胞吐事件。最后,我们表明星形胶质细胞表现出由细胞外ATP介导的自发Ca(2+)振荡,并且抑制这些Ca(2+)反应增强了兴奋性谷氨酸能传递。因此,我们得出结论,星形胶质细胞释放的ATP通过突触前机制对突触传递发挥张力性和活性依赖性下调作用。

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