Tzounopoulos T, Janz R, Südhof T C, Nicoll R A, Malenka R C
Department of Psychiatry, University of California, San Francisco 94143, USA.
Neuron. 1998 Oct;21(4):837-45. doi: 10.1016/s0896-6273(00)80599-1.
Mossy fiber synapses on hippocampal CA3 pyramidal cells, in addition to expressing an NMDA receptor-independent form of long-term potentiation (LTP), have recently been shown to express a novel presynaptic form of long-term depression (LTD). We have studied the mechanisms underlying mossy fiber LTD and present evidence that it is triggered, at least in part, by a metabotropic glutamate receptor-mediated decrease in adenylyl cyclase activity, which leads to a decrease in the activity of the cAMP-dependent protein kinase (PKA) and a reversal of the presynaptic processes responsible for mossy fiber LTP. The bidirectional control of synaptic strength at mossy fiber synapses by activity therefore appears to be due to modulation of the cAMP-PKA signaling pathway in mossy fiber boutons.
海马CA3锥体细胞上的苔藓纤维突触,除了表达一种不依赖NMDA受体的长时程增强(LTP)形式外,最近还被证明表达一种新型的突触前长时程抑制(LTD)形式。我们研究了苔藓纤维LTD的潜在机制,并提供证据表明它至少部分是由代谢型谷氨酸受体介导的腺苷酸环化酶活性降低所触发的,这导致cAMP依赖性蛋白激酶(PKA)的活性降低,并逆转了负责苔藓纤维LTP的突触前过程。因此,活动对苔藓纤维突触处突触强度的双向控制似乎是由于苔藓纤维终扣中cAMP-PKA信号通路的调节。