Target-cell-specific facilitation and depression in neocortical circuits

被引:569
作者
Reyes, A
Lujan, R
Rozov, A
Burnashev, N
Somogyi, P
Sakmann, B
机构
[1] Max Planck Inst Med Forsch, Zellphysiol Abt, D-69120 Heidelberg, Germany
[2] Univ Oxford, Dept Pharmacol, MRC, Anat Neuropharmacol Unit, Oxford, England
关键词
D O I
10.1038/1092
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In neocortical circuits, repetitively active neurons evoke unitary postsynaptic potentials (PSPs) whose peak amplitudes either increase (facilitate) or decrease (depress) progressively. To examine the basis for these different synaptic responses, we made simultaneous recordings from three classes of neurons in cortical layer 2/3. We induced repetitive action potentials in pyramidal cells and recorded the evoked unitary excitatory (E)PSPs in two classes of GABAergic neurons. We observed facilitation of EPSPs in bitufted GABAergic interneurons, many of which expressed somatostatin immunoreactivity. EPSPs recorded from multipolar interneurons, however, showed depression. Some of these neurons were immunopositive for parvalbumin. Unitary inhibitory (I)PSPs evoked by repetitive stimulation of a bitufted neuron also showed a less pronounced but significant difference between the two target neurons. Facilitation and depression involve presynaptic mechanisms, and because a single neuron can express both behaviors simultaneously, we infer that local differences in the molecular structure of presynaptic nerve terminals are induced by retrograde signals from different classes of target neurons. Because bitufted and multipolar neurons both formed reciprocal inhibitory connections with pyramidal cells, the results imply that the balance of activation between two recurrent inhibitory pathways in the neocortex depends on the frequency of action potentials in pyramidal cells.
引用
收藏
页码:279 / 285
页数:7
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