Hanganu Ileana L, Kilb Werner, Luhmann Heiko J
Institute of Neurophysiology, Heinrich-Heine-University Düsseldorf, D-40001 Düsseldorf, Germany.
J Neurosci. 2002 Aug 15;22(16):7165-76. doi: 10.1523/JNEUROSCI.22-16-07165.2002.
Subplate neurons (SPn) play an important role in the formation of thalamocortical connections during early development and show glutamatergic and GABAergic spontaneous synaptic activity. We characterized these synaptic inputs by performing whole-cell recordings from SPn in somatosensory cortical slices of postnatal day 0-3 rats. At -70 mV, electrical stimulation of the thalamocortical afferents elicited in 68% of the SPn a monosynaptic CNQX-sensitive postsynaptic current (PSC). These fast PSCs were mediated by AMPA receptors, because they were prolonged by cyclothiazide and blocked by GYKI 52466. On membrane depolarization, thalamocortical stimulation elicited in 50% of the cells an additional slow monosynaptic component mediated by NMDA receptors. Stimulation of the cortical plate evoked in 72% of SPn a monosynaptic AMPA receptor-mediated PSC with an additional NMDA component at depolarized membrane potentials and in 40% of the investigated cells polysynaptic responses, depending on GABA(A) and NMDA receptors. Stimulation of the subplate elicited in 67% of SPn a monosynaptic dual-component PSC mediated by AMPA and NMDA receptors activated at -70 mV and in 12% of SPn a monosynaptic single-component PSC mediated by AMPA receptors with an additional NMDA component activated at depolarized membrane potentials. A monosynaptic GABAergic response could be observed in 68% of SPn after stimulation of the subplate. In gramicidin-perforated patch recordings, bath application of GABA caused membrane depolarization to -40 mV and elicited action potentials. These results demonstrate that SPn receive distinct functional synaptic inputs arising from the thalamus, cortical plate, and subplate, indicating that SPn are capable of integrating and processing information from cortical and subcortical regions.
在早期发育过程中,板下神经元(SPn)在丘脑皮质连接的形成中发挥重要作用,并表现出谷氨酸能和γ-氨基丁酸能的自发突触活动。我们通过对出生后0 - 3天大鼠体感皮质切片中的SPn进行全细胞记录,来表征这些突触输入。在 -70 mV时,对丘脑皮质传入纤维的电刺激在68%的SPn中引发了一种单突触的、对CNQX敏感的突触后电流(PSC)。这些快速PSC由AMPA受体介导,因为它们会被环噻嗪延长,并被GYKI 52466阻断。在膜去极化时,丘脑皮质刺激在50%的细胞中引发了另一种由NMDA受体介导的缓慢单突触成分。对皮质板的刺激在72%的SPn中引发了一种单突触的、由AMPA受体介导的PSC,并在去极化膜电位时伴有另一种NMDA成分,在40%的被研究细胞中引发了多突触反应,这取决于γ-氨基丁酸A(GABA(A))和NMDA受体。对板下的刺激在67%的SPn中引发了一种由AMPA和NMDA受体介导的单突触双成分PSC,在 -70 mV时激活,在12%的SPn中引发了一种由AMPA受体介导的单突触单成分PSC,并在去极化膜电位时伴有另一种NMDA成分激活。在刺激板下后,68%的SPn中可观察到单突触GABA能反应。在短杆菌肽穿孔膜片钳记录中,向浴槽中加入GABA导致膜去极化至 -40 mV并引发动作电位。这些结果表明,SPn接受来自丘脑、皮质板和板下的不同功能性突触输入,表明SPn能够整合和处理来自皮质和皮质下区域的信息。