Poisbeau P, René F, Egles C, Félix J M, Feltz P, Schlichter R
Laboratoire de Neurophysiologie et de Neurobiologie des Systèmes Endocrines, Strasbourg, France.
J Neurosci. 1996 Aug 15;16(16):4835-45. doi: 10.1523/JNEUROSCI.16-16-04835.1996.
Rat hypothalamic neurons and endocrine cells from the intermediate lobe of the pituitary were grown in dissociated coculture. Neurons positively stained with an antibody against glutamate decarboxylase established apparent contacts with the alpha-melanocyte-stimulating hormone-positive endocrine cells. These sites of contact were intensely labeled with an antibody against the synaptic protein synapsin I and displayed ultrastructural features characteristic of synapses. Using patch-clamp recordings, we have demonstrated that these contacts correspond to functional GABAergic synapses. The synaptic currents were blocked reversibly by bicuculline (5 microM) and SR95531 (5 microM), two competitive antagonists of the GABAA receptor. At a holding potential of -60 mV, spontaneously occurring IPSCs (s-IPSCs) had small amplitudes (10-100 pA), whereas electrically evoked IPSCs (ee-IPSCs) had amplitudes up to 1 nA. The rise times of both types of IPSCs were fast ( < or = 1 msec), and their decaying phases were fitted in most cases with a single exponential function (time constant 50 msec). The amplitude distribution of s-IPSCs did not reveal clear, equally spaced peaks and was little affected by tetrodotoxin, suggesting that most s-IPSCs were miniature IPSCs. Reduction of extracellular calcium concentration to 0.3 mM induced a marked decrease in s-IPSC frequency and revealed a single amplitude peak at 10 pA, suggesting that a single quantum of GABA activates 8-10 GABAA channels. Thus, our preparation might be an interesting model to study different aspects of synapse formation between a central neuron and its target as well as the fundamental mechanisms of synaptic transmission at central synapses.
将大鼠下丘脑神经元与来自垂体中间叶的内分泌细胞进行解离共培养。用抗谷氨酸脱羧酶抗体阳性染色的神经元与α-黑素细胞刺激素阳性的内分泌细胞建立了明显的接触。这些接触部位被抗突触蛋白突触素I的抗体强烈标记,并表现出突触特有的超微结构特征。通过膜片钳记录,我们证明这些接触对应于功能性GABA能突触。突触电流被GABAA受体的两种竞争性拮抗剂荷包牡丹碱(5微摩尔)和SR95531(5微摩尔)可逆性阻断。在-60毫伏的钳制电位下,自发产生的抑制性突触后电流(s-IPSCs)幅度较小(10-100皮安),而电诱发的抑制性突触后电流(ee-IPSCs)幅度可达1纳安。两种类型的抑制性突触后电流的上升时间都很快(≤1毫秒),并且在大多数情况下其衰减相符合单指数函数(时间常数50毫秒)。s-IPSCs的幅度分布没有显示出清晰、等间距的峰值,并且受河豚毒素的影响很小,这表明大多数s-IPSCs是微小抑制性突触后电流。将细胞外钙浓度降低到0.3毫摩尔会导致s-IPSC频率显著降低,并在10皮安处显示出一个单一的幅度峰值,这表明单个GABA量子激活8-10个GABAA通道。因此,我们的制备方法可能是研究中枢神经元与其靶标之间突触形成的不同方面以及中枢突触处突触传递基本机制的一个有趣模型。