Major G, Larkman A U, Jonas P, Sakmann B, Jack J J
University Laboratory of Physiology, Oxford, United Kingdom.
J Neurosci. 1994 Aug;14(8):4613-38. doi: 10.1523/JNEUROSCI.14-08-04613.1994.
Tight-seal whole-cell recordings were made from cleaned somata of CA3 pyramidal cells deep in hippocampal slices from 19-21-d-old rats. The cells were filled with biocytin, and their voltage responses to short current pulses were recorded. After washout of initial sag, responses scaled linearly with injected current and were stable over time. The dendritic and axonal arbors of four cells were reconstructed and measured using light microscopy. Dendritic spines and axonal boutons were counted and the additional membrane area was incorporated into the relevant segments. The morphology of each neuron was converted into a detailed branching cable model by assuming values for specific membrane capacitance Cm and resistance Rm, and cytoplasmic resistivity Ri. These parameters were optimized for each cell by directly matching the model's response to that of the real cell by means of a modified weighted least-squares fitting procedure. By comparing the deviations between model and experimental responses to control noise recordings, approximate 95% confidence intervals were established for each parameter. If a somatic shunt was allowed, a wide range of possible Rm values produced acceptable fits. With zero shunt, Cm was 0.7-0.8 microFcm-2, Ri was 170-340 omega cm, and Rm ranged between 120 and 200 k omega cm2. The electrotonic lengths of the basal and oblique dendrites were 0.2-0.3 space constants, and those of the apical tufts were 0.4-0.7 space constants. The steady-state electrical geometry of these cells was therefore compact; average dendritic tip/soma relative synaptic efficacies were > 93% for the basal and oblique dendrites, and > 81% for the tufts. With fast transient synaptic inputs, however, the models produced a wide range of postsynaptic potential shapes and marked filtering of voltage-clamp currents.
对19 - 21日龄大鼠海马切片深处的CA3锥体细胞的清洁胞体进行了全细胞封接记录。细胞用生物素填充,并记录它们对短电流脉冲的电压反应。初始凹陷消除后,反应与注入电流呈线性比例关系,且随时间稳定。使用光学显微镜对四个细胞的树突和轴突分支进行重建和测量。对树突棘和轴突终扣进行计数,并将额外的膜面积纳入相关节段。通过假设特定膜电容Cm、电阻Rm和细胞质电阻率Ri的值,将每个神经元的形态转化为详细的分支电缆模型。通过一种改进的加权最小二乘法拟合程序,使模型的反应与真实细胞的反应直接匹配,从而对每个细胞的这些参数进行优化。通过比较模型与实验对对照噪声记录的反应之间的偏差,为每个参数建立了近似95%的置信区间。如果允许体细胞分流,广泛的可能Rm值都能产生可接受的拟合。在零分流的情况下,Cm为0.7 - 0.8 μF/cm²,Ri为170 - 340 Ω·cm,Rm在120至200 kΩ·cm²之间。基底和斜向树突的电紧张长度为0.2 - 0.3个空间常数,顶树突簇的电紧张长度为0.4 - 0.7个空间常数。因此,这些细胞的稳态电几何结构是紧凑的;基底和斜向树突的平均树突尖端/胞体相对突触效能> 93%,树突簇的> 81%。然而,对于快速瞬态突触输入,模型产生了广泛的突触后电位形状,并对电压钳电流进行了显著滤波。