Neale E A, Macdonald R L, Nelson P G
Brain Res. 1978 Aug 25;152(2):265-82. doi: 10.1016/0006-8993(78)90255-x.
Synaptic interactions between spinal cord neurons grown in dissociated cell culture were studied electrophysiologically, and presynaptic cells were subsequently injected by intracellular iontophoresis with horseradish peroxidase (HRP). Following histochemical processing, injected cells were filled with dense reaction product which facilitated the light and electron microscopic identification of the individual physiologically typed neurons. This technique applied to neurons in monolayer culture allowed the visualization of complex intercellular relationships in essentially two dimensions. The number and distribution of morphologically defined synaptic contacts was determined for correlation with individual evoked postsynaptic potentials. HRP-filling of inhibitory and excitatory neurons revealed differences with respect to cellular geometry, axonal projection, and the number, location and ultrastructure of synaptic contacts.
对解离细胞培养中生长的脊髓神经元之间的突触相互作用进行了电生理研究,随后通过细胞内离子电泳向突触前细胞注射辣根过氧化物酶(HRP)。经过组织化学处理后,注射的细胞充满了密集的反应产物,这有助于在光学显微镜和电子显微镜下识别单个生理类型的神经元。将该技术应用于单层培养的神经元,可以在基本上二维的层面上观察复杂的细胞间关系。确定形态学定义的突触接触的数量和分布,以便与单个诱发的突触后电位进行关联。对抑制性和兴奋性神经元进行HRP填充后,发现它们在细胞几何形状、轴突投射以及突触接触的数量、位置和超微结构方面存在差异。