Rees R P, Bunge M B, Bunge R P
J Cell Biol. 1976 Feb;68(2):240-63. doi: 10.1083/jcb.68.2.240.
Our object was to characterize the morphological changes occurring in pre- and postsynaptic elements during their initial contact and subsequent maturation into typical synaptic profiles. Neurons from superior cervical ganglia (SCG) of perinatal rats were freed of their supporting cells and established as isolated cells in culture. To these were added explants of embryonic rat thoracic spinal cord to allow interaction between outgrowing cord neurites and the isolated autonomic neurons. Time of initial contact was assessed by light microscopy; at timed intervals thereafter, cultures were fixed for electron microscopy. Upon contact, growth cone filopodia became extensively applied to the SCG neuronal plasmalemma and manifested numerous punctate regions in which the apposing plasma membranes were separated by only 7-10 nm. The Golgi apparatus of the target neuron hypertrophied, and its production of coated vesicles increased. Similar vesicles were seen in continuity with the SCG plasmalemma near the close contact site; their apparent contribution of a region of postsynaptic membrane with undercoating was considered to be the first definitive sign of synapse formation. Tracer work with peroxidase and ferritin confirmed that the traffic of coated vesicles within the neuronal soma is largely from Golgi region to somal surface. Subsequent to the appearance of postsynaptic density, the form and content of the growth cone was altered by the loss of filopodia and the appearance of synaptic vesicles which gradually became clustered opposite the postsynaptic density. As the synapse matured, synaptic vesicles increased in number, cleft width and content increased, presynaptic density appeared, branched membranous reticulum became greatly diminished, and most lysosomal structures disappeared. Coated vesicles continued to be associated with the postsynaptic membrane at all stages of maturation. The incorporation of Golgi-derived vesicles into discrete regions of the cell membrane could provide the mechanism for confining specific characteristics of the neuronal membrane to the synaptic region.
我们的目的是描述突触前和突触后元件在最初接触以及随后成熟为典型突触形态过程中发生的形态学变化。围产期大鼠颈上神经节(SCG)的神经元与其支持细胞分离,并在培养中建立为分离的细胞。向这些细胞中添加胚胎大鼠胸段脊髓的外植体,以使脊髓神经突的生长与分离的自主神经元相互作用。通过光学显微镜评估最初接触的时间;此后在设定的时间间隔,将培养物固定用于电子显微镜检查。接触时,生长锥丝状伪足广泛贴附于SCG神经元质膜,并表现出许多点状区域,其中相对的质膜仅相隔7-10纳米。靶神经元的高尔基体肥大,其包被小泡的产生增加。在紧密接触部位附近与SCG质膜连续处可见类似的小泡;它们对具有下层包被的突触后膜区域的明显贡献被认为是突触形成的第一个明确迹象。用过氧化物酶和铁蛋白进行的示踪研究证实,神经元胞体内包被小泡的运输主要是从高尔基体区域到胞体表面。突触后致密物出现后,生长锥的形态和内容物因丝状伪足的丧失和突触小泡的出现而改变,突触小泡逐渐聚集在突触后致密物的对面。随着突触成熟,突触小泡数量增加,裂隙宽度和内容物增加,突触前致密物出现,分支的膜性网状结构大大减少,大多数溶酶体结构消失。在成熟的各个阶段,包被小泡继续与突触后膜相关联。将高尔基体衍生的小泡并入细胞膜的离散区域可以提供将神经元膜的特定特征限制在突触区域的机制。