Fried R C, Blaustein M P
J Cell Biol. 1978 Sep;78(3):685-700. doi: 10.1083/jcb.78.3.685.
The morphological features of pinched-off presynaptic nerve terminals (synaptosomes) from rat brain were examined with electron microscope techniques; in many experiments, an extracellular marked (horseradish peroxidase or colloidal thorium dioxide) was included in the incubation media. When incubated in physiological saline, most terminals appeared approximately spherical, and were filled with small (approximately 400-A diameter) "synaptic vesicles"; mitochondria were also present in many of the terminals. In a number of instances the region of synaptic contact, with adhering portions of the postsynaptic cell membrane and postsynaptic density, could be readily discerned. Approximately 20--30% of the terminals in our preparations exhibited clear evidence of damage, as indicated by diffuse distribution of extracellular markers in the cytoplasm; the markers appeared to be excluded from the intraterminal vesicles under these circumstances. The markers were excluded from the cytoplasm in approximately 70--80% of the terminals, which may imply that these terminals have intact plasma membranes. When the terminals were treated with depolarizing agents (veratridine or K-rich media), in the presence of Ca, many new, large (600--900-A diameter) vesicles and some coated vesicles and new vacuoles appeared. When the media contained an extracellular marker, the newly formed structures frequently were labeled with the marker. If the veratridine-depolarized terminals were subsequently treated with tetrodotoxin (to repolarize the terminals) and allowed to "recover" for 60--90 min, most of the large marker-containing vesicles disappeared, and numerous small (approximately 400-A diameter) marker-containing vesicles appeared. These observations are consistent with the idea that pinched-off presynaptic terminals contain all of the machinery necessary for vesicular exocytosis and for the retrieval and recycling of synaptic vesicle membrane. The vesicle membrane appears to be retrieval primarily in the form of large diameter vesicles which are subsequently reprocessed to form new "typical" small-diameter synaptic vesicles.
采用电子显微镜技术检查了取自大鼠脑的掐断型突触前神经末梢(突触体)的形态特征;在许多实验中,孵育培养基中加入了细胞外标记物(辣根过氧化物酶或二氧化钍胶体)。当在生理盐水中孵育时,大多数末梢呈近似球形,充满了小的(直径约400埃)“突触小泡”;许多末梢中也存在线粒体。在许多情况下,能够很容易地辨别出突触接触区域以及突触后细胞膜和突触后致密部的附着部分。我们制备物中约20% - 30%的末梢呈现出明显的损伤迹象,表现为细胞外标记物在细胞质中的弥漫分布;在这种情况下,标记物似乎被排除在末梢内的小泡之外。在约70% - 80%的末梢中,标记物被排除在细胞质之外,这可能意味着这些末梢具有完整的质膜。当末梢在钙离子存在的情况下用去极化剂(藜芦碱或富含钾的培养基)处理时,会出现许多新的、大的(直径600 - 900埃)小泡以及一些有被小泡和新的液泡。当培养基中含有细胞外标记物时,新形成的结构常常被标记物标记。如果随后用河豚毒素处理经藜芦碱去极化的末梢(使末梢复极化)并使其“恢复”60 - 90分钟,大多数含标记物的大的小泡消失,出现许多含标记物的小的(直径约400埃)小泡。这些观察结果与以下观点一致,即掐断型突触前末梢包含囊泡胞吐作用以及突触小泡膜的回收和再循环所需的所有机制。小泡膜似乎主要以大直径小泡的形式回收,随后经过再加工形成新的“典型”小直径突触小泡。