Tischner K
J Anat. 1977 Sep;124(Pt 1):83-97.
After 47 3/4 hours in vitro, organotypic cultures of dorsal root ganglia of rat were exposed to horseradish peroxidase at a concentration of 4 mg/ml of nutrient medium for 15 minutes. Observations on the living nerve fibres revealed pinocytotic vesicles in the growth cones which were transported toward the perikarya for several hundreds of micrometer at a rate of 0-5-10 micrometer/min. Electron microscopic sections displayed uptake of peroxidase into the growth cones by means of endocytosis. The enzyme marker was contained in small-sized vesicles, as well as in large vacuoles which measured up to 2 micrometer in diameter. The more proximal parts of the axon contained tiny vesicles which were well below the level of resolution of the light microscope. Pinocytotic phenomena were abundant at the fibre tips, but could also be observed occasionally in the intermediate and more proximal portions of contiguous axons. It is proposed tentatively that the large vacuoles in the distal and intermediate parts of the axon had formed from the small vesicles. Furthermore, it is suggested that the profuse uptake and backward transport of vesicles in these regenerating neurons might be meaningful for the neuron in terms of intercellular and environmental recognition.
在体外培养47又3/4小时后,将大鼠背根神经节的器官型培养物置于浓度为4毫克/毫升营养培养基的辣根过氧化物酶中15分钟。对活神经纤维的观察显示,生长锥中有胞饮小泡,这些小泡以0 - 5 - 10微米/分钟的速度向胞体方向运输数百微米。电子显微镜切片显示,过氧化物酶通过内吞作用被摄取到生长锥中。酶标记物存在于小泡以及直径达2微米的大液泡中。轴突较近端部分含有微小的小泡,其大小远低于光学显微镜的分辨率。胞饮现象在纤维末端大量存在,但在相邻轴突的中间和更近端部分也偶尔可见。初步推测,轴突远端和中间部分的大液泡是由小泡形成的。此外,有人提出,这些再生神经元中大量摄取和逆向运输小泡可能对神经元在细胞间识别和环境识别方面具有重要意义。