Playford D E, Dunlop S A
Department of Psychology, University of Western Australia, Nedlands.
J Comp Neurol. 1993 Jul 1;333(1):83-93. doi: 10.1002/cne.903330107.
We have examined the sequence of myelination along the optic nerve of the frog Litoria (Hyla) moorei from early tadpole life to adulthood. Myelinated axons were counted in electron micrographs of transverse sections taken from behind the eye, at the optic foramen and the chiasm. In tadpoles, myelinated axon numbers were significantly higher at the foramen than at the other levels. By metamorphic climax, numbers had risen at all three levels but more so behind the eye and at the chiasm to become approximately equal along the nerve. After metamorphosis, there was a dramatic increase in myelinated axon numbers, but another pattern was seen; in frogs of 5 cm and 7 cm body length, counts were significantly higher at the chiasm than at the foramen and lowest behind the eye. Thereafter, myelinated axon numbers stabilized at the chiasm but increased behind the eye and at the foramen so that in the most mature stage for this species, 9 cm adults, counts were again similar at the three levels. In addition, total axon numbers, that is, myelinated plus unmyelinated, were assessed from electron micrographs and increased from approximately 8,500 in early tadpoles to 0.65 million in fully mature adults. The proportion of axons that were myelinated showed two peaks, one before and the other after metamorphosis. Measurements of axon diameters from electron micrographs suggested that there was a critical diameter for myelination of 0.3 microns before, and of 0.5 microns after metamorphosis. The data indicate that there is a biphasic sequence of myelination of optic axons, the first phase being pre-metamorphic and the second post-metamorphic. The first phase is initiated at the foramen, and then extends both towards the eye and chiasm and continues until metamorphic climax. During the second phase, myelination originates at the chiasm, spreads towards the eye, and is complete only in the most mature adults. The critical diameter for myelination is smaller in the first phase than in the second.
我们研究了从早期蝌蚪阶段到成年期,莫氏雨滨蛙(Litoria (Hyla) moorei)视神经上的髓鞘形成顺序。在取自眼球后方、视神经孔和视交叉处的横切电子显微照片中对有髓轴突进行计数。在蝌蚪中,视神经孔处的有髓轴突数量显著高于其他部位。到变态高峰期,所有三个部位的数量都有所增加,但眼球后方和视交叉处增加得更多,使得沿神经各处数量大致相等。变态后,有髓轴突数量急剧增加,但呈现出另一种模式;在体长5厘米和7厘米的青蛙中,视交叉处的计数显著高于视神经孔处,而眼球后方最低。此后,视交叉处的有髓轴突数量稳定下来,但眼球后方和视神经孔处的数量增加,以至于在该物种最成熟阶段,即9厘米的成年蛙中,三个部位的计数再次相似。此外,从电子显微照片评估了总轴突数量,即有髓和无髓轴突总数,其从早期蝌蚪时的约8500个增加到完全成熟成年蛙时的65万个。有髓轴突的比例出现两个峰值,一个在变态前,另一个在变态后。从电子显微照片测量轴突直径表明,变态前髓鞘形成的临界直径为0.3微米,变态后为0.5微米。数据表明,视神经轴突的髓鞘形成有一个双相序列,第一阶段是变态前,第二阶段是变态后。第一阶段始于视神经孔,然后向眼球和视交叉两个方向延伸并持续到变态高峰期。在第二阶段,髓鞘形成始于视交叉,向眼球扩散,并且仅在最成熟的成年蛙中完成。第一阶段髓鞘形成的临界直径小于第二阶段。