Gaze R M, Fawcett J W
J Embryol Exp Morphol. 1983 Feb;73:17-38.
We have used Horseradish peroxidase to investigate the pathways taken by Xenopus optic fibres regenerating from normal and electrophysiologically-confirmed compound eyes to the optic tectum. Optic fibres, when sectioned near the chiasma, regenerate up both sides of the diencephalon to both tecta. We have therefore been able, by using animals in which one eye had or had not been removed at early embryonic stages, to look at the behaviour of regenerating axons in three different situations: (1) regeneration to the contralateral tectum, previously innervated by the sectioned fibres; (2) regeneration to a "virgin' ipsilateral tectum, never before innervated by optic fibres; and (3) regeneration to an ipsilateral tectum already innervated by fibres from a normal eye. From the chiasma to the tectodiencephalic junction regenerating fibres behave similarly in all three situations, following roughly the course of the normal optic tract, but running in a rather disorganised way, with frequent crossing over of fibres. However fibres of nasal retinal origin (from an NN eye) spread to occupy a much larger area of the side of the diencephalon than those of temporal origin (from a TT eye). From the tectodiencephalic junction to the tectal termination of the fibres there are differences between the three situations investigated; fibres regenerating to a 'virgin' ipsilateral, or to a denervated contralateral tectum, tend to grow straight onto the tectum, instead of being channelled into lateral or medial brachium as uncut fibres tend to be. There is however, the remains of a brachial organisation, and of differential selection of these brachia by fibres from the different types of compound eye, this being well seen on "virgin' tecta. Fibres regenerating to an ipsilateral innervated tectum behave very differently. As they reach the tectodiencephalic junction they suddenly start to grow in a less disorganised way, and are channelled into well defined brachia. If from a compound eye, these fibres terminate on only that part of the tectum innervated by fibres from the corresponding part of the normal eye. Thus fibres from a VV eye and those from the ventral half of the normal eye all terminate on medial tectum; fibres from an NN eye, and those from the nasal half of the normal eye all terminate in caudal tectum; and temporal fibres from both normal and TT eyes terminate in rostral tectum.
我们利用辣根过氧化物酶来研究非洲爪蟾的视神经纤维从正常以及经电生理学确认的复眼再生至视顶盖所采用的路径。视神经纤维在视交叉附近被切断后,会向间脑两侧再生至两侧的视顶盖。因此,通过使用在胚胎早期阶段一只眼睛已被摘除或未被摘除的动物,我们得以观察在三种不同情况下再生轴突的行为:(1)再生至对侧视顶盖,该视顶盖先前由被切断的纤维所支配;(2)再生至“未被支配过的”同侧视顶盖,该视顶盖从未被视神经纤维支配过;(3)再生至已被来自正常眼睛的纤维支配的同侧视顶盖。从视交叉到视顶盖 - 间脑交界处,再生纤维在这三种情况下的表现相似,大致沿着正常视束的路径,但排列相当紊乱,纤维频繁交叉。然而,来自鼻侧视网膜(来自NN眼)的纤维比来自颞侧视网膜(来自TT眼)的纤维在间脑一侧占据更大的区域。从视顶盖 - 间脑交界处到纤维在视顶盖的终止部位,在所研究的三种情况之间存在差异;再生至“未被支配过的”同侧或去神经支配的对侧视顶盖的纤维,倾向于直接生长到视顶盖上,而不是像未被切断的纤维那样被引导进入外侧或内侧臂。然而,臂状组织的遗迹以及来自不同类型复眼的纤维对这些臂的差异选择仍然存在,这在“未被支配过的”视顶盖上清晰可见。再生至同侧已被支配的视顶盖的纤维表现则大不相同。当它们到达视顶盖 - 间脑交界处时,突然开始以一种不那么紊乱的方式生长,并被引导进入明确的臂中。如果来自复眼,这些纤维仅终止于视顶盖中由正常眼睛相应部分的纤维所支配的那部分。因此,来自VV眼的纤维以及来自正常眼睛腹侧半部分的纤维都终止于内侧视顶盖;来自NN眼的纤维以及来自正常眼睛鼻侧半部分的纤维都终止于尾侧视顶盖;来自正常眼睛和TT眼的颞侧纤维都终止于 Rostral 视顶盖。