Vanselow J, Thanos S, Godement P, Henke-Fahle S, Bonhoeffer F
Max-Planck-Institut für Entwicklungsbiologie, Tübingen, F.R.G.
Brain Res Dev Brain Res. 1989 Jan 1;45(1):15-27. doi: 10.1016/0165-3806(89)90003-5.
Neuroanatomical tracing of retinal axons and axonal terminals with the fluorescent dye, DiI, was combined with immunohistochemical characterization of radial glial cells in the developing chick retinotectal system. Emphasis was placed on the mode of the tectal innervation by individual retinal axons and on the distribution and fate of the tectal radial glial cells and their spatial relation to retinal axons. It was obvious from fluorescent images obtained from anterogradely filled axons that these axons deserted the superficial stratum opticum (SO) to penetrate the stratum griseum et fibrosum superficiale (SGFS) by making right-angled turns within the SO. Frequently, axons which had invaded the SGFS were bifurcated and had a superficial branch which remained within the SO. Terminal axonal arborization occurred at various depths within the SGFS. Characterization of the tectal glial cells and their radial fibers by means of the anti-filament antibody, R5, and post-mortem staining with the fluorescent dye, DiI, revealed the following. (a) At least from day E8 to P1, tectal glial fibers traversed all tectal layers from the periventricular location of their somata to the superficial interface between SO and pia mater. In this interface they enlarged and formed characteristic endfeet. (b) Glial endfeet covered the whole tectal surface. They showed at early ages anterior-posterior differences having a higher density in the posterior tectum. These differences disappeared at embryonic day E13. (c) After innervation, glial endfeet of the anterior tectal third were arranged in rows parallel to the retinal fibers within the SO. This arrangement was not observed in eyeless embryos. (d) Radial glial fibers could be stained with R5 from day E8 to late embryonic stages throughout their entire length. (e) At the first posthatching days, only the segments of the radial glial fibers restricted to the thickness of the SO were R5-positive, although the fibers still traversed throughout the depth of the tectum. The results are discussed in context to the genesis of the retinotectal projection.
利用荧光染料DiI对视网膜轴突和轴突终末进行神经解剖追踪,并结合对发育中的鸡视网膜顶盖系统中放射状胶质细胞的免疫组织化学特征分析。研究重点在于单个视网膜轴突对顶盖的支配方式,以及顶盖放射状胶质细胞的分布、命运及其与视网膜轴突的空间关系。从顺行填充轴突获得的荧光图像可以明显看出,这些轴突离开浅表层视神经(SO),在SO内直角转弯,穿透浅灰质和纤维质层(SGFS)。侵入SGFS的轴突经常分叉,并有一个留在SO内的浅表分支。轴突终末分支发生在SGFS内的不同深度。通过抗丝抗体R5对顶盖胶质细胞及其放射状纤维进行表征,并使用荧光染料DiI进行死后染色,结果如下:(a)至少从胚胎第8天到出生后第1天,顶盖胶质纤维从其胞体的脑室周围位置穿过所有顶盖层,到达SO与软脑膜之间的浅表界面。在这个界面处,它们膨大并形成特征性的终足。(b)胶质终足覆盖整个顶盖表面。在早期,它们显示出前后差异,后顶盖的密度更高。这些差异在胚胎第13天消失。(c)神经支配后,顶盖前三分之一的胶质终足在SO内与视网膜纤维平行排列。在无眼胚胎中未观察到这种排列。(d)从胚胎第8天到胚胎后期,放射状胶质纤维全长都能用R5染色。(e)在孵化后的头几天,尽管放射状胶质纤维仍贯穿顶盖深度,但只有局限于SO厚度的部分是R5阳性。结合视网膜顶盖投射的发生过程对这些结果进行了讨论。