Stier H, Schlosshauer B
Naturwissenschaftliches und Medizinisches Institut, Reutlingen, Germany.
Glia. 1999 Jan 15;25(2):143-53. doi: 10.1002/(sici)1098-1136(19990115)25:2<143::aid-glia5>3.0.co;2-z.
Inhibition of incorrect axonal outgrowth has been shown to be a crucial guidance mechanism during the development of the nervous system. Within the visual system of chick and rat, extension of retinal ganglion cell axons is essentially restricted to distinct layers of the retina and distinct brain regions such as the tectum opticum. In addition, populations of ganglion cells from defined retina locations project topographically to defined tectal areas, their growth possibly being inhibited by radial glia in incorrect tectal regions. In the current study, we aimed to analyse potential inhibitory activity of retinal glia during outgrowth of ganglion cell axons of embryonic chick and rat. The response of ganglion cell axons originating from different retina locations when exposed to purified retinal radial glia cell membranes were monitored in collapse assays by time lapse video recording. The interaction of axons growing on purified glial somata or glial endfeet was analysed in outgrowth assays. Our results indicate that (1) nasal and temporal chick growth cones are equally induced to collapse by cell membranes from retinal radial glia: 75% nasal and 72% temporal. (2) The collapse inducing component of radial glia can be inactivated by defined heat treatment, reducing collapsing activity to 6% nasal and 5% temporal. (3) Rat growth cones respond in a similar way to chick radial glia. (4) Rat axons grow perfectly on endfeet but not on somata of radial glia of the chick. In summary, the data suggest that radial glia are functionally polarized with permissive endfeet and inhibitory somata based on heat-labile proteins. Glia polarization is likely to inhibit aberrant growth of ganglion cell axons into outer retina layers. However, retinal radial glia are unlikely to participate in preordering axons within the retina and therefore do not affect the topographic projection. Finally, the inhibitory function of radial glia is conserved between birds and mammals and represents possibly a fundamental mechanism for structuring the central nervous system.
在神经系统发育过程中,抑制错误的轴突生长已被证明是一种关键的导向机制。在鸡和大鼠的视觉系统中,视网膜神经节细胞轴突的延伸基本上局限于视网膜的特定层和特定的脑区,如视顶盖。此外,来自视网膜特定位置的神经节细胞群体按拓扑结构投射到视顶盖的特定区域,其生长可能受到错误视顶盖区域放射状胶质细胞的抑制。在本研究中,我们旨在分析胚胎期鸡和大鼠神经节细胞轴突生长过程中视网膜胶质细胞的潜在抑制活性。通过延时视频记录在塌陷试验中监测来自不同视网膜位置的神经节细胞轴突暴露于纯化的视网膜放射状胶质细胞膜时的反应。在生长试验中分析了在纯化的胶质细胞胞体或胶质细胞终足上生长的轴突之间的相互作用。我们的结果表明:(1)来自视网膜放射状胶质细胞的细胞膜能同样诱导鸡鼻侧和颞侧生长锥塌陷:鼻侧为75%,颞侧为72%。(2)放射状胶质细胞的塌陷诱导成分可通过特定的热处理失活,使塌陷活性降至鼻侧6%、颞侧5%。(3)大鼠生长锥对鸡放射状胶质细胞的反应方式相似。(4)大鼠轴突在鸡放射状胶质细胞的终足上生长良好,但在胞体上则不然。总之,数据表明放射状胶质细胞在功能上是极化的,基于热不稳定蛋白,其终足具有允许作用,胞体具有抑制作用。胶质细胞极化可能抑制神经节细胞轴突向视网膜外层的异常生长。然而,视网膜放射状胶质细胞不太可能参与视网膜内轴突的预排序,因此不影响拓扑投射。最后,放射状胶质细胞的抑制功能在鸟类和哺乳动物之间是保守的,可能代表了构建中枢神经系统的一种基本机制。