Reichenbach A, Schneider H, Leibnitz L, Reichelt W, Schaaf P, Schümann R
Carl Ludwig Institute of Physiology, Leipzig, German Democratic Republic.
Anat Embryol (Berl). 1989;180(1):71-9. doi: 10.1007/BF00321902.
Radial glial (Müller) cells of the rabbit retina were studied by various techniques including Golgi impregnation, scanning electron microscopy, horseradish peroxidase application, and staining of enzymatically isolated cells. This combination of methods produced detailed information on the specialized morphology of the Müller cells within the different topographical regions of the retina, and of the Müller cell processes within the various retinal layers. As a general rule, the retinal periphery contains short thick Müller cells with big endfeet, whereas the thick central retina is occupied by long slender cells with small endfeet. Independent of their location within the retina, Müller cell processes were found to be adapted to the structure of the surrounding retinal layers. Within the outer and inner nuclear layers, Müller cell processes (and somata) extend thin cytoplasmic "bubbles" ensheathing the neuronal somata, as do the "velate" astrocytes in the brain. In the plexiform layers, Müller cells extend many fine side branches between the neuropil, comparable to the protoplasmic astrocytes of the brain. In the thick myelinated nerve fibre layer of the central retina the Müller cell processes are rather smooth, similar to those of fibrous astrocytes. It is concluded that the neuronal microenvironment determines the morphology of a given glial process, or even of a part of a glial process running through a specialized neuronal compartment.
通过多种技术对兔视网膜的放射状胶质(穆勒)细胞进行了研究,这些技术包括高尔基染色法、扫描电子显微镜、辣根过氧化物酶应用以及对酶解分离细胞的染色。这种方法组合产生了关于视网膜不同地形区域内穆勒细胞的特殊形态以及各视网膜层内穆勒细胞突起的详细信息。一般来说,视网膜周边区域含有短而粗且终足大的穆勒细胞,而视网膜中央厚层则被长而细且终足小的细胞占据。无论穆勒细胞在视网膜内的位置如何,都发现其突起与周围视网膜层的结构相适应。在外核层和内核层内,穆勒细胞突起(以及胞体)会伸出薄的细胞质“泡”包裹神经元胞体,就如同大脑中的“薄被”星形胶质细胞一样。在神经纤维层中,穆勒细胞在神经毡之间伸出许多细小的侧支,类似于大脑中的原浆性星形胶质细胞。在视网膜中央厚的有髓神经纤维层中,穆勒细胞突起相当平滑,类似于纤维性星形胶质细胞的突起。可以得出结论,神经元微环境决定了特定胶质细胞突起的形态,甚至决定了穿过特定神经元区域的胶质细胞突起部分的形态。