McLoon S C, McLoon L K, Palm S L, Furcht L T
Department of Cell Biology and Neuroanatomy, University of Minnesota, Minneapolis 55455.
J Neurosci. 1988 Jun;8(6):1981-90. doi: 10.1523/JNEUROSCI.08-06-01981.1988.
The optic nerve of the developing rat was examined for the presence of laminin, an adhesive glycoprotein, to assess whether it might serve as a substrate for retinal axon growth in vivo. The optic stalk and nerve of developing rats were screened immunohistochemically for the presence of laminin before, during, and after the period of retinal axon growth. On embryonic day 14 (E14), laminin immunoreactivity was present in the ventral portion of the optic stalk, the same region in which the first retinal axons grow. Between E16 and postnatal day 10 (P10), cells positive for laminin were distributed throughout the cross-sectional area of the nerve. There was a progressive appearance of glial fibrillary acidic protein (GFAP) immunoreactivity, a marker for astrocytes, from the optic nerve head towards the chiasm beginning on E20. At the advancing front of GFAP immunoreactivity, cells were positive for both laminin and GFAP. Behind the front, laminin immunoreactivity disappeared from the cells. By P12, the only laminin immunoreactivity that remained within the optic nerve surrounded the vasculature. This is a time after the last retinal axons grow through the optic nerve. Monolayer cell cultures were prepared from perinatal rat optic nerves and processed for immunohistochemistry to determine which astrocyte type was laminin-positive. Type 1 astrocytes, which primarily compose the immature nerve, are GFAP-positive, A2B5-negative, and laminin-positive. Type 2 astrocytes, a major component of the mature optic nerve, were GFAP-positive, A2B5-positive and laminin-negative. An extract of developing optic nerve was analyzed by immunoblot along with laminin purified from Engelbreth-Holm-Swarm (EHS) sarcoma. Purified laminin ran with SDS-PAGE under reducing conditions as 2 bands with Mrs of 200,000 and 4000,000. Both bands reacted with antibodies to laminin. A low-salt extraction of whole optic nerve from E18 rats resulted in 2 bands with the same Mr as seen with laminin from EHS sarcoma. When only the inside of the optic nerve (which lacked the basal lamina and meninges that surround the outside) was processed, there was a dark 200,000 D band, but the 400,000 D band was virtually absent. These results are consistent with the hypothesis that laminin, or a variant form of laminin, serves as a substrate for retinal axon growth in the developing rat optic nerve.
为了评估层粘连蛋白(一种粘附性糖蛋白)是否可能在体内作为视网膜轴突生长的底物,研究人员对发育中大鼠的视神经进行了检查,以确定其中是否存在层粘连蛋白。在视网膜轴突生长期间及前后,通过免疫组织化学方法对发育中大鼠的视柄和视神经进行筛查,以检测层粘连蛋白的存在情况。在胚胎第14天(E14),层粘连蛋白免疫反应性出现在视柄的腹侧部分,即第一批视网膜轴突生长的同一区域。在E16至出生后第10天(P10)之间,层粘连蛋白阳性细胞分布在神经的整个横截面积内。从E20开始,从视神经乳头向视交叉方向,胶质纤维酸性蛋白(GFAP)免疫反应性逐渐出现,GFAP是星形胶质细胞的标志物。在GFAP免疫反应性的前沿,细胞同时对层粘连蛋白和GFAP呈阳性。在前沿之后,层粘连蛋白免疫反应性从细胞中消失。到P12时,视神经内仅存的层粘连蛋白免疫反应性围绕着血管系统。这是最后一批视网膜轴突穿过视神经之后的时间。从围产期大鼠视神经制备单层细胞培养物,并进行免疫组织化学处理,以确定哪种星形胶质细胞类型是层粘连蛋白阳性的。主要构成未成熟神经的1型星形胶质细胞是GFAP阳性、A2B5阴性且层粘连蛋白阳性。作为成熟视神经主要成分的2型星形胶质细胞是GFAP阳性、A2B5阳性且层粘连蛋白阴性。用从Engelbreth-Holm-Swarm(EHS)肉瘤中纯化的层粘连蛋白对发育中视神经的提取物进行免疫印迹分析。纯化的层粘连蛋白在还原条件下经SDS-PAGE电泳显示为两条带,分子量分别为200,000和400,000。两条带均与抗层粘连蛋白抗体发生反应。对E18大鼠的整个视神经进行低盐提取,得到两条与EHS肉瘤中层粘连蛋白分子量相同的带。当仅处理视神经内部(缺乏围绕外部的基膜和脑膜)时,出现一条深色的200,000 D带,但400,000 D带几乎不存在。这些结果与层粘连蛋白或其变体形式在发育中大鼠视神经中作为视网膜轴突生长底物的假设一致。