Inoué S, Leblond C P, Laurie G W
J Cell Biol. 1983 Nov;97(5 Pt 1):1524-37. doi: 10.1083/jcb.97.5.1524.
The ultrastructure of Reichert's membrane, a thick basement membrane in the parietal wall of the yolk sac, has been examined in 13-14-d pregnant rats. This membrane is composed of more or less distinct parallel layers, each one of which resembles a common basement membrane. After routine fixation in glutaraldehyde followed by osmium tetroxide, the layers appear to be mainly composed of 3-8-nm thick cords arranged in a three-dimensional network. Loosely scattered among the cords are unbranched, straight tubular structures with a diameter of 7-10 nm, which mainly run parallel to the surface and to one another; they are referred to as basotubules. Permanganate fixation emphasizes the presence of a thick feltwork of irregular material around basotubules. Finally, minute dot-like structures measuring 3.5 nm and referred to as double pegs are present within the meshes of the cord network. Reichert's membranes have been treated for 2-48 h at 25 degrees C with plasmin, a proteolytic enzyme known to rapidly digest laminin and fibronectin. After a 2-h treatment, most of the substance of the cords is digested away leaving a three-dimensional network of 1.5-2.0-nm thick filaments. The interpretation is that the cords are formed of a plasmin-resistant core filament and a plasmin-extractable sheath. When plasmin treatment is prolonged for 15 h or longer, the filaments are dissociated and disappear, while basotubules are maintained. Plasmin digestion also reveals that basotubules are composed of two parts: a ribbon-like helical wrapping and tubule proper. Further changes in the tubule under plasmin influence are interpreted as a dissociation into pentagonal units suggestive of the presence of the amyloid P component. After 48 h of plasmin treatment, basotubules are further disaggregated and dispersed, leaving only linearly arranged double pegs. Reichert's membranes with or without a 2-hr plasmin treatment have been immunostained by exposure to antibodies against either laminin or type IV collagen with the help of peroxidase markers. The results indicate that the sheath of the cords contains laminin antigenicity, while the core filament contains type IV collagen antigenicity. It is proposed that Reichert's membrane consists mainly of a three-dimensional network of cords composed of a type IV collagen filament enclosed within a laminin-containing sheath. Also present are basotubules--which may contain the amyloid P component--and double pegs whose nature is unknown.
对妊娠13 - 14天大鼠卵黄囊壁中一层厚厚的基底膜——赖歇特膜的超微结构进行了研究。该膜由或多或少明显的平行层组成,每一层都类似于普通的基底膜。在经戊二醛常规固定后再用四氧化锇处理后,这些层似乎主要由排列成三维网络的3 - 8纳米厚的条索组成。在这些条索中松散分布着直径为7 - 10纳米的无分支直管状结构,它们主要与表面平行且相互平行;这些结构被称为基底小管。过锰酸盐固定突出了基底小管周围不规则物质的厚毡状网络的存在。最后,在条索网络的网眼中存在着直径为3.5纳米、被称为双钉的微小点状结构。赖歇特膜在25℃下用纤溶酶处理2 - 48小时,纤溶酶是一种已知能快速消化层粘连蛋白和纤连蛋白的蛋白水解酶。经过2小时处理后,大部分条索物质被消化掉,留下一个由1.5 - 2.0纳米厚的细丝组成的三维网络。由此推断,条索由抗纤溶酶的核心细丝和可被纤溶酶提取的鞘组成。当纤溶酶处理延长至15小时或更长时间时,细丝解离并消失,而基底小管则保留下来。纤溶酶消化还显示基底小管由两部分组成:一个带状螺旋包裹物和小管本身。在纤溶酶影响下小管的进一步变化被解释为解离成五边形单位,提示存在淀粉样蛋白P成分。经过48小时的纤溶酶处理后,基底小管进一步解体并分散,仅留下线性排列的双钉。用抗层粘连蛋白或IV型胶原抗体借助过氧化物酶标记对经或未经2小时纤溶酶处理的赖歇特膜进行免疫染色。结果表明,条索的鞘含有层粘连蛋白抗原性,而核心细丝含有IV型胶原抗原性。有人提出,赖歇特膜主要由由IV型胶原细丝包裹在含层粘连蛋白的鞘内组成的条索三维网络构成。还存在可能含有淀粉样蛋白P成分的基底小管以及性质未知的双钉。