Chan F L, Inoue S, Leblond C P
Department of Anatomy, McGill University, Montreal, Canada.
Cell Tissue Res. 1993 Jul;273(1):41-52. doi: 10.1007/BF00304610.
When tissues are processed for electron microscopy by conventional methods, such as glutaraldehyde fixation followed by rapid dehydration in acetone, basement membranes show two main layers: the electron-lucent "lamina lucida". (or rara) and the electron-dense "lamina densa". In an attempt to determine whether this subdivision is real or artefactual, two approaches have been used. Firstly, rat and mouse seminiferous tubules, mouse epididymis and associated tissues, and anterior parts of mouse eyes were subjected to cryofixation by instant freezing followed by freeze substitution in a -80 degrees C solution of osmium tetroxide in dry acetone, which was gradually warmed to room temperature over a 3-day period. The results indicate that, in areas devoid of ice crystals, basement membranes consist of a lamina densa in direct contact with the plasmalemma of the associated cells without an intervening lamina lucida. Secondly, a series of tissues from mice perfused with 3% glutaraldehyde were cryoprotected in 30% glycerol, frozen in Freon 22 and subjected to a 3-day freeze substitution in osmium tetroxide-acetone as above. Under these conditions, no lamina lucida accompanies the lamina densa in the basement membranes of the majority of tissues, including kidney, thyroid gland, smooth and skeletal muscle, ciliary body, seminiferous tubules, epididymis and capillary endothelium. Thus, even though these tissues have been fixed in glutaraldehyde, no lamina lucida appears when they are slowly dehydrated by freeze substitution. It is concluded that the occurrence of this lamina in conventionally processed tissues is not due to fixation but to the rapid dehydration. However, in this series of experiments, the basement membranes of trachea and plantar epidermis include a lamina lucida along their entire length, while those of esophagus and vas deferens may or may not include a lamina lucida. To find out if the lamina lucida appearing under these conditions is a real structure or an artefact, the trachea and epidermis were fixed in paraformaldehyde and slowly dehydrated by freeze substitution. Under these conditions, no lamina lucida was found. Since this result is the same as observed in other tissues by the previous approaches, it is proposed that the lamina lucida is an artefact in these as in the other investigated basement membranes. Thus, basement membranes are simply composed of a lamina densa that closely follows the plasmalemma of the associated cells.(ABSTRACT TRUNCATED AT 400 WORDS)
当用传统方法对组织进行电子显微镜检查时,比如先用戊二醛固定,然后在丙酮中快速脱水,基底膜会显示出两个主要层次:电子透明的“透明板”(或稀疏板)和电子致密的“致密板”。为了确定这种细分是真实存在的还是人为造成的,人们采用了两种方法。首先,对大鼠和小鼠的生精小管、小鼠附睾及相关组织,以及小鼠眼睛的前部进行冷冻固定,即瞬间冷冻,然后在-80℃的四氧化锇干丙酮溶液中进行冷冻置换,并在3天时间内逐渐升温至室温。结果表明,在没有冰晶的区域,基底膜由一层与相关细胞的质膜直接接触的致密板组成,中间没有透明板。其次,用3%戊二醛灌注小鼠后获取的一系列组织,在30%甘油中进行冷冻保护,在氟利昂22中冷冻,然后像上述那样在四氧化锇-丙酮中进行3天的冷冻置换。在这些条件下,包括肾脏、甲状腺、平滑肌和骨骼肌、睫状体、生精小管、附睾和毛细血管内皮在内的大多数组织的基底膜中,致密板都没有伴随透明板。因此,即使这些组织已用戊二醛固定,但通过冷冻置换缓慢脱水时,也不会出现透明板。得出的结论是,在传统处理的组织中出现这种透明板不是由于固定,而是由于快速脱水。然而,在这一系列实验中,气管和足底表皮的基底膜在其整个长度上都包括透明板,而食管和输精管的基底膜可能有也可能没有透明板。为了弄清楚在这些条件下出现的透明板是真实结构还是人为产物,将气管和表皮用多聚甲醛固定并通过冷冻置换缓慢脱水。在这些条件下,没有发现透明板。由于这个结果与之前在其他组织中观察到的结果相同,所以有人提出,在这些组织以及其他研究的基底膜中,透明板都是人为产物。因此,基底膜仅由一层紧密跟随相关细胞质膜的致密板组成。(摘要截取自400字)