Allen T D, Aplin J D, Campbell S
Department of Ultrastructure, Paterson Institute for Cancer Research, Christie Hospital, Manchester, U.K.
Scanning Microsc. 1988 Dec;2(4):2067-76.
Tissue interfaces such as basal lamina have been traditionally investigated in transmission electron microscopy by sections cut vertical to the lamina, presenting information restricted to a single ultrathin plane. In order to overcome this limitation, a methodology for surface visualisation of the underside cell membranes of the amniotic epithelium, the upper and lower basal lamina surfaces, and their relationship to the stromal collagen has been devised. This involves alkaline, detergent or enzymatic loosening and/or removal of the epithelial monolayer prior to fixation, followed by dry fracture after critical point drying. In this way we have visualised large areas of all interfaces and the inter-relationships between these elements during the process of stromal collagen production by the amniotic epithelial cells.
诸如基膜之类的组织界面传统上是在透射电子显微镜下通过垂直于基膜切割的切片进行研究的,所呈现的信息仅限于单个超薄平面。为了克服这一局限性,已设计出一种用于可视化羊膜上皮细胞底面细胞膜、上下基膜表面及其与基质胶原蛋白关系的方法。这包括在固定前通过碱性、去污剂或酶法使上皮单层松散和/或去除,然后在临界点干燥后进行干断裂。通过这种方式,我们在羊膜上皮细胞产生基质胶原蛋白的过程中可视化了所有界面的大片区域以及这些元素之间的相互关系。