Murata E, Zimmermann B, Merker H J, Akita M, Kaneko K
Institute of Toxicology and Prenatal Pharmacology, Free University of Berlin, Germany.
Acta Anat (Basel). 1995;153(2):96-105. doi: 10.1159/000147719.
Basement membrane formation of fetal mouse intestinal epithelial cells was investigated in organoid cultures. Intestinal cells were dissociated with a commercial collagenase/dispase preparation, and the cells were grown at high density on a membrane filter at the interface between the medium and air. This type of culture allows the histotypical reorganization of cells. After 2 days in culture, epithelial cells began to accumulate on the surface, in particular the periphery of the culture. These cells were usually cuboid, and small vesicles were formed in the center of the culture. Laminin-positive material was observed at peripheral sites. However, no basement membrane could be identified beneath the epithelial cells at the electron-microscopic level. After 3 days, epithelial cells that had gathered at the periphery became columnar in shape. Laminin-positive material extended across the surface of the culture. However, the vesicles formed in the center of the culture were not associated with laminin-positive material. Basement membrane was observed by electron microscopy at some sites beneath groups of epithelial cells, but did not extend continuously beneath these cells. Some epithelial cells made contact with the underlying mesenchymal cells through the discontinuous basement membrane via intercellular contacts. After 5-6 days, the surface of the culture was almost completely covered with epithelial cells and, at some sites, villus-like structures were visible. Laminin-positive material was clearly detectable under epithelial cells, as well as around epithelial vesicles located in the center of the culture. By electron microscopy, basement membrane was clearly visible between the epithelial and mesenchymal cells. After 9 days, villus-like structures were rarely observed. After 3 weeks, the cell mass had become smaller and villi had disappeared. Basement membrane was extensively folded and no basement membrane was visible at some sites. Formation of basement membrane by epithelial cells in monolayer culture occurs in an incomplete and irregular manner. It occurs rapidly in organoid cultures that include mesenchyme and epithelium. The organoid culture used here should be a useful tool for studies of the formation and degeneration of the basement membrane as well as interactions between the epithelium and mesenchyme.
在类器官培养中研究了胎鼠肠上皮细胞的基底膜形成。用市售的胶原酶/分散酶制剂解离肠细胞,然后将细胞在培养基与空气界面的膜滤器上高密度培养。这种培养方式可使细胞进行组织学重排。培养2天后,上皮细胞开始在表面尤其是培养物周边积聚。这些细胞通常呈立方形,培养物中央形成小泡。在周边部位观察到层粘连蛋白阳性物质。然而,在电子显微镜下上皮细胞下方未发现基底膜。3天后,聚集在周边的上皮细胞变为柱状。层粘连蛋白阳性物质延伸至培养物表面。然而,培养物中央形成的小泡与层粘连蛋白阳性物质无关。在一些上皮细胞群下方的部位通过电子显微镜观察到基底膜,但在这些细胞下方并未连续延伸。一些上皮细胞通过不连续的基底膜经细胞间接触与下方的间充质细胞接触。5 - 6天后,培养物表面几乎完全被上皮细胞覆盖,在一些部位可见绒毛样结构。在上皮细胞下方以及培养物中央的上皮小泡周围均可清晰检测到层粘连蛋白阳性物质。通过电子显微镜观察,上皮细胞和间充质细胞之间可见清晰的基底膜。9天后,很少观察到绒毛样结构。3周后,细胞团变小,绒毛消失。基底膜广泛折叠,在一些部位未见基底膜。单层培养中上皮细胞形成基底膜的过程不完整且不规则。在包含间充质和上皮的类器官培养中基底膜形成迅速。此处使用的类器官培养应是研究基底膜形成与退化以及上皮与间充质之间相互作用的有用工具。