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胎鼠肝脏类器官培养(高密度培养)中肝细胞的形态、分化及基质产生

Morphology, differentiation and matrix production of liver cells in organoid cultures (high density cultures) of fetal rat livers.

作者信息

Elkasaby A, Xu D, Schröter-Kermani C, Merker H J

机构信息

Institut für Toxikologie und Embryonal-Pharmakologie, Freie Universität Berlin, FRG.

出版信息

Histol Histopathol. 1991 Apr;6(2):217-28.

PMID:1802120
Abstract

The aim of this study was to demonstrate the morphology and matrix synthesis of embryonic rat liver cells (day 18 of gestation) in organoid cultures (high density cultures) with electron microscopic and immunomorphological techniques. For this purpose the cells of embryonic rat livers were isolated enzymatically and grown in an organoid culture (high density culture) for 3 weeks in a Trowell system. During the first 48 h a sorting-out process took place, i.e. liver and blood-forming cells met to form aggregates. In between mesenchymal cells were seen. Vessel-like cavities developed. Electron microscopic inspection of the hepatocytes did not reveal any lesions of the cell organelles after 14 days in culture. As late as after a 3-week culture period mitochondrial swellings and an increased number of autophagic vacuoles were observed. A rim of collagenous fibrils or fibrillar bundles and granular matrix structures was perceptible as early as after 7 days in culture. Immunofluorescence microscopic techniques revealed collagen types III, IV and VI as well as laminin, nidogen, heparansulfate-proteoglycan and fibronectin in these areas. Thus, the composition of the matrix in this culture system corresponds (apart from the absence of collagen type I) to the embryonic situation. Therefore, the organoid culture appears to be an appropriate technique to study the behaviour of hepatocytes in vitro. It is especially suited to demonstrate the formation of matrix components in liver cells and their extracellular occurrence.

摘要

本研究的目的是运用电子显微镜和免疫形态学技术,展示类器官培养(高密度培养)中妊娠18天的胚胎大鼠肝细胞的形态和基质合成。为此,采用酶解法分离胚胎大鼠肝脏细胞,并在Trowell系统中进行类器官培养(高密度培养)3周。在最初的48小时内发生了细胞分选过程,即肝细胞和造血细胞聚集在一起。其间可见间充质细胞,类血管腔形成。培养14天后,对肝细胞进行电子显微镜检查未发现细胞器有任何损伤。直到培养3周后,才观察到线粒体肿胀和自噬空泡数量增加。早在培养7天后就能观察到胶原纤维或纤维束以及颗粒状基质结构形成的边缘。免疫荧光显微镜技术显示这些区域存在III型、IV型和VI型胶原以及层粘连蛋白、巢蛋白、硫酸乙酰肝素蛋白聚糖和纤连蛋白。因此,除了缺乏I型胶原外,该培养系统中基质的组成与胚胎期的情况相符。所以,类器官培养似乎是一种研究体外肝细胞行为的合适技术。它特别适合展示肝细胞中基质成分的形成及其在细胞外的存在情况。

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