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单层培养中肝细胞质膜的分化

Differentiation of the plasma membrane of hepatic cells in monolayer cultures.

作者信息

Perissel B, Charbonné F, Chessebeuf M, Malet P

出版信息

Cell Tissue Res. 1976 Aug 20;171(2):157-73. doi: 10.1007/BF00219404.

Abstract

Hepatocytes from rats were isolated by treatment with trypsin and cultured. Plasma membranes at different culture stages were observed by electron microscopy. The activities of 5' nucleotidase and adenosinetriphosphatase on the plasma membranes were examined. The cell coat was also studied by use of the concanavalin A-peroxidase technique. The surfaces of single cells, covered with microvilli, are the site of adenosinetriphosphatase activity only and are devoid of 5'-nucleotidase activity. After a few h of culture, the cells are grouped together in tight clusters or long trails and are separated by an intercellular space of 250 A, partially permeable to lanthanum nitrate. The juxtaposed plasma membranes on which 5'-nucleotidase and adenosinetriphosphatase activities occur also delimit spaces similar to bile canaliculi. The formation of junction complexes and their permeability to lanthanum nitrate was also studied. No enzymatic activity is observed at the junctions. The numerous tight junctions, impervious to the tracer, are always accompanied by a profusion of microfilaments. Mature desmosomes are rare, and are present only in the form of "maculae adhaerentes diminutae." The gap junctions, nearly always permeable to the tracer, form rapidly and assume a variety of shapes (trail, bulge and ring-like), the significance of which is open to discussion. The use of concanavalin A permits localization of the free sugar sites on the surface of the cells, in the pinocytotic vesicles and in the internal space of the gap junctions.

摘要

用胰蛋白酶处理大鼠肝细胞并进行培养。通过电子显微镜观察不同培养阶段的质膜。检测质膜上5'-核苷酸酶和三磷酸腺苷酶的活性。还利用伴刀豆球蛋白A-过氧化物酶技术研究了细胞被膜。单个细胞表面覆盖着微绒毛,是仅存在三磷酸腺苷酶活性的部位,不存在5'-核苷酸酶活性。培养数小时后,细胞紧密聚集在一起形成紧密的团块或长链,细胞间有250埃的间隙,对硝酸镧部分通透。并列的质膜上同时存在5'-核苷酸酶和三磷酸腺苷酶活性,也界定了类似于胆小管的间隙。还研究了连接复合体的形成及其对硝酸镧的通透性。连接处未观察到酶活性。众多对示踪剂不透的紧密连接总是伴有大量微丝。成熟的桥粒很少见,仅以“微小粘着斑”的形式存在。间隙连接几乎总是对示踪剂通透,形成迅速且呈现多种形状(链状、凸起状和环状),其意义有待探讨。使用伴刀豆球蛋白A可定位细胞表面、胞饮小泡和间隙连接内部空间中的游离糖位点。

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