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对整合膜糖蛋白细胞表面表达具有温度条件性的中国仓鼠卵巢细胞系的分离。

Isolation of Chinese hamster ovary cell lines temperature conditional for the cell-surface expression of integral membrane glycoproteins.

作者信息

Hearing J, Hunter E, Rodgers L, Gething M J, Sambrook J

机构信息

Department of Microbiology, State University of New York, Stony Brook 11794.

出版信息

J Cell Biol. 1989 Feb;108(2):339-53. doi: 10.1083/jcb.108.2.339.

Abstract

A procedure is described to select mutants of Chinese hamster ovary cells that are conditionally defective for the cell-surface expression of integral membrane glycoproteins, including the hemagglutinin (HA) of influenza virus. Using a combination of cell sorting and biochemical screening, seven cell lines were obtained that express more cell-surface HA at 32 degrees C than at 39 degrees C. The production of infectious vesicular stomatitis virus, whose growth requires insertion of an integral membrane protein into the plasma membrane, was also temperature conditional in the majority of these mutant cell lines. Five of the lines synthesized apparently normally core-glycosylated HA at the elevated temperature but the protein was neither displayed on the cell surface nor accumulated intracellularly. In these cell lines, little or no terminally glycosylated HA molecules were observed after synthesis at 39 degrees C. By contrast, the core glycosylation of HA and several other integral membrane proteins was abnormal in the remaining two cell lines at both permissive and restrictive temperatures, due to a lesion in a cellular gene(s) that affects the formation of and/or the addition of mannose-rich oligosaccharide chains to newly synthesized polypeptides. Although HA was transported to the plasma membrane at both 32 and 39 degrees C, it did not accumulate on the cell surface at the higher temperature, apparently because of an increased rate of degradation.

摘要

本文描述了一种筛选中国仓鼠卵巢细胞突变体的方法,这些突变体在整合膜糖蛋白(包括流感病毒血凝素(HA))的细胞表面表达方面存在条件性缺陷。通过结合细胞分选和生化筛选,获得了7个细胞系,这些细胞系在32℃时比在39℃时表达更多的细胞表面HA。大多数这些突变细胞系中,生长需要将整合膜蛋白插入质膜的传染性水疱性口炎病毒的产生也受温度条件影响。其中5个细胞系在高温下合成的核心糖基化HA明显正常,但该蛋白既未显示在细胞表面,也未在细胞内积累。在这些细胞系中,39℃合成后几乎观察不到或没有末端糖基化的HA分子。相比之下,在其余两个细胞系中,在允许温度和限制温度下,HA和其他几种整合膜蛋白的核心糖基化均异常,这是由于一个细胞基因发生损伤,影响了新合成多肽上富含甘露糖的寡糖链的形成和/或添加。尽管HA在32℃和39℃时都被转运到质膜,但在较高温度下它并未在细胞表面积累,显然是因为降解速率增加。

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