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源自表达杂交胰岛素基因-癌基因的转基因小鼠的β细胞系。

Beta-cell lines derived from transgenic mice expressing a hybrid insulin gene-oncogene.

作者信息

Efrat S, Linde S, Kofod H, Spector D, Delannoy M, Grant S, Hanahan D, Baekkeskov S

机构信息

Cold Spring Harbor Laboratory, NY 11724.

出版信息

Proc Natl Acad Sci U S A. 1988 Dec;85(23):9037-41. doi: 10.1073/pnas.85.23.9037.

Abstract

Three pancreatic beta-cell lines have been established from insulinomas derived from transgenic mice carrying a hybrid insulin-promoted simian virus 40 tumor antigen gene. The beta tumor cell (beta TC) lines maintain the features of differentiated beta cells for about 50 passages in culture. The cells produce both proinsulin I and II and efficiently process each into mature insulin, in a manner comparable to normal beta cells in isolated islets. Electron microscopy reveals typical beta-cell type secretory granules, in which insulin is stored. Insulin secretion is inducible up to 30-fold by glucose, although with a lower threshold for maximal stimulation than that for normal beta cells. beta TC lines can be repeatedly derived from primary beta-cell tumors that heritably arise in the transgenic mice. Thus, targeted expression of an oncogene with a cell-specific regulatory element can be used both to immortalize a rare cell type and to provide a selection for the maintenance of its differentiated phenotype.

摘要

已从携带杂交胰岛素启动的猿猴病毒40肿瘤抗原基因的转基因小鼠的胰岛素瘤中建立了三种胰腺β细胞系。β肿瘤细胞(βTC)系在培养中可维持约50代分化β细胞的特征。这些细胞产生胰岛素原I和II,并能以与分离胰岛中的正常β细胞相当的方式有效地将每种胰岛素原加工成成熟胰岛素。电子显微镜显示典型的β细胞型分泌颗粒,其中储存着胰岛素。葡萄糖可诱导胰岛素分泌增加达30倍,尽管最大刺激的阈值低于正常β细胞。βTC系可从转基因小鼠中遗传性出现的原发性β细胞肿瘤中反复获得。因此,利用细胞特异性调节元件靶向表达癌基因,既可以使一种罕见细胞类型永生化,又可以为维持其分化表型提供选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f8f/282658/887d0246a4b0/pnas00302-0277-a.jpg

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