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DNA介导的基因转移后鼠成纤维细胞表达人单核细胞膜抗原gp55

Expression of the human monocyte membrane antigen gp55 by murine fibroblasts after DNA-mediated gene transfer.

作者信息

Ashmun R A, Peiper S C, Rebentisch M B, Look A T

出版信息

Blood. 1987 Mar;69(3):886-92.

PMID:3545322
Abstract

Human DNA sequences that contain the gene encoding gp55, a cell surface glycoprotein expressed exclusively on mature human monocytes and monocytic leukemia cells, were isolated in a mouse genetic background. DNA from mature human monocytes was cotransfected with DNA from a molecularly cloned feline sarcoma virus containing the v-fms oncogene into NIH-3T3 cells. Transformed mouse fibroblasts that expressed gp55, based on their reactivity with the MY4, B44.1, or LeuM3 monoclonal antibodies, were selected by fluorescence-activated cell sorting. Regardless of which antibody was used for selection, equivalent binding of all three antibodies was observed for positive transformants. Secondary and tertiary mouse cell transformants were obtained after additional rounds of transfection and cell sorting with the use of DNA from primary and then secondary transformants. Southern blot analysis of the cellular DNA from two independently derived tertiary subclones revealed a limited complement of human sequences, thus indicating that the gene encoding gp55 is included in fewer than 50 kilobases of human DNA. Independently derived tertiary subclones displayed concordant patterns of reactivity with 13 monocyte-specific monoclonal antibodies, thus indicating that each recognized an epitope on the product (gp55) of a single human gene. The 55-kilodalton cell surface polypeptide was specifically immunoprecipitated with a representative monoclonal antibody, 26if, from lysates of enzymatically radioiodinated peripheral blood monocytes and tertiary transformants. We conclude that gp55 is highly immunogenic and that a large number of independently derived monoclonal antibodies specific for human monocytes react with epitopes on this one molecule.

摘要

在小鼠遗传背景下分离出了包含编码gp55基因的人类DNA序列,gp55是一种仅在成熟人类单核细胞和单核细胞白血病细胞上表达的细胞表面糖蛋白。将来自成熟人类单核细胞的DNA与来自含有v-fms癌基因的分子克隆猫肉瘤病毒的DNA共转染到NIH-3T3细胞中。根据它们与MY4、B44.1或LeuM3单克隆抗体的反应性,通过荧光激活细胞分选选择表达gp55的转化小鼠成纤维细胞。无论使用哪种抗体进行选择,阳性转化体均观察到所有三种抗体的等效结合。在使用来自初级转化体然后是次级转化体的DNA进行额外轮次的转染和细胞分选后,获得了二级和三级小鼠细胞转化体。对来自两个独立衍生的三级亚克隆的细胞DNA进行Southern印迹分析,结果显示人类序列的互补片段有限,因此表明编码gp55的基因包含在少于50千碱基的人类DNA中。独立衍生的三级亚克隆与13种单核细胞特异性单克隆抗体显示出一致的反应模式,因此表明每种抗体都识别单个人类基因产物(gp55)上的一个表位。用代表性单克隆抗体26if从酶促放射性碘化外周血单核细胞和三级转化体的裂解物中特异性免疫沉淀出55千道尔顿的细胞表面多肽。我们得出结论,gp55具有高度免疫原性,并且大量针对人类单核细胞的独立衍生单克隆抗体与该单一分子上的表位发生反应。

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