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Isolation of Virus‐producing Transformants from Human Gastric Cancer Cell Line HGC‐27 Infected with Human T‐cell Leukemia Virus Type I

机译:从感染了I型人T细胞白血病病毒的人胃癌细胞株HGC-27中分离出产病毒的转化子

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摘要

A human anaplastic gastric cancer cell line, HGC‐27, showed marked degeneration with formation of multinucleated syncytia and cell detachment of nearly all cells which began 24 hr after and reached a maximum 2 to 3 days after co‐cultivation with X‐irradiated MT‐2 cells, HTLV‐I producing human cord leukocytes. Less severe degeneration without formation of syncytia was also observed in the cultures inoculated with cell‐free MT‐2 culture media. Morphologically altered cells began to proliferate and formed piled up colonies in some of the cultures co‐cultivated with X‐irradiated MT‐2 cells after a long culture period. The two clones designated HGC/MT2 (Cl‐1) and HGC/MT2 (Cl‐2) were separated by cell cloning. HGC/MT2 (Cl‐1) and HGC/MT2 (Cl‐2) cells were positive for HTLV‐I gag proteins (p19 and p24) and pX gene products, p40x, as demonstrated by immunohistochemistry and immunoblotting analysis, contained HTLV‐I provirus DNA, and consistently produced type C virus particles.
机译:人类间变性胃癌细胞HGC-27表现出明显的变性,形成多核合胞体,几乎所有细胞的细胞分离都开始于X射线MT-共培养24小时后,最长达到2至3天。 2个细胞,HTLV-I产生人脐带白细胞。在接种无细胞MT-2培养基的培养物中,未出现合胞体的严重变性也较少。经过长时间培养后,与X射线照射的MT-2细胞共同培养的某些培养物中,形态改变的细胞开始增殖并形成堆积的菌落。通过细胞克隆分离了命名为HGC / MT2(Cl-1)和HGC / MT2(Cl-2)的两个克隆。免疫组织化学证实,HGC / MT2(Cl-1)和HGC / MT2(Cl-2)细胞对HTLV-1 gag蛋白(p19和p24)和pX基因产物p40 x 呈阳性和免疫印迹分析,包含HTLV-I前病毒DNA,并始终产生C型病毒颗粒。

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