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禽肿瘤病毒感染的鸡胚成纤维细胞中细胞表面抗原的超微结构分布

Ultrastructural distribution of cell surface antigens in avian tumor virus-infected chick embryo fibroblasts.

作者信息

Phillips E R, Perdue J F

出版信息

J Cell Biol. 1974 Jun;61(3):743-56. doi: 10.1083/jcb.61.3.743.

Abstract

The distribution of neoantigens in the surface membrane of avian tumor virus-infected chicken embryo fibroblasts was examined on carbon replicas of cell cultures using hemocyanin-labeled antibody. New determinants appearing on the cell surface of virally infected but not transformed cells are thought to be common with components of the viral envelope. These antigens were found to exist in a diffuse, random array on the dorsal cell surface, with a denser accumulation along the cell processes. In living cells, surface antigens are capable of several types of redistribution when activated by reaction with antibody. Leukosis virus-infected (non-transformed) cells showed two apparently independent modes of redistribution: a relocation of some antibody-related sites to the cell margin; or an involvement of essentially all sites in randomly dispersed aggregates. Viral antigenic sites on sarcoma virus-infected (transformed) cells, reacted with antibody, were able to produce weak marginal relocation; but revealed a more striking tendency to migrate to some central location. The centripetal coalescence thus formed resembles the "cap" noted in other systems. Prior aggregation into "patches" may not be a prerequisite for such cap formation. Tumor-specific surface antigen detection and mapping was attempted by this technique, but results were equivocal. An antigen possibly characteristic of rapidly dividing cells occurred in a sparse, diffuse fashion over the surface of morphologically distinct "round" cells.

摘要

利用血蓝蛋白标记的抗体,在细胞培养物的碳复型上检测禽肿瘤病毒感染的鸡胚成纤维细胞表面膜上新抗原的分布。病毒感染但未转化的细胞表面出现的新决定簇被认为与病毒包膜成分相同。这些抗原被发现以弥散、随机的阵列形式存在于细胞背表面,沿细胞突起处有更密集的聚集。在活细胞中,表面抗原在与抗体反应激活后能够进行几种类型的重新分布。白血病病毒感染(未转化)的细胞表现出两种明显独立的重新分布模式:一些与抗体相关的位点重新定位到细胞边缘;或者基本上所有位点参与随机分散的聚集体。肉瘤病毒感染(转化)的细胞上的病毒抗原位点与抗体反应后,能够产生微弱的边缘重新定位;但显示出更明显的向某个中心位置迁移的趋势。由此形成的向心聚结类似于在其他系统中观察到的“帽”。在这种帽形成之前聚集成“斑块”可能不是必需的。尝试用这种技术检测和定位肿瘤特异性表面抗原,但结果不明确。一种可能是快速分裂细胞特征性的抗原以稀疏、弥散的方式出现在形态上不同的“圆形”细胞表面。

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