Steinberg M L, Defendi V
Proc Natl Acad Sci U S A. 1979 Feb;76(2):801-5. doi: 10.1073/pnas.76.2.801.
Human epidermal keratinocytes were infected by simian virus 40 in vitro. The structure of the developing keratinocyte colony reflects the spatial separation of cell division and keratinization in intact skin; thymidine-incorporating cells were primarily localized at the colony periphery whereas nondividing, histologically differentiated cells accumulated in the interior. Viral infection produced a dramatic increase in the size of the proliferative population as, simultaneously, differentiation was reduced in the colony interior. These changes were manifest when simian virus 40 T-antigen synthesis was detectable in only a small percentage of the cells; differentiation became increasingly density dependent as the percentage of T-antigen-positive cells rose over serial passage. The disruption of the normal pattern of growth/differentiation localization coincided with a loss of dependence on serum for growth, but preceded the appearance of other virus-induced properties associated with transformation; i.e., the ability to form colonies in soft agar and independence of growth from fibroblasts.
人表皮角质形成细胞在体外被猿猴病毒40感染。正在发育的角质形成细胞集落的结构反映了完整皮肤中细胞分裂和角质化的空间分离;掺入胸腺嘧啶核苷的细胞主要位于集落周边,而不进行分裂的、组织学上已分化的细胞则聚集在集落内部。病毒感染使增殖群体的大小显著增加,同时集落内部的分化减少。当仅在一小部分细胞中可检测到猿猴病毒40 T抗原合成时,这些变化就很明显了;随着T抗原阳性细胞百分比在连续传代中上升,分化变得越来越依赖密度。生长/分化定位的正常模式被破坏与对血清生长依赖性的丧失同时发生,但先于与转化相关的其他病毒诱导特性的出现;即,在软琼脂中形成集落的能力以及生长不依赖成纤维细胞。