Lehman J M, Laffin J, Jacobberger J W, Fogleman D
Department of Microbiology and Immunology, Albany Medical College, New York 12208.
Cytometry. 1988 Jan;9(1):52-9. doi: 10.1002/cyto.990090109.
Quantitative two-color fluorescent analysis of Simian virus (SV40) infection of permissive CV-1 cells was investigated. Analysis included by quantitation of cellular DNA, the early viral tumor (T) antigen with a monoclonal antibody, and late viral (V) antigens with a polyclonal antibody. T antigen was detected in all phases of the cell cycle at 6 and 12 h, after SV40 infection of growth arrested cells. At later time intervals, the percentage of T-antigen-positive cells increased with the induction of the cells into successive rounds of DNA synthesis and an increase in tetraploid-polyploid cells. The amount of T antigen per cell increased as the cells entered the successive stages of the cell cycle (G0/G1----G2 + M----tetraploid S and G2 + M). The V antigen from adsorbed virus was detected immediately after infection. Synthesis of V antigen began in late S and G2 + M phases of the cell cycle. This quantitative analysis allows a definitive determination of antigen per cell in a population correlated with the cell cycle and may be useful in correlating viral and cellular events with transformation.
对允许性CV - 1细胞感染猿猴病毒(SV40)进行了定量双色荧光分析。分析包括对细胞DNA进行定量,用单克隆抗体检测早期病毒肿瘤(T)抗原,以及用多克隆抗体检测晚期病毒(V)抗原。在生长停滞细胞被SV40感染后6小时和12小时,在细胞周期的所有阶段都检测到了T抗原。在随后的时间间隔里,随着细胞被诱导进入连续的DNA合成轮次以及四倍体 - 多倍体细胞数量增加,T抗原阳性细胞的百分比也增加。随着细胞进入细胞周期的连续阶段(G0/G1----G2 + M----四倍体S期和G2 + M期),每个细胞中T抗原的量增加。感染后立即检测到来自吸附病毒的V抗原。V抗原的合成始于细胞周期的S期末期和G2 + M期。这种定量分析能够明确确定群体中每个细胞的抗原数量,并与细胞周期相关,可能有助于将病毒和细胞事件与转化联系起来。