Killander D, Lindahl P, Lundin L, Leary P, Gresser I
Eur J Immunol. 1976 Jan;6(1):56-9. doi: 10.1002/eji.1830060112.
We have determined the cell cycle position of individual mouse leukemia L 1210 cells by cytophotometric and autoradiographic techniques and simultaneously determined the amount of histocompatibility antigens expressed on the surface of individual cells by quantitative immunofluorescence. Interferon treatment of L 1210 cells was accompanied by an enhanced expression of histocompatibility surface antigens. The distribution of interferon-treated cells in the various phases of the cell cycle was similar to that for control cells and the enhanced expression of histocompatibility antigens was observed on interferon-treated cells in all phases of the cell cycle. We conclude, therefore, that this enhancement is not due to a preferential concentration of these cells in any one particular phase of the cell cycle.
我们通过细胞光度测定法和放射自显影技术确定了单个小鼠白血病L 1210细胞的细胞周期位置,同时通过定量免疫荧光法确定了单个细胞表面表达的组织相容性抗原的量。用干扰素处理L 1210细胞会伴随着组织相容性表面抗原表达的增强。经干扰素处理的细胞在细胞周期各阶段的分布与对照细胞相似,并且在细胞周期的所有阶段,经干扰素处理的细胞上均观察到组织相容性抗原表达增强。因此,我们得出结论,这种增强并非由于这些细胞在细胞周期的任何一个特定阶段的优先富集所致。