Naramura M, Hu R J, Gu H
Laboratory of Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, Maryland 20852, USA.
Immunity. 1998 Aug;9(2):209-16. doi: 10.1016/s1074-7613(00)80603-2.
Production of interleukin (IL)-2 by T lymphocytes is one of the earliest events during immune response. A mutant mouse strain was generated by replacing the IL-2 gene with a cDNA encoding green fluorescent protein (GFP). In this model, GFP fluorescence is readily detectable upon T cell activation and is mostly coexpressed with IL-2 at the single cell level. Thus, individual activated T cells can express the IL-2 gene biallelically. Upon stimulation through the T cell antigen receptor, CD4+ cells separate into distinct GFP+ and GFP- populations, both of which are capable of differentiating into either Th1 or Th2 effectors. These mice allow noninvasive detection of IL-2 production by single cells and analysis of the subsequent differentiative fate of these cells as an immune response develops.
T淋巴细胞产生白细胞介素(IL)-2是免疫反应中最早发生的事件之一。通过用编码绿色荧光蛋白(GFP)的cDNA替换IL-2基因,培育出了一种突变小鼠品系。在该模型中,T细胞激活后很容易检测到GFP荧光,并且在单细胞水平上GFP大多与IL-2共表达。因此,单个活化的T细胞可以双等位基因表达IL-2基因。通过T细胞抗原受体刺激后,CD4 +细胞分为不同的GFP +和GFP-群体,这两个群体都能够分化为Th1或Th2效应细胞。这些小鼠能够对单细胞产生的IL-2进行非侵入性检测,并在免疫反应发展过程中分析这些细胞随后的分化命运。