Vitolo D, Vujanovic N L, Rabinowich H, Schlesinger M, Herberman R B, Whiteside T L
Department of Pathology, University of Pittsburgh, School of Medicine, PA.
J Immunol. 1993 Aug 15;151(4):1926-37.
Natural killer (NK) cells selected by IL-2-induced rapid adherence to plastic and called A-NK cells represent a phenotypically and functionally distinct subset of mature peripheral blood NK cells. To further characterize this subset of NK cells functionally, their potential to express mRNA for the IL-2R and various cytokines after IL-2 activation was examined. Highly purified normal human peripheral blood resting NK (R-NK) cells were obtained by negative immunoselection using OKT3 mAb and magnetic beads coated with goat anti-mouse Ig. By two-color flow cytometry, > 90% of these R-NK cells were either CD3-CD56+CD16+ or - or CD3-CD56-CD16+. R-NK cells were activated in the presence of 6000 IU/ml (22 nM) of IL-2 for different periods of time. After 1, 3, 5, or 24 h, plastic-adherent (A) and nonadherent (NA) NK cells were separated and compared for the expression of the IL-2R or cytokine mRNA by in situ hybridization, using 35[S]-cDNA probes. Only low proportions of R-NK cells expressed genes for IL-2Rp55 (16%) or cytokines IL-2 (20%), IFN-gamma (18%), TNF-alpha (16%), and TGF-beta (7%). Thus, the genes for the IL-2Rp55 and these cytokines were not constitutively expressed by most human R-NK cells, and there was no indication that the NK cells used in these experiments were activated in vivo or during the purification procedure. However, larger proportions of R-NK cells showed expression of mRNA for IL-1-beta (35%) and IL-6 (40%), which indicates that genes for these cytokines may be constitutively expressed in a substantial proportion of normal human circulating NK cells. When R-NK cells were incubated in the presence of 22 nM of IL-2 for 1 to 24 h and separated into A-NK cells and NA-NK cells, a large proportion of A-NK cells became positive for IL-2R and cytokine gene expression. In contrast, the proportion of mRNA-positive NA-NK cells was similar or lower than that observed for R-NK cells, with the exception of an increase in TGF-beta.(ABSTRACT TRUNCATED AT 400 WORDS)
通过白细胞介素-2诱导快速黏附于塑料培养板而筛选出的自然杀伤(NK)细胞,称为A-NK细胞,它代表了成熟外周血NK细胞中一个表型和功能都不同的亚群。为了进一步从功能上对这一NK细胞亚群进行特性描述,研究了其在白细胞介素-2激活后表达白细胞介素-2受体(IL-2R)和各种细胞因子mRNA的潜力。使用OKT3单克隆抗体和包被有山羊抗小鼠Ig的磁珠,通过阴性免疫筛选获得高度纯化的正常人外周血静息NK(R-NK)细胞。通过双色流式细胞术检测,这些R-NK细胞中>90%为CD3-CD56+CD16+或CD3-CD56-CD16+。R-NK细胞在6000 IU/ml(22 nM)白细胞介素-2存在的情况下激活不同时间。在1、3、5或24小时后,分离塑料黏附(A)和非黏附(NA)NK细胞,使用35[S]-cDNA探针通过原位杂交比较IL-2R或细胞因子mRNA的表达。只有低比例的R-NK细胞表达IL-2Rp55基因(16%)或细胞因子白细胞介素-2(20%)、干扰素-γ(18%)、肿瘤坏死因子-α(16%)和转化生长因子-β(7%)。因此,大多数人R-NK细胞不组成性表达IL-2Rp55基因和这些细胞因子基因,并且没有迹象表明这些实验中使用的NK细胞在体内或纯化过程中被激活。然而,较大比例的R-NK细胞显示白细胞介素-1-β(35%)和白细胞介素-6(40%)mRNA的表达,这表明这些细胞因子基因可能在相当比例的正常人循环NK细胞中组成性表达。当R-NK细胞在22 nM白细胞介素-2存在的情况下孵育1至24小时并分离为A-NK细胞和NA-NK细胞时,很大比例的A-NK细胞IL-2R和细胞因子基因表达呈阳性。相反,mRNA阳性的NA-NK细胞比例与R-NK细胞相似或更低,但转化生长因子-β有所增加。(摘要截选至400字)