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Distinct Phenotypic and Functional Characteristics of Human Natural Killer Cells Obtained by Rapid Interleukin 2-Induced Adherence to Plastic

白细胞介素21 生物 自然杀伤细胞 白细胞介素2 CD49b K562细胞 Janus激酶3 分子生物学 淋巴因子激活杀伤细胞 白细胞介素15 免疫学 抗原 自然杀伤性T细胞 细胞生物学 白细胞介素12 表型 细胞毒性T细胞 CD16 体外 白细胞介素 细胞因子 CD8型 CD3型 生物化学 白血病
作者
Nikola L. Vujanović,Hannah Rabinowich,Young Jo Lee,L. Jost,Ronald B. Herberman,Theresa L. Whiteside
出处
期刊:Cellular Immunology [Elsevier]
卷期号:151 (1): 133-157 被引量:70
标识
DOI:10.1006/cimm.1993.1227
摘要

Human natural killer (NK) cells can be functionally subdivided into adherent (A) and nonadherent (NA) subpopulations. In the presence of 22 nM of interleukin 2(IL2), a substantial proportion of resting (R)-NK cells developed adherence to plastic as early as after 5 min of IL2 incubation, and by 1-5 hr of IL2 induction, 16% (range, 4-30%) of NK cells were adherent. Optimal concentration of IL2 for adherence of NK cells was 2-22 nM. This adherence was blocked completely by antibody to IL2 receptor (IL2R)-β and, partially, by antibodies to β1 or β2 integrins, ICAM-1, CD2 or LFA3, but not by antibodies to the IL2R-α or CD56 antigen. ANK cells separated from NA-NK cells after 5 hr of incubation in the presence of IL2 were significantly (P<0.05) enriched in CD56dimCD16dim or -IL2Rp55+ and IL2Rp75+ cells, but were depleted of CD56bright CD16- cells. While surface density of CD56 and CD16 antigens was lower, that of β2 integrins (CD18, CD11a, CD11b) was higher on A-NK than on NA-NK cells. In a single-cell cytotoxicity assay, 61% of A-NK vs 37% of NA-NK cells bound, and 24% of A-NK vs 11% of NA-NK cells killed, K562 targets. In 4-day cultures with 0.02 or 2.2 nM of IL2, A-NK cells developed lymphokine-activated killer (LAK) activity later than NA-NK cells. By autoradiography, three to eight times more A-NK than NA-NK cells incorporated [3H]TdR into cell nuclei between 48 and 96 hr of IL2 incubation. In 14-day cultures in the presence of 22 nM of IL2, A-NK cells, which were initially adherent but later grew as single-cell suspensions, proliferated better (30-fold; P<0.03) and expressed lower membrane density of CD56 than NA-NK cells. In culture, A-NK cells had consistently higher cytotoxicity against K562 targets than NA-NK cells, but cytotoxicity against Daudi was similar for both subsets. The data indicate that short incubation (1-5 hr) of human NK cells in the presence of 22 nM of IL2 allows for selection of a subpopulation which differs from the rest of NK cells not only by properties of rapid adherence to plastic, but also by a characteristic phenotype (CD3-CD56dim or- CD16dim or -β2integrinsbrightIL2Rp75+), rapid expression of IL2R-α, higher NK activity, delayed development of LAK activity, and ability to respond optimally in the presence of 22 nM of IL2. Thus, A-NK cells appear to be a phenotypically and functionally distinct subset of mature NK cells.

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