de Landazuri M O, López-Botet M, Timonen T, Ortaldo J R, Herberman R B
J Immunol. 1981 Oct;127(4):1380-3.
Human natural killer (NK) cells against K-562 tumor cells have been morphologically identified as large granular lymphocytes (LGL). We have investigated whether LGL are also responsible for NK activity against a variety of adherent and nonadherent tumor cell lines. LGL-enriched fractions, obtained by centrifugation of nonadherent mononuclear cells on discontinuous density gradients of Percoll, contained high levels of spontaneous and interferon- (IFN) boosted NK activity against each of the target cells tested. In contrast, the LGL-depleted functions, which contain most of the typical small lymphocytes, were devoid of NK activity and did not develop appreciable activity after treatment with IFN. The ability of the different fractions to exert NK activity correlated with their capacity to form conjugates with nonadherent tumor cells. Reconstitution of the different fractions with macrophages did not increase the NK activity of already cytotoxic fractions and did not induce appreciable activity in the LGL-depleted fractions. On the other hand, mixtures of highly cytotoxic and nonreactive cell fractions did not reveal the presence of suppressor cells for NK in the nonreactive fractions. Taken together, our data demonstrate that both spontaneous and IFN-boosted NK activity is confined to the LGL-enriched fractions and suggest that LGL are the main effector cells exerting NK cytotoxicity against a variety of adherent as well as nonadherent tumor cell lines.
人类自然杀伤(NK)细胞对K - 562肿瘤细胞在形态上已被鉴定为大颗粒淋巴细胞(LGL)。我们研究了LGL是否也负责对多种贴壁和非贴壁肿瘤细胞系的NK活性。通过在不连续的Percoll密度梯度上离心非贴壁单核细胞获得的富含LGL的组分,对每种测试的靶细胞都具有高水平的自发和干扰素(IFN)增强的NK活性。相比之下,富含大多数典型小淋巴细胞的去除LGL的组分没有NK活性,并且在用IFN处理后也没有产生明显的活性。不同组分发挥NK活性的能力与其与非贴壁肿瘤细胞形成共轭物的能力相关。用巨噬细胞重建不同组分并没有增加已经具有细胞毒性的组分的NK活性,也没有在去除LGL的组分中诱导出明显的活性。另一方面,高细胞毒性和无反应性细胞组分的混合物并没有揭示无反应性组分中存在NK抑制细胞。综上所述,我们的数据表明,自发和IFN增强的NK活性都局限于富含LGL的组分,并表明LGL是对多种贴壁和非贴壁肿瘤细胞系发挥NK细胞毒性的主要效应细胞。