Garcia-Peñarrubia Pilar, Lorenzo Nieves, Galvez Jesus, Campos Adolfo, Ferez Xavier, Rubio Gonzalo
Department of Biochemistry and Molecular Biology B and Immunology, School of Medicine, 30100 Espinardo, Murcia, Spain.
Cell Immunol. 2002 Feb;215(2):141-50. doi: 10.1016/s0008-8749(02)00023-0.
In earlier work, we established a mathematical model to characterize the binding properties of cytotoxic cells to target cells. These properties can be described by the values of the maximum effector and target conjugate frequencies, alpha(max) and beta(max), respectively, and the dissociation constant of the conjugates formed, K(D) (Garcia-Peñarrubia, P., Cabrera, L., Alvarez, R., and Galvez, J., J. Immunol. Methods 155 (1992) 133). Here, we address the problem of exploring the physical meaning of these parameters and their relationships with cytotoxicity. With this purpose, conjugation between a human leukemic NK cell line (NKL) and K562 tumor cells has been studied from binding isotherms obtained from data of effector (alpha) and target (beta) conjugate frequencies measured by flow cytometry analysis at different effector-to-target ratios (R). The results have been compared to those obtained after target cells treatment with monoclonal antibodies recognizing adhesion molecules ICAM-1 (CD54) and LFA-3 (CD58) (which are able to block some of the receptors implicated in conjugation), as well as with cholera toxin (CTX) that can modify the state of affinity of some adhesion molecules such as LFA-1 (CD11a/CD18). The results show that: (1) blocking adhesion receptors CD54 and CD58 on the surface of target cells leads to a significant decrease of alpha(max) and beta(max), indicating that these parameters are related to the density of expression of receptors implicated in effector-target adhesion; (2) treatment of effector cells with CTX induced an increase of K(D), demonstrating that this parameter is associated with the effector-target affinity of the system; and (3) parallel experiments of conjugation and cytotoxicity showed that effector-target affinity and saturability influence the cytotoxic activity of the effector population.
在早期的研究中,我们建立了一个数学模型来描述细胞毒性细胞与靶细胞的结合特性。这些特性可以分别用最大效应细胞与靶细胞结合频率值α(max)和β(max)以及形成的结合物的解离常数K(D)来描述(Garcia-Peñarrubia, P., Cabrera, L., Alvarez, R., and Galvez, J., J. Immunol. Methods 155 (1992) 133)。在此,我们探讨这些参数的物理意义及其与细胞毒性的关系。为此,我们通过流式细胞术分析在不同效应细胞与靶细胞比例(R)下测量的效应细胞(α)和靶细胞(β)结合频率数据得到的结合等温线,研究了人白血病NK细胞系(NKL)与K562肿瘤细胞之间的结合。将结果与用识别黏附分子ICAM-1(CD54)和LFA-3(CD58)的单克隆抗体处理靶细胞后得到的结果进行了比较(这些抗体能够阻断一些参与结合的受体),同时也与能够改变一些黏附分子如LFA-1(CD11a/CD18)亲和力状态的霍乱毒素(CTX)处理后的结果进行了比较。结果表明:(1)阻断靶细胞表面的黏附受体CD54和CD58会导致α(max)和β(max)显著降低,表明这些参数与参与效应细胞 - 靶细胞黏附的受体表达密度有关;(2)用CTX处理效应细胞会导致K(D)增加,表明该参数与系统的效应细胞 - 靶细胞亲和力有关;(3)结合和细胞毒性的平行实验表明,效应细胞 - 靶细胞亲和力和饱和性会影响效应细胞群体的细胞毒性活性。