Kambayashi T, Michaëlsson J, Fahlén L, Chambers B J, Sentman C L, Kärre K, Ljunggren H G
Microbiology and Tumor Biology Center, Karolinska Institute, Stockholm, Sweden.
Eur J Immunol. 2001 Mar;31(3):869-75. doi: 10.1002/1521-4141(200103)31:3<869::aid-immu869>3.0.co;2-a.
Natural killer cells have been shown to interact with MHC class I molecules via inhibitory receptors. However, it is not known whether the inhibition induced by MHC class I molecules requires other NK cell-target cell interactions. Thus, we examined whether purified MHC class I molecules alone were able to inhibit NK cell function. Purified H-2K(b) and H-2D(b) molecules inhibited the release of IFN-gamma from spleen (H-2(b))-derived lymphokine-activated killer (LAK) cell cultures stimulated by anti-NK1.1 antibody in a concentration-dependent manner. LAK cells generated from newborn mice that express low levels of MHC class I binding Ly49 inhibitory receptors were significantly less sensitive to inhibition by H-2K(b) compared to LAK cells from adult mice. Furthermore, LAK cells generated from spleen cells of Ly49C-transgenic mice were significantly more sensitive to inhibition by H-2K(b) compared to non-transgenic littermates. Taken together, the data indicate that MHC class I induced inhibition of NK cell mediated effector functions, as assessed by IFN-gamma release after NK1.1 triggering, does not require additional cell surface molecules other than MHC class I.
自然杀伤细胞已被证明可通过抑制性受体与MHC I类分子相互作用。然而,尚不清楚MHC I类分子诱导的抑制作用是否需要其他自然杀伤细胞与靶细胞的相互作用。因此,我们研究了单独的纯化MHC I类分子是否能够抑制自然杀伤细胞功能。纯化的H-2K(b)和H-2D(b)分子以浓度依赖的方式抑制抗NK1.1抗体刺激的脾(H-2(b))来源的淋巴因子激活的杀伤(LAK)细胞培养物中IFN-γ的释放。与成年小鼠的LAK细胞相比,由表达低水平MHC I类结合Ly49抑制性受体的新生小鼠产生的LAK细胞对H-2K(b)抑制的敏感性明显较低。此外,与非转基因同窝小鼠相比,由Ly49C转基因小鼠的脾细胞产生的LAK细胞对H-2K(b)抑制的敏感性明显更高。综上所述,数据表明,如通过NK1.1触发后IFN-γ释放评估的那样,MHC I类诱导的对自然杀伤细胞介导的效应功能的抑制作用,除了MHC I类之外不需要其他细胞表面分子。