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2B4 (CD244)-CD48 interactions provide a novel MHC class I-independent system for NK-cell self-tolerance in mice

机译:2B4(CD244)-CD48相互作用为小鼠的NK细胞自我耐受提供了一种新的MHC I类独立系统

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摘要

Natural killer (NK) cells must be able to eliminate infected and transformed cells while remaining tolerant of normal cells. NK-cell self-tolerance is thought to be maintained by self-major histocompatibility complex (MHC) class I recognition; however, there are examples where NK cells are not regulated by MHC class I and yet remain self-tolerant. Here, we show that 2B4 (CD244) and CD48 represent a second system for murine NK-cell self-recognition. 2B4 and MHC class I receptors act nonredundantly to inhibit NK lysis of syngeneic tumor cells. NK cells from β2 microglobulin (β2m)-deficient mice and NK cells that lack expression of self-MHC-binding inhibitory receptors are inhibited by 2B4. Moreover, we provide the first in vivo evidence for MHC-independent NK self-recognition in a bone marrow rejection assay. These data suggest that NK-cell self-tolerance can be mediated by molecules other than MHC. (Blood. 2005;106:1337-1340)
机译:天然杀伤(NK)细胞必须能够消除感染和转化的细胞,同时仍能耐受正常细胞。 NK细胞的自我耐受被认为通过自我主要组织相容性复合体(MHC)I类识别来维持;但是,在某些例子中,NK细胞不受MHC I类调节,但仍具有自我耐受性。在这里,我们显示2B4(CD244)和CD48代表鼠NK细胞自我识别的第二个系统。 2B4和MHC I类受体非冗余地抑制同基因肿瘤细胞的NK裂解。 β2微球蛋白(β2m)缺陷小鼠的NK细胞和缺乏自身MHC结合抑制受体表达的NK细胞被2B4抑制。此外,我们提供了骨髓排斥试验中MHC非依赖性NK自我识别的第一个体内证据。这些数据表明,NK细胞的自我耐受性可以由MHC以外的分子介导。 (2005年; 106:1337-1340)

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