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自然杀伤细胞上的识别结构。

Recognition structures on natural killer cells.

作者信息

Yokoyama W M

机构信息

Department of Medicine, Mount Sinai Medical Center, New York, New York 10029.

出版信息

Curr Opin Immunol. 1993 Feb;5(1):67-73. doi: 10.1016/0952-7915(93)90083-5.

Abstract

Recent studies have identified cell surface molecules that appear to play important roles in natural killer cell specificity for their targets. Natural killer cells display activation 'receptors', such as NKR-P1 molecules in rodents, that may activate cytotoxicity by transducing biochemical signals. These molecules presumably interact with target cell surface ligands but these structures have not been elucidated. Natural killer cells display other molecules, such as Ly-49 in mice, that appear to be 'inhibitory' receptors that engage target cell MHC class I molecules and deliver signals, negatively regulating natural killer cell cytotoxic activity. The murine NKR-P1 and Ly-49 molecules are structurally similar and encoded by members of polymorphic gene families that reside in the natural killer gene complex on the distal region of mouse chromosome 6. Additional molecules have been serologically defined and studied functionally in murine and human systems. Thus, the specificity of an individual natural killer cell may be determined by its expressed repertoire of these molecules. The complexities of this recognition system are beginning to be appreciated at the molecular level.

摘要

最近的研究已经确定了一些细胞表面分子,它们似乎在自然杀伤细胞对其靶标的特异性中发挥重要作用。自然杀伤细胞表达激活“受体”,如啮齿动物中的NKR-P1分子,这些受体可能通过转导生化信号来激活细胞毒性。这些分子可能与靶细胞表面配体相互作用,但这些结构尚未阐明。自然杀伤细胞还表达其他分子,如小鼠中的Ly-49,这些分子似乎是“抑制性”受体,它们与靶细胞的MHC I类分子结合并传递信号,从而负向调节自然杀伤细胞的细胞毒性活性。小鼠的NKR-P1和Ly-49分子在结构上相似,由位于小鼠6号染色体远端区域的自然杀伤基因复合体中的多态基因家族成员编码。在小鼠和人类系统中,已经通过血清学方法定义了其他分子并对其功能进行了研究。因此,单个自然杀伤细胞的特异性可能由其表达的这些分子的组合决定。这种识别系统的复杂性在分子水平上开始得到认识。

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