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自然杀伤细胞毒性因子在自然杀伤细胞杀伤靶细胞机制中的作用。

Role of natural killer cytotoxic factors in the mechanism of target-cell killing by natural killer cells.

作者信息

Bonavida B, Wright S C

出版信息

J Clin Immunol. 1986 Jan;6(1):1-8. doi: 10.1007/BF00915358.

Abstract

Studies on the mechanism of cell-mediated cytotoxicity (CMC) have suggested a stimulus-secretion model and implicated a role of soluble cytotoxic mediators. Our studies in the natural killer (NK) system provide several lines of evidence for the involvement of natural killer cytotoxic factors (NKCF) in NK CMC and led to the development of a model for the NK lytic mechanism. This model delineates several interactions between NK cells and targets that are deemed necessary to achieve target-cell lysis. The first stage is the interaction of the effector with the target cell, resulting in contact and adhesion. This is presumably mediated by NK recognition structures and target-cell structures. Following binding, the target cell stimulates the NK cell to release NKCF. This step is functionally distinct from the initial effector-target binding. The trigger mechanism for release of NKCF appears to be dependent on protein kinase C. The released NKCF binds to NKCF binding sites on the target cell followed by "processing" or "internalization" and, ultimately, resulting in cell death. This model has been shown to be useful in investigating the mechanism of defective NK activity in certain disease states. Biochemical analysis and comparative studies suggest that NKCF is a distinct molecule from other cytotoxins studied to date. The studies in the NK CMC system supporting a role of cytotoxic mediators also suggest a possible role for cytotoxic factors in other cytotoxic systems. Furthermore, the selective susceptibility to lysis of tumor or infected cells by NKCF suggests a possible role of their effectiveness in in vivo therapy.

摘要

对细胞介导的细胞毒性(CMC)机制的研究提出了一种刺激-分泌模型,并暗示了可溶性细胞毒性介质的作用。我们在自然杀伤(NK)系统中的研究为自然杀伤细胞毒性因子(NKCF)参与NK CMC提供了多条证据,并促成了一种NK裂解机制模型的建立。该模型描述了NK细胞与靶细胞之间的几种相互作用,这些相互作用被认为是实现靶细胞裂解所必需的。第一阶段是效应细胞与靶细胞的相互作用,导致接触和黏附。这大概是由NK识别结构和靶细胞结构介导的。结合后,靶细胞刺激NK细胞释放NKCF。这一步在功能上与最初的效应细胞-靶细胞结合不同。NKCF释放的触发机制似乎依赖于蛋白激酶C。释放的NKCF与靶细胞上的NKCF结合位点结合,随后进行“加工”或“内化”,最终导致细胞死亡。该模型已被证明在研究某些疾病状态下NK活性缺陷的机制方面是有用的。生化分析和比较研究表明,NKCF是一种与迄今研究的其他细胞毒素不同的分子。在NK CMC系统中支持细胞毒性介质作用的研究也表明细胞毒性因子在其他细胞毒性系统中可能发挥作用。此外,NKCF对肿瘤或感染细胞裂解的选择性敏感性表明它们在体内治疗中的有效性可能发挥作用。

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