Bernardini Giovanni, Antonangeli Fabrizio, Bonanni Valentina, Santoni Angela
Department of Molecular Medicine, Sapienza University, Rome, Italy; IRCCS NEUROMED - Mediterranean Neurological Institute, Isernia, Italy.
Department of Molecular Medicine, Sapienza University , Rome , Italy.
Front Immunol. 2016 Oct 6;7:402. doi: 10.3389/fimmu.2016.00402. eCollection 2016.
Chemokines are small chemotactic molecules that play key roles in physiological and pathological conditions. Upon signaling their specific receptors, chemokines regulate tissue mobilization and trafficking of a wide array of immune cells, including natural killer (NK) cells. Current research is focused on analyzing changes in chemokine/chemokine receptor expression during various diseases to interfere with pathological trafficking of cells or to recruit selected cell types to specific tissues. NK cells are a heterogeneous lymphocyte population comprising several subsets endowed with distinct functional properties and mainly representing distinct stages of a linear development process. Because of their different functional potential, the type of subset that accumulates in a tissue drives the final outcome of NK cell-regulated immune response, leading to either protection or pathology. Correspondingly, chemokine receptors, including CXCR4, CXCR3, and CXCR1, are differentially expressed by NK cell subsets, and their expression levels can be modulated during NK cell activation. At first, this review will summarize the current knowledge on the contribution of chemokines to the localization and generation of NK cell subsets in homeostasis. How an inappropriate chemotactic response can lead to pathology and how chemokine targeting can therapeutically affect tissue recruitment/localization of distinct NK cell subsets will also be discussed.
趋化因子是一类小的趋化分子,在生理和病理状态中发挥关键作用。在向其特定受体发出信号后,趋化因子调节多种免疫细胞的组织动员和运输,包括自然杀伤(NK)细胞。当前的研究集中于分析各种疾病期间趋化因子/趋化因子受体表达的变化,以干扰细胞的病理运输或招募特定类型的细胞至特定组织。NK细胞是一类异质性淋巴细胞群体,由几个具有不同功能特性的亚群组成,主要代表线性发育过程的不同阶段。由于其不同的功能潜力,在组织中积累的亚群类型决定了NK细胞调节的免疫反应的最终结果,导致保护或病理状态。相应地,趋化因子受体,包括CXCR4、CXCR3和CXCR1,在NK细胞亚群中差异表达,并且其表达水平在NK细胞激活过程中可被调节。首先,本综述将总结目前关于趋化因子在稳态下对NK细胞亚群的定位和产生所做贡献的认识。还将讨论不适当的趋化反应如何导致病理状态以及趋化因子靶向如何在治疗上影响不同NK细胞亚群的组织募集/定位。