Unit of Clinical and Experimental Immunology, Humanitas Clinical and Research Center, Milan, Italy.
Department of Medical Biotechnologies and Translational Medicine (BioMeTra), University of Milan, Milan, Italy.
Front Immunol. 2019 Aug 2;10:1812. doi: 10.3389/fimmu.2019.01812. eCollection 2019.
Natural Killer (NK) cells are innate lymphocytes playing pivotal roles in host defense and immune-surveillance. The homeostatic modulation of germ-line encoded/non-rearranged activating and inhibitory NK cell receptors (NKRs) determines the capability of these innate lymphocytes to either spare "self" cells or to kill viral-infected, tumor-transformed and heterologous cell targets. However, despite being discovered more than 40 years ago, several aspects of NK cell biology remain unknown or are still being debated. In particular, our knowledge of human NK cell ontogenesis and differentiation is still in its infancy as the majority of our experimental evidence on this topic mainly comes from findings obtained or with animal models . Although both the generation and the maintenance of human NK cells are sustained by hematopoietic stem cells (HSCs), the precise site(s) of NK cell development are still poorly defined. Indeed, HSCs and hematopoietic precursors are localized in different anatomical compartments that also change their ontogenic commitments before and after birth as well as in aging. Currently, the main site of NK cell generation and maturation in adulthood is considered the bone marrow, where their interactions with stromal cells, cytokines, growth factors, and other soluble molecules support and drive maturation. Different sequential stages of NK cell development have been identified on the basis of the differential expression of specific markers and NKRs as well as on the acquisition of specific effector-functions. All these phenotypic and functional features are key in inducing and regulating homing, activation and tissue-residency of NK cells in different human anatomic sites, where different homeostatic mechanisms ensure a perfect balance between immune tolerance and immune-surveillance. The present review summarizes our current knowledge on human NK cell ontogenesis and on the related pathways orchestrating a proper maturation, functions, and distributions.
自然杀伤 (NK) 细胞是先天淋巴细胞,在宿主防御和免疫监视中发挥关键作用。胚系编码/未重排的激活和抑制性 NK 细胞受体 (NKR) 的稳态调节决定了这些先天淋巴细胞是豁免“自身”细胞,还是杀伤病毒感染、肿瘤转化和异源细胞靶标。然而,尽管 NK 细胞被发现已经超过 40 年,但 NK 细胞生物学的几个方面仍然未知或仍存在争议。特别是,我们对人类 NK 细胞发生和分化的认识仍然处于起步阶段,因为我们关于这个主题的大部分实验证据主要来自在动物模型中获得的发现。尽管人类 NK 细胞的产生和维持都依赖于造血干细胞 (HSCs),但 NK 细胞发育的确切部位仍未定义。事实上,HSCs 和造血前体位于不同的解剖部位,这些部位在出生前后以及衰老过程中都会改变其发育承诺。目前,成年期 NK 细胞生成和成熟的主要部位被认为是骨髓,其中它们与基质细胞、细胞因子、生长因子和其他可溶性分子的相互作用支持并驱动成熟。基于特定标记物和 NKR 的差异表达以及特定效应功能的获得,已经确定了 NK 细胞发育的不同顺序阶段。所有这些表型和功能特征对于诱导和调节 NK 细胞在不同人体解剖部位的归巢、激活和组织驻留至关重要,在这些部位,不同的稳态机制确保了免疫耐受和免疫监视之间的完美平衡。本综述总结了我们目前对人类 NK 细胞发生以及协调适当成熟、功能和分布的相关途径的认识。