INSERM, UMR-1160, Institut de Recherche St-Louis (IRSL), Paris, France.
Université Paris Diderot, Sorbonne Paris Cité, Paris, France.
Immunol Cell Biol. 2020 May;98(5):358-368. doi: 10.1111/imcb.12322. Epub 2020 Mar 18.
Almost 20 years ago, CD1d tetramers were developed to track invariant natural killer T (NKT) cells based on their specificity, and to define developmental steps during which differentiation markers and functional features are progressively acquired from early NKT cell precursor to fully mature NKT cell subsets. Based on these findings, a linear developmental model was proposed and subsequently used by all studies investigating the specific role of factors that control NKT cell development. More recently, based on intracellular staining patterns of lineage-specific transcription factors such as T-bet, GATA-3, promyelocytic leukemia zinc finger and RORγt, a lineage differentiation model was proposed for NKT cell development. Currently, studies on NKT cells development present lineage differentiation model data in addition to the linear maturation model. In the perspective presented here, we discuss current knowledge relating to NKT cell developmental models and particularly focus on the approaches and strategies, some of which appear nebulous, used to define NKT cell developmental stages and subsets.
大约 20 年前,基于其特异性,CD1d 四聚体被开发用于追踪不变自然杀伤 T(NKT)细胞,并定义在从早期 NKT 细胞前体到完全成熟的 NKT 细胞亚群的过程中,分化标志物和功能特征是如何逐步获得的。基于这些发现,提出了一个线性发育模型,并随后被所有研究 NKT 细胞发育特定控制因素的研究使用。最近,基于谱系特异性转录因子(如 T-bet、GATA-3、早幼粒细胞白血病锌指和 RORγt)的细胞内染色模式,提出了 NKT 细胞发育的谱系分化模型。目前,NKT 细胞发育的研究除了线性成熟模型外,还呈现了谱系分化模型数据。在本文中,我们讨论了与 NKT 细胞发育模型相关的最新知识,并特别关注用于定义 NKT 细胞发育阶段和亚群的方法和策略,其中一些方法和策略似乎还不太明确。