Comprehensive Cancer Center, The Ohio State University, Columbus, OH 43210.
Medical Scientist Training Program, Biomedical Sciences Graduate Program, The Ohio State University, Columbus, OH 43210.
J Immunol. 2020 Nov 15;205(10):2679-2693. doi: 10.4049/jimmunol.2000434. Epub 2020 Oct 5.
Human NK cells develop in tonsils through discrete NK cell developmental intermediates (NKDIs), yet the mechanistic regulation of this process is unclear. We demonstrate that Notch activation in human tonsil-derived stage 3 (CD34CD117CD94NKp80) and 4A (CD34CD117CD94NKp80) NKDIs promoted non-NK innate lymphoid cell differentiation at the expense of NK cell differentiation. In contrast, stage 4B (CD34CD117CD94NKp80) NKDIs were NK cell lineage committed despite Notch activation. Interestingly, whereas NK cell functional maturation from stage 3 and 4A NKDIs was independent of Notch activation, the latter was required for high NKp80 expression and a stage 4B-like phenotype by the NKDI-derived NK cells. The Notch-dependent effects required simultaneous engagement with OP9 stromal cells and were also stage-specific, with NOTCH1 and NOTCH2 receptors regulating stage 3 NKDIs and NOTCH1 primarily regulating stage 4A NKDIs. These data establish stage-specific and stromal-dependent roles for Notch in regulating human NK cell developmental plasticity and maturation.
人类自然杀伤 (NK) 细胞在扁桃体中通过离散的 NK 细胞发育中间态 (NKDIs) 发育,但这一过程的机制调节尚不清楚。我们证明,人扁桃体来源的阶段 3 (CD34CD117CD94NKp80) 和 4A (CD34CD117CD94NKp80) NKDIs 中的 Notch 激活促进了非 NK 固有淋巴细胞的分化,而牺牲了 NK 细胞的分化。相比之下,尽管 Notch 被激活,但阶段 4B (CD34CD117CD94NKp80) NKDIs 是 NK 细胞谱系定向的。有趣的是,尽管 Notch 激活对于从阶段 3 和 4A NKDIs 中获得 NK 细胞的功能成熟是可有可无的,但它对于 NKDI 衍生的 NK 细胞中高 NKp80 表达和类似 4B 阶段的表型是必需的。Notch 依赖性的影响需要与 OP9 基质细胞的同时结合,并且还具有阶段特异性,NOTCH1 和 NOTCH2 受体调节阶段 3 NKDIs,而 NOTCH1 主要调节阶段 4A NKDIs。这些数据确立了 Notch 在调节人类 NK 细胞发育可塑性和成熟中的阶段特异性和基质依赖性作用。