Nature Communications · 2019 · 321 citations · 52 references
Life SciencesCell BiologyImmunologyCellular ImmunologyInnate ImmunityTranscriptomicsImmune Cell DifferentiationInnate Immune Cell DevelopmentNatural Killer Cell BiologyNatural Killer Cell DevelopmentSingle-cell Rna Sequencing AnalysisSingle-cell TranscriptomicsCell Death AssaysImmediate Early GenesNatural Killer Cell PrecursorsNatural Killer Cell ProgenitorsNatural Killer Cell Subset SpecificationPeripheral Blood Natural Killer CellsSingle-cell Rna SequencingTranscriptome Analysis
Abstract Natural killer (NK) cells are critical to both innate and adaptive immunity. However, the development and heterogeneity of human NK cells are yet to be fully defined. Using single-cell RNA-sequencing technology, here we identify distinct NK populations in human bone marrow and blood, including one population expressing higher levels of immediate early genes indicative of a homeostatic activation. Functionally matured NK cells with high expression of CX3CR1 , HAVCR2 (TIM-3), and ZEB2 represents terminally differentiated status with the unique transcriptional profile. Transcriptomic and pseudotime analyses identify a transitional population between CD56 bright and CD56 dim NK cells. Finally, a donor with GATA2 T354M mutation exhibits reduced percentage of CD56 bright NK cells with altered transcriptome and elevated cell death. These data expand our understanding of the heterogeneity and development of human NK cells.
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