转录组
生物
人口
骨髓
自然杀伤细胞
细胞
先天免疫系统
细胞生物学
免疫学
单细胞分析
NK-92
白细胞介素21
基因
基因表达
遗传学
免疫系统
细胞毒性T细胞
T细胞
医学
环境卫生
体外
作者
Chao Yang,Jason Siebert,Robert Burns,Zachary J. Gerbec,Benedetta Bonacci,Amy L. Rymaszewski,Mary Rau,Matthew J. Riese,Sridhar Rao,Karen-Sue Carlson,John M. Routes,James Verbsky,Monica S. Thakar,Subramaniam Malarkannan
标识
DOI:10.1038/s41467-019-11947-7
摘要
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 CD56bright and CD56dim NK cells. Finally, a donor with GATA2T354M mutation exhibits reduced percentage of CD56bright 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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