先天性淋巴细胞
生物
脾脏
白细胞介素12
淋巴因子激活杀伤细胞
白细胞介素21
先天免疫系统
脂肪组织
细胞生物学
干扰素
免疫学
免疫系统
T细胞
细胞毒性T细胞
内分泌学
体外
生物化学
作者
Adelle P. McFarland,Adam Yalin,Shuang-Yin Wang,Victor S. Cortez,Tomer Landsberger,Raki Sudan,Vincent Peng,Hannah L. Miller,Biancamaria Ricci,Eyal David,Roberta Faccio,Ido Amit,Marco Colonna
出处
期刊:Immunity
[Elsevier]
日期:2021-06-01
卷期号:54 (6): 1320-1337.e4
被引量:89
标识
DOI:10.1016/j.immuni.2021.03.024
摘要
Natural killer (NK) cells and type 1 innate lymphoid cells (ILC1s) are heterogenous innate lymphocytes broadly defined in mice as Lin-NK1.1+NKp46+ cells that express the transcription factor T-BET and produce interferon-γ. The ILC1 definition primarily stems from studies on liver and small intestinal populations. However, NK1.1+NKp46+ cells in the salivary glands, uterus, adipose, and other tissues exhibit nonuniform programs that differ from those of liver or intestinal ILC1s or NK cells. Here, we performed single-cell RNA sequencing on murine NK1.1+NKp46+ cells from blood, spleen, various tissues, and solid tumors. We identified gene expression programs of tissue-specific ILC1s, tissue-specific NK cells, and non-tissue-specific populations in blood, spleen, and other tissues largely corresponding to circulating cells. Moreover, we found that circulating NK cell programs were reshaped in tumor-bearing mice. Core programs of circulating and tumor NK cells paralleled conserved human NK cells signatures, advancing our understanding of the human NK-ILC1 spectrum.
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