| Literature DB >> 33945787 |
Adelle P McFarland1, Adam Yalin2, Shuang-Yin Wang2, Victor S Cortez1, Tomer Landsberger2, Raki Sudan1, Vincent Peng1, Hannah L Miller1, Biancamaria Ricci1, Eyal David2, Roberta Faccio3, Ido Amit4, Marco Colonna5.
Abstract
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.Entities:
Keywords: EOMES; HOBIT; TCF-1; glycolysis; innate lymphoid cells; natural killer cells; single-cell RNA sequencing; tissue; transcription factor; tumor
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Year: 2021 PMID: 33945787 PMCID: PMC8312473 DOI: 10.1016/j.immuni.2021.03.024
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 43.474