Genetic distinction between functional tissue-resident and conventional natural killer cells

被引:3
|
作者
Hu, Luni [1 ]
Han, Mengwei [1 ]
Deng, Yichen [1 ]
Gong, Jingjing [2 ]
Hou, Zhiyuan [2 ]
Zeng, Yanyu [1 ]
Zhang, Yime [1 ]
He, Jing [3 ]
Zhong, Chao [1 ]
机构
[1] Peking Univ, Inst Syst Biomed, Hlth Sci Ctr, Sch Basic Med Sci,Dept Immunol,NHC Key Lab Med Imm, Beijing 100191, Peoples R China
[2] Peking Univ, Inst Syst Biomed, Hlth Sci Ctr, Beijing 100191, Peoples R China
[3] Peking Univ, Peoples Hosp, Dept Rheumatol & Immunol, Beijing Key Lab Rheumatism Mech & Immune Diag, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
NK CELLS; TRANSCRIPTIONAL REPRESSOR; INNATE; EXPRESSION; DIFFERENTIATION; ACTIVATION; PROGENITOR; RESPONSES; MIZ-1; STEM;
D O I
10.1016/j.isci.2023.107187
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Tissue-residential natural killer (trNK) cells act as pioneering responders during infectious challenges. However, their discrimination with conventional NK (cNK) cells is still an issue. Through an integrative transcriptome comparison of the two NK subgroups from different tissues, we have defined two genesets capable of efficiently distinguishing them. Based on the two genesets, a fundamental difference between the activation of trNK and cNK is identified and further confirmed. Mechanistically, we have discovered a particular role of chromatin landscape in regulating the trNK activation. In addition, IL-21R and IL-18R are respectively highly expressed by trNK and cNK, indicating a role of cytokine milieu in determining their differential activation. Indeed, IL-21 is particularly critical in accessorily promoting trNK activation using a bunch of bifunctional transcription factors. Together, this study sheds light on the bona fide difference between trNK and cNK, which will further expand our knowledge about their distinct functionalities during immune responses.
引用
收藏
页数:23
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