先天性淋巴细胞
生物
细胞毒性T细胞
免疫学
Janus激酶3
白细胞介素12
白细胞介素21
归巢(生物学)
淋巴因子激活杀伤细胞
细胞生物学
免疫系统
先天免疫系统
表型
体外
T细胞
基因
遗传学
生态学
作者
Ling Tang,Hui Peng,Jing Zhou,Yongyan Chen,Haiming Wei,Rui Sun,Wayne M. Yokoyama,Zhigang Tian
标识
DOI:10.1016/j.jaut.2015.09.004
摘要
Group 1 innate lymphoid cells (ILCs) consist of conventional natural killer (cNK) cells, tissue-resident NK cells and mucosal ILC1s. Recently identified liver-resident NK cells, which can mount contact hypersensitivity responses, and mucosal ILC1s that are involved in pathogenesis of colitis are distinct from cNK cells in several aspects, but the issue of how they are related to each other has not been clearly clarified. Here, we show that liver-resident NK cells and mucosal ILC1s have different phenotypes, as evidenced by distinct expression patterns of homing-associated molecules. Moreover, mucosal ILC1s exhibit tissue residency akin to liver-resident NK cells. Importantly, liver-resident NK cells express relative high levels of cytotoxic effector molecules, which are poorly expressed by mucosal ILC1s, and exhibit stronger cytotoxic activity compared with mucosal ILC1s. These results demonstrate differential phenotypic and functional characteristics of liver-resident NK cells and mucosal ILC1s, shedding new light on the diversity of ILC family.
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