| Literature DB >> 26422992 |
Ling Tang1, Hui Peng2, Jing Zhou1, Yongyan Chen1, Haiming Wei1, Rui Sun3, Wayne M Yokoyama4, Zhigang Tian5.
Abstract
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.Entities:
Keywords: Conventional NK cell; Cytotoxicity; ILC1; Liver-resident NK cell; Phenotype
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Year: 2015 PMID: 26422992 DOI: 10.1016/j.jaut.2015.09.004
Source DB: PubMed Journal: J Autoimmun ISSN: 0896-8411 Impact factor: 7.094