| Literature DB >> 28228283 |
Selma Boulenouar1, Xavier Michelet1, Danielle Duquette2, David Alvarez3, Andrew E Hogan4, Christina Dold5, Donal O'Connor4, Suzanne Stutte3, Ali Tavakkoli2, Desmond Winters4, Mark A Exley2, Donal O'Shea4, Michael B Brenner2, Ulrich von Andrian3, Lydia Lynch6.
Abstract
Adipose tissue has a dynamic immune system that adapts to changes in diet and maintains homeostatic tissue remodeling. Adipose type 1 innate lymphoid cells (AT1-ILCs) promote pro-inflammatory macrophages in obesity, but little is known about their functions at steady state. Here we found that human and murine adipose tissue harbor heterogeneous populations of AT1-ILCs. Experiments using parabiotic mice fed a high-fat diet (HFD) showed differential trafficking of AT1-ILCs, particularly in response to short- and long-term HFD and diet restriction. At steady state, AT1-ILCs displayed cytotoxic activity toward adipose tissue macrophages (ATMs). Depletion of AT1-ILCs and perforin deficiency resulted in alterations in the ratio of inflammatory to anti-inflammatory ATMs, and adoptive transfer of AT1-ILCs exacerbated metabolic disorder. Diet-induced obesity impaired AT1-ILC killing ability. Our findings reveal a role for AT1-ILCs in regulating ATM homeostasis through cytotoxicity and suggest that this function is relevant in both homeostasis and metabolic disease.Entities:
Keywords: NK cells; adipose tissue; cytotoxicity; macrophages; metabolism; obesity
Mesh:
Year: 2017 PMID: 28228283 DOI: 10.1016/j.immuni.2017.01.008
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745