CD4-CD8-双阴性T细胞在非酒精性脂肪性肝病中的关键和多样化作用

Abstract

Background & Aims Hepatic inflammation is a hallmark of nonalcoholic fatty liver disease (NAFLD). Double negative T (DNT) cells are a unique subset of T lymphocytes that do not express CD4, CD8, or natural killer cell markers, and studies have suggested that DNT cells play critical and diverse roles in the immune system. However, the role of intrahepatic DNT cells in NAFLD is largely unknown. Methods The proportions and RNA transcription profiling of intrahepatic DNT cells were compared between C57BL/6 mice fed with control diet or methionine-choline–deficient diet for 5 weeks. The functions of DNT cells were tested in vitro and in vivo. Results The proportion of intrahepatic DNT cells was significantly increased in mice with diet-induced NAFLD. In NAFLD mice, the proportion of intrahepatic TCRγδ + DNT cells was increased along with elevated interleukin (IL) 17A; in contrast, the percentage of TCRαβ + DNT cells was decreased, accompanied by reduced granzyme B (GZMB). TCRγδ + DNT cell depletion resulted in lowered liver IL17A levels and significantly alleviated NAFLD. Adoptive transfer of intrahepatic TCRαβ + DNT cells from control mice increased intrahepatic CD4 and CD8 T cell apoptosis and inhibited NAFLD progression. Furthermore, we revealed that adrenic acid and arachidonic acid, harmful fatty acids that were enriched in the liver of the mice with NAFLD, could induce apoptosis of TCRαβ + DNT cells and inhibit their immunosuppressive function and nuclear factor kappa B (NF-κB) or AKT signaling pathway activity. However, arachidonic acid facilitated IL17A secretion by TCRγδ + DNT cells, and the NF-κB signaling pathway was involved. Finally, we also confirmed the variation of intrahepatic TCRαβ + DNT cells and TCRγδ + DNT cells in humans. Conclusions During NAFLD progression, TCRγδ + DNT cells enhance IL17A secretion and aggravate liver inflammation, whereas TCRαβ + DNT cells decrease GZMB production and lead to weakened immunoregulatory function. Shiftin