TXNIP Regulates Natural Killer Cell-Mediated Innate Immunity by Inhibiting IFN-γ Production during Bacterial Infection

TXNIP通过抑制细菌感染期间IFN-γ的产生来调节自然杀伤细胞介导的先天免疫

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作者:Dong Oh Kim,Jae-Eun Byun,Won Sam Kim,Mi Jeong Kim,Jung Ha Choi,Hanna Kim,Eunji Choi,Tae-Don Kim,Suk Ran Yoon,Ji-Yoon Noh,Young-Jun Park,Jungwoon Lee,Hee Jun Cho,Hee Gu Lee,Sang-Hyun Min,Inpyo Choi,Haiyoung Jung

Abstract

The function of natural killer (NK) cell-derived interferon-γ (IFN-γ) expands to remove pathogens by increasing the ability of innate immune cells. Here, we identified the critical role of thioredoxin-interacting protein (TXNIP) in the production of IFN-γ in NK cells during bacterial infection. TXNIP inhibited the production of IFN-γ and the activation of transforming growth factor β-activated kinase 1 (TAK1) activity in primary mouse and human NK cells. TXNIP directly interacted with TAK1 and inhibited TAK1 activity by interfering with the complex formation between TAK1 and TAK1 binding protein 1 (TAB1). Txnip-/- (KO) NK cells enhanced the activation of macrophages by inducing IFN-γ production during Pam3CSK4 stimulation or Staphylococcus aureus (S. aureus) infection and contributed to expedite the bacterial clearance. Our findings suggest that NK cell-derived IFN-γ is critical for host defense and that TXNIP plays an important role as an inhibitor of NK cell-mediated macrophage activation by inhibiting the production of IFN-γ during bacterial infection.

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