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Interferon-gamma regulates inflammatory cell death by targeting necroptosis in experimental autoimmune arthritis
Interferon-gamma regulates inflammatory cell death by targeting necroptosis in experimental autoimmune arthritis
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Interferon-gamma regulates inflammatory cell death by targeting necroptosis in experimental autoimmune arthritis
Interferon-gamma regulates inflammatory cell death by targeting necroptosis in experimental autoimmune arthritis

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Interferon-gamma regulates inflammatory cell death by targeting necroptosis in experimental autoimmune arthritis
Interferon-gamma regulates inflammatory cell death by targeting necroptosis in experimental autoimmune arthritis
Journal Article

Interferon-gamma regulates inflammatory cell death by targeting necroptosis in experimental autoimmune arthritis

2017
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Overview
Interferon γ (IFN-γ) induces an inflammatory response and apoptotic cell death. Rheumatoid arthritis (RA) is a systemic inflammatory disease associated with increased levels of inflammatory mediators, including tumour necrosis factor α (TNF-α) and T helper (Th) 17 cells, and downregulation of apoptosis of inflammatory cells. We hypothesized that IFN-γ would reduce inflammatory cell death in vitro and that loss of IFN-γ would aggravate inflammation in vivo . IFN-γ downregulated necroptosis and the expression of cellular FLICE-like inhibitory protein (cFLIP L ) and mixed lineage kinase domain-like (MLKL). However, loss of IFN-γ promoted the production of cFLIP L and MLKL, and necroptosis. IFN-γ deficiency increased Th17 cell number and upregulated the expression of IL-17 and TNF-α. Expression of MLKL, receptor interacting protein kinase (RIPK)1, and RIPK3 was increased in the joints of mice with collagen-induced arthritis (CIA). Compared with wild-type mice with CIA, IFN-γ −/− CIA mice showed exacerbation of cartilage damage and joint inflammation, and acceleration of MLKL, RIPK1, and RIPK3 production in the joints. IFN-γ deficiency induced the activation of signal transducer and activator of transcription 3. These results suggest that IFN-γ regulates inflammatory cell death and may have potential for use in the treatment of RA.