Arts, Rob J. W. Huang, Po-Kai Yang, De A. B. Joosten, Leo van der Meer, Jos W. M. J. Oppenheim, Joost G. Netea, Mihai Cheng, Shih-Chin data_sheet_1.docx <p>High-mobility group nucleosome-binding protein 1 (HMGN1) functions as a non-histone chromatin-binding protein in the cell nucleus. However, extracellular HMGN1 acts as an endogenous danger-associated inflammatory mediator (also called alarmin). We demonstrated that HMGN1 not only directly stimulated cytokine production but also had the capacity to induce immune tolerance by a TLR4-dependent pathway, similar to lipopolysaccharide (LPS)-induced tolerance. HMGN1-induced tolerance was accompanied by a metabolic shift associated with the inhibition of the induction of Warburg effect (aerobic glycolysis) and histone deacetylation via Sirtuin-1. In addition, HMGN1 pre-challenge of mice also downregulated TNF production similar to LPS-induced tolerance in vivo. In conclusion, HMGN1 is an endogenous TLR4 ligand that can induce both acute stimulation of cytokine production and long-term tolerance, and thus it might play a modulatory role in sterile inflammatory processes such as those induced by infection, trauma, or ischemia.</p> high-mobility group nucleosome-binding protein 1;endotoxin tolerance;sterile inflammation;sirtuin-1;macrophages 2018-03-14
    https://frontiersin.figshare.com/articles/dataset/data_sheet_1_docx/5980531
10.3389/fimmu.2018.00526.s001