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Publication Information
Affiliation
Department of Surgery, University of Pittsburgh, Pittsburgh, PA, 15213, USA.; Department of Surgery, University of Pittsburgh, Pittsburgh, PA, 15213, USA.; Department of Surgery, University of Pittsburgh, Pittsburgh, PA, 15213, USA.; Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, 60611, USA.; Department of Pediatrics, University of Alabama at Birmingham, Birmingham, AL, 35233, USA.; Department of Surgery, University of Pittsburgh, Pittsburgh, PA, 15213, USA.; Department of Surgery, University of Pittsburgh, Pittsburgh, PA, 15213, USA.; Department of Surgery, University of Pittsburgh, Pittsburgh, PA, 15213, USA.; Department of Pediatrics, University of Pittsburgh, Pittsburgh, PA, 15213, USA.; Department of Surgery, University of Pittsburgh, Pittsburgh, PA, 15213, USA. vodovotzy@upmc.edu.
Authors
Zamora Ruben, Barclay Derek, Yin Jinling, Alonso Estella M, Leonis Mike A, Mi Qi, Billiar Timothy R, Simmons Richard L, Squires Robert H, Vodovotz Yoram
Studies
Abstract
Acetaminophen (APAP) overdose (APAPo) is predominant in the NIH Pediatric Acute Liver Failure (PALF) Study. We assayed multiple inflammatory mediators in serial serum samples from 13 PALF survivors with APAPo + N-acetylcysteine (NAC, the frontline therapy for APAPo), 8 non-APAPo + NAC, 40 non-APAPo non-NAC, and 12 non-survivors. High Mobility Group Box 1 (HMGB1) was a dominant mediator in dynamic inflammation networks in all sub-groups, associated with a threshold network complexity event at d1-2 following enrollment that was exceeded in non-survivors vs. survivors. We thus hypothesized that differential HMGB1 network connectivity after day 2 is related to the putative threshold event in non-survivors. DyNA showed that HMGB1 is most connected in non-survivors on day 2-3, while no connections were observed in APAPo + NAC and non-APAPo + NAC survivors. Inflammatory dynamic networks, and in particular HMGB1 connectivity, were associated with the use of NAC in the context of APAPo. To recapitulate hepatocyte (HC) damage in vitro, primary C57BL/6 HC and HC-specific HMGB1-null HC were treated with APAP + NAC. Network phenotypes of survivors were recapitulated in C57BL/6 mouse HC and were greatly altered in HMGB1-null HC. HC HMGB1 may thus coordinate a pro-inflammatory program in PALF non-survivors (which is antagonized by NAC), while driving an anti-inflammatory/repair program in survivors.