High-Mobility Group Box 1 Is Dispensable for Autophagy, Mitochondrial Quality Control, and Organ Function In Vivo

• DOI: 10.1016/j.cmet.2014.01.014
• Publication Date: 2014-03-04T23:33:15Z
• Authors: Peter Huebener; Geum-Youn Gwak; Jean-Philippe Pra...; Catarina M. Quinzii; Richard Friedman; Chyuan-Sheng Lin; Chad M. Trent; Ingmar Mederacke; Enpeng Zhao; Dianne H. Dapito; Yuxi Lin; Ira J. Goldberg; Mark J. Czaja; Robert F. Schwabe
• Keywords: Blood Glucose; 0301 basic medicine; Physiology; Gene Expression; Mice, Transgenic; Cell Biology; Oxidative Phosphorylation; Mitochondria; Mice; 03 medical and health sciences; Adenosine Triphosphate; Liver; Autophagy; Animals; Myocytes, Cardiac; RNA, Messenger; HMGB1 Protein; Energy Metabolism; Molecular Biology

In vitro studies have demonstrated a critical role for high-mobility group box 1 (HMGB1) in autophagy and the autophagic clearance of dysfunctional mitochondria, resulting in severe mitochondrial fragmentation and profound disturbances of mitochondrial respiration in HMGB1-deficient cells. Here, we investigated the effects of HMGB1 deficiency on autophagy and mitochondrial function in vivo, using conditional Hmgb1 ablation in the liver and heart. Unexpectedly, deletion of Hmgb1 in hepatocytes or cardiomyocytes, two cell types with abundant mitochondria, did not alter mitochondrial structure or function, organ function, or long-term survival. Moreover, hepatic autophagy and mitophagy occurred normally in the absence of Hmgb1, and absence of Hmgb1 did not significantly affect baseline and glucocorticoid-induced hepatic gene expression. Collectively, our findings suggest that HMGB1 is dispensable for autophagy, mitochondrial quality control, the regulation of gene expression, and organ function in the adult organism.