Diurnal Rhythms Spatially and Temporally Organize Autophagy
Mikhail Ryzhikov,
Anna Ehlers,
Deborah Steinberg,
Wenfang Xie,
Eitan Oberlander,
Samuel Brown,
Petra E. Gilmore,
Reid R. Townsend,
William S. Lane,
Tamas Dolinay,
Kiichi Nakahira,
Augustine M.K. Choi,
Jeffrey A. Haspel
Affiliations
Mikhail Ryzhikov
Division of Pulmonary and Critical Care Medicine, Washington University School of Medicine, Campus Box 8052, 660 South Euclid Avenue, St. Louis, MO 63110, USA
Anna Ehlers
Division of Pulmonary and Critical Care Medicine, Washington University School of Medicine, Campus Box 8052, 660 South Euclid Avenue, St. Louis, MO 63110, USA
Deborah Steinberg
Division of Pulmonary and Critical Care Medicine, Washington University School of Medicine, Campus Box 8052, 660 South Euclid Avenue, St. Louis, MO 63110, USA
Wenfang Xie
Division of Pulmonary and Critical Care Medicine, Washington University School of Medicine, Campus Box 8052, 660 South Euclid Avenue, St. Louis, MO 63110, USA; Department of Respiration, Integrated Hospital of Traditional Chinese Medicine, Southern Medical University, Guangzhou, Guangdong 510315, China
Eitan Oberlander
Division of Pulmonary and Critical Care Medicine, Washington University School of Medicine, Campus Box 8052, 660 South Euclid Avenue, St. Louis, MO 63110, USA
Samuel Brown
Division of Pulmonary and Critical Care Medicine, Washington University School of Medicine, Campus Box 8052, 660 South Euclid Avenue, St. Louis, MO 63110, USA
Petra E. Gilmore
Division of Endocrinology, Metabolism and Lipid Research, Washington University School of Medicine, Campus Box 8052, 660 South Euclid Avenue, St. Louis, MO 63110, USA
Reid R. Townsend
Division of Endocrinology, Metabolism and Lipid Research, Washington University School of Medicine, Campus Box 8052, 660 South Euclid Avenue, St. Louis, MO 63110, USA
William S. Lane
Harvard University Mass Spectrometry & Proteomics Laboratory, Cambridge, MA 02138, USA
Tamas Dolinay
Division of Pulmonary and Critical Care Medicine, UCLA Medical Center, 2625 W. Alameda Avenue, Burbank, CA 91505, USA
Kiichi Nakahira
Department of Medicine, New York Presbyterian/Weill Cornell Medical Center, 555 E. 68 St., New York, NY 10065, USA
Augustine M.K. Choi
Department of Medicine, New York Presbyterian/Weill Cornell Medical Center, 555 E. 68 St., New York, NY 10065, USA
Jeffrey A. Haspel
Division of Pulmonary and Critical Care Medicine, Washington University School of Medicine, Campus Box 8052, 660 South Euclid Avenue, St. Louis, MO 63110, USA; Corresponding author
Summary: Circadian rhythms are a hallmark of physiology, but how such daily rhythms organize cellular catabolism is poorly understood. Here, we used proteomics to map daily oscillations in autophagic flux in mouse liver and related these rhythms to proteasome activity. We also explored how systemic inflammation affects the temporal structure of autophagy. Our data identified a globally harmonized rhythm for basal macroautophagy, chaperone-mediated autophagy, and proteasomal activity, which concentrates liver proteolysis during the daytime. Basal autophagy rhythms could be resolved into two antiphase clusters that were distinguished by the subcellular location of targeted proteins. Inflammation induced by lipopolysaccharide reprogrammed autophagic flux away from a temporal pattern that favors cytosolic targets and toward the turnover of mitochondrial targets. Our data detail how daily biological rhythms connect the temporal, spatial, and metabolic aspects of protein catabolism. : How circadian rhythms contribute to cellular quality control is poorly understood. Ryzhikov et al. mapped proteome-wide biological rhythms in liver autophagy and identified synchronous daily oscillations in autophagic and proteasomal activity. Diurnal rhythms play a role in autophagy substrate selection based on subcellular location and inflammation status. Keywords: macroautophagy, autophagy, chaperone-mediated autophagy, proteasome, circadian rhythm, lipopolysaccharide, endotoxin, inflammation, clock