Department of Pediatrics and the Herman B. Wells Center, Indiana University School of Medicine, Indianapolis, United States
Xiaoling Xuei
Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, United States
Hongyu Gao
Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, United States
Yun-Long Liu
Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, United States
Kimberly S Collins
Department of Medicine, Indiana University School of Medicine, Indianapolis, United States
Ying-Hua Cheng
Department of Medicine, Indiana University School of Medicine, Indianapolis, United States
Seth Winfree
Department of Medicine, Indiana University School of Medicine, Indianapolis, United States
Tarek M El-Achkar
Department of Medicine, Indiana University School of Medicine, Indianapolis, United States; Roudebush Indianapolis Veterans Affairs Medical Center, Indianapolis, United States
Department of Medicine, Indiana University School of Medicine, Indianapolis, United States
Pierre C Dagher
Department of Medicine, Indiana University School of Medicine, Indianapolis, United States; Roudebush Indianapolis Veterans Affairs Medical Center, Indianapolis, United States
Sepsis is a dynamic state that progresses at variable rates and has life-threatening consequences. Staging patients along the sepsis timeline requires a thorough knowledge of the evolution of cellular and molecular events at the tissue level. Here, we investigated the kidney, an organ central to the pathophysiology of sepsis. Single-cell RNA-sequencing in a murine endotoxemia model revealed the involvement of various cell populations to be temporally organized and highly orchestrated. Endothelial and stromal cells were the first responders. At later time points, epithelial cells upregulated immune-related pathways while concomitantly downregulating physiological functions such as solute homeostasis. Sixteen hours after endotoxin, there was global cell–cell communication failure and organ shutdown. Despite this apparent organ paralysis, upstream regulatory analysis showed significant activity in pathways involved in healing and recovery. This rigorous spatial and temporal definition of murine endotoxemia will uncover precise biomarkers and targets that can help stage and treat human sepsis.