The orchestrated cellular and molecular responses of the kidney to endotoxin define a precise sepsis timeline.
Danielle JanosevicJered MyslinskiThomas W McCarthyAmy ZollmanFarooq SyedXiaoling XueiHongyu GaoYun-Long LiuKimberly S CollinsYing-Hua ChengSeth WinfreeTarek M El-AchkarBernhard MaierRicardo Melo FerreiraMichael T EadonTakashi HatoPierre C DagherPublished in: eLife (2021)
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.
Keyphrases
- single cell
- rna seq
- septic shock
- acute kidney injury
- intensive care unit
- high throughput
- endothelial cells
- cell therapy
- end stage renal disease
- newly diagnosed
- healthcare
- ejection fraction
- chronic kidney disease
- stem cells
- lymph node
- magnetic resonance
- peritoneal dialysis
- high resolution
- drug induced
- mesenchymal stem cells
- induced pluripotent stem cells
- patient reported