| Literature DB >> 33448928 |
Danielle Janosevic1, Jered Myslinski1, Thomas W McCarthy1, Amy Zollman1, Farooq Syed2, Xiaoling Xuei3, Hongyu Gao3, Yun-Long Liu3, Kimberly S Collins1, Ying-Hua Cheng1, Seth Winfree1, Tarek M El-Achkar1,4, Bernhard Maier1, Ricardo Melo Ferreira1, Michael T Eadon1, Takashi Hato1, Pierre C Dagher1,4.
Abstract
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.Entities:
Keywords: acute kidney injury; human; immunology; inflammation; medicine; mouse; sepsis; single-cell RNA-seq
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Year: 2021 PMID: 33448928 PMCID: PMC7810465 DOI: 10.7554/eLife.62270
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.140