ZFIN ID: ZDB-PUB-200301-3
Zebrafish GSDMEb Cleavage-Gated Pyroptosis Drives Septic-Acute Kidney Injury In Vivo
Wang, Z., Gu, Z., Hou, Q., Chen, W., Mu, D., Zhang, Y., Liu, Q., Liu, Z., Yang, D.
Date: 2020
Source: Journal of immunology (Baltimore, Md. : 1950)   204(7): 1929-1942 (Journal)
Registered Authors: Hou, Qing, Liu, Zhihong, Yang, Dahai
Keywords: none
MeSH Terms:
  • Acute Kidney Injury/metabolism*
  • Animals
  • Animals, Genetically Modified/metabolism
  • Caspases/metabolism
  • HEK293 Cells
  • Humans
  • Immunity, Innate/physiology
  • Kidney Tubules/metabolism
  • Lipopolysaccharides/metabolism
  • Mice
  • Mice, Inbred C57BL
  • Multiple Organ Failure/metabolism
  • Phosphate-Binding Proteins/metabolism*
  • Pyroptosis/physiology*
  • Sepsis/metabolism*
  • Zebrafish
  • Zebrafish Proteins/metabolism
PubMed: 32111733 Full text @ J. Immunol.
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ABSTRACT
The bacteria LPS is one of the leading endotoxins responsible for sepsis; its sensing pathway-induced pyroptosis plays an important role in innate immunity. However, excessive pyroptosis might cause immunological diseases, even multiple organ failure and death by undefined mechanisms. Given that the development of acute kidney injury (AKI) in patients with sepsis causes significant morbidity and mortality, the mechanism of pyroptosis in regulating septic AKI remains unknown. In this study, we establish a zebrafish crispant in vivo analysis model and reveal that both caspy2 and gasdermin Eb (GSDMEb) contribute to lethal LPS-induced septic shock. Meanwhile, the in vitro analysis reveals that caspy2 activation can specifically cleave GSDMEb to release its N terminus to mediate pyroptosis, which functions as GSDMD in mammals. Interestingly, we establish an in vivo propidium iodide-staining method and reveal that the caspy2-GSDMEb signaling cascade is essential for enhancing renal tubular damage during lethal LPS-induced septic shock, whereas administration of the zebrafish-specific GSDMEb-derived peptide inhibitor Ac-FEID-CMK can attenuate mortality and septic AKI in vivo. Moreover, we confirm that either caspase-11 or GSDMD deficiency decreases both inflammatory cytokines and kidney dysfunction enzyme release and prolongs survival in a murine model of septic shock. Taken together, these findings demonstrate an evolutionary executor for pyroptosis in zebrafish and reveal that the pyroptosis of renal tubular cells is a major cause of septic AKI, and also provide an ideal in vivo screening model for potential antisepsis therapeutic strategies.
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