4.3 Article

The dynamics of cell death patterns and regeneration during acute liver injury in mice

Journal

FEBS OPEN BIO
Volume 12, Issue 5, Pages 1061-1074

Publisher

WILEY
DOI: 10.1002/2211-5463.13383

Keywords

acute liver injury; cell death; cytokines; hepatocyte; prognosis; regeneration

Funding

  1. National Natural Science Foundation of China [81870429, 82170630, 32171125, 81971331, 81800542]
  2. National 13th 5-Year Plan for Hepatitis Research [2017ZX10203201-007]
  3. Natural Science Foundation of Tianjin [19JCZDJC36700]
  4. Science & Technology Development Fund of Tianjin Education Commission for Higher Education [2019KJ170]

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The study revealed that acute liver injury induced by CCl4 had three phases - early, progressive, and recovery - with different cell death patterns and regeneration dynamics. On the other hand, acute liver injury induced by D-gal/LPS only had early and progressive phases, leading to severe liver damage with high mortality. These findings provide valuable insights for clinical therapy and prognosis.
Acute liver injury is a serious clinical syndrome with multiple causes and unclear pathological process. Here, CCl4- and D-galactosamine/lipopolysaccharide (D-gal/LPS)-induced acute liver injury was established to explore the cell death patterns and determine whether or not liver regeneration occurred. In CCl4-induced hepatic injury, three phases, including the early, progressive, and recovery phase, were considered based on alterations of serum transaminases and liver morphology. Moreover, in this model, cytokines exhibited double-peak fluctuations; apoptosis and pyroptosis persisted throughout all phases; autophagy occurred in the early and the progressive phases; and sufficient and timely hepatocyte regeneration was observed only during the recovery phase. All of these phenomena contribute to mild liver injury and subsequent regeneration. Strikingly, only the early and progressive phases were observed in the D-gal/LPS model. Slight pyroptosis occurred in the early phase but diminished in the progressive phase, while apoptosis, reduced autophagy, and slight but subsequently diminished regeneration occurred only during the progressive phase, accompanied by a strong cytokine storm, resulting in severe liver injury with high mortality. Taken together, our work reveals variable modes and dynamics of cell death and regeneration, which lead to different consequences for mild and severe acute liver injury, providing a helpful reference for clinical therapy and prognosis.

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