The C3/C3aR pathway exacerbates acetaminophen-induced mouse liver injury via upregulating podoplanin on the macrophage

FASEB J. 2025 Jan 15;39(1):e70272. doi: 10.1096/fj.202402278RR.

Abstract

Acute liver failure (ALF) is a life-threatening condition that occurs when the liver sustains severe damage and rapidly loses its function. The primary cause of ALF is the overdose of acetaminophen (APAP), and its treatment is relatively limited. The involvement of the complement system in the development of ALF has been implicated. However, the related mechanisms remain poorly understood. Complement 3 (C3) knockout mice, complement 3a receptor (C3aR) knockout mice, platelet C-type lectin-like receptor 2 (Clec-2)-deficient mice, and myeloid cell podoplanin (Pdpn)-deficient mice were generated. Liver tissues were collected for histological analysis, RNA sequencing, confocal immunofluorescence, and immunoblot analyses. Our data demonstrated that APAP activated the C3/C3aR pathway, leading to intrahepatic hemorrhage, ultimately resulting in hepatocyte necrosis. Deletion of C3 or C3aR mitigated APAP-induced liver injury (AILI). C3/C3aR signaling upregulated the expression and phosphorylation of transcription factors STAT3 and c-Fos in hepatic Kupffer cells, which in turn increased PDPN expression, promoting platelet recruitment to the Kupffer cells via the interaction of PDPN and the CLEC-2 on platelets. Since the activation of platelets mediated by C3/C3aR occurs irrespective of the major hemostatic pathways, blocking the C3/C3aR pathway in ALF could be a coagulopathy-sparing and novel therapeutic approach. In summary, this study unveiled the critical roles of the C3/C3aR pathway in developing AILI, providing evidence that the C3/C3aR pathway could be an effective therapeutic target for AILI.

Keywords: C3/C3aR pathway; CLEC‐2; Kupffer cell; PDPN; liver injury.

MeSH terms

  • Acetaminophen* / adverse effects
  • Acetaminophen* / toxicity
  • Animals
  • Chemical and Drug Induced Liver Injury* / metabolism
  • Chemical and Drug Induced Liver Injury* / pathology
  • Complement C3* / genetics
  • Complement C3* / metabolism
  • Kupffer Cells / drug effects
  • Kupffer Cells / metabolism
  • Lectins, C-Type* / genetics
  • Lectins, C-Type* / metabolism
  • Liver / drug effects
  • Liver / metabolism
  • Liver / pathology
  • Macrophages / drug effects
  • Macrophages / metabolism
  • Male
  • Membrane Glycoproteins* / genetics
  • Membrane Glycoproteins* / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout*
  • Receptors, Complement / genetics
  • Receptors, Complement / metabolism
  • STAT3 Transcription Factor / metabolism
  • Signal Transduction
  • Up-Regulation / drug effects

Substances

  • Acetaminophen
  • Gp38 protein, mouse
  • Membrane Glycoproteins
  • Complement C3
  • Lectins, C-Type
  • Receptors, Complement
  • CLEC-2 protein, mouse
  • STAT3 Transcription Factor
  • C3 protein, mouse
  • complement C3a receptor