Human umbilical cord mesenchymal stromal cells rescue mice from acetaminophen-induced acute liver failure

Cytotherapy. 2014 Sep;16(9):1207-19. doi: 10.1016/j.jcyt.2014.05.018.

Abstract

Background aims: Acute liver failure (ALF), a life-threatening disease characterized by the sudden loss of hepatic function, can occur after an accidental or intentional acetaminophen overdose.

Methods: With the use of an ALF mouse model, we examined both the preventive and therapeutic potential of intravenously administered human umbilical cord-derived mesenchymal stromal cells (hUCMSCs). Primary hUCMSCs were purified from freshly collected full-term umbilical cords and intravenously transplanted into BALB/c mice either before and after ALF induced by acetaminophen intoxication. We found that hUCMSCs significantly improved survival rates and relative liver weight of mice in both pre-ALF and post-ALF animals. Correspondingly, serum levels of markers that reflect hepatic injury (ie, aspartate aminotransferase, alanine aminotransferase and total bilirubin) were significantly attenuated in the group receiving hUCMSC therapy.

Results: Mechanistically, we found that the protective potential of intravenously administered hUCMSCs was mediated by paracrine pathways that involved antioxidants (glutathione, superoxide dismutase), the reduction of inflammatory agents (tumor necrosis factor-α, interleukin-6) and elevated serum levels of hepatocyte growth factor.

Conclusions: Through these paracrine effects, intravenously administered hUCMSCs reduced hepatic necrosis/apoptosis and enhanced liver regeneration. Thus, our data demonstrate that intravenously administered hUCMSCs may be useful in the prevention or treatment of acetaminophen-induced ALF.

Keywords: acute liver failure; anti-inflammation; antioxidants; apoptosis; hepatic regeneration; umbilical cord mesenchymal stromal cells.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Acetaminophen / administration & dosage
  • Acetaminophen / toxicity*
  • Administration, Intravenous
  • Alanine Transaminase / blood
  • Animals
  • Aspartate Aminotransferases / blood
  • Bilirubin / blood
  • Cell Differentiation
  • Cells, Cultured
  • Disease Models, Animal
  • Humans
  • Liver / metabolism*
  • Liver / pathology
  • Liver Failure, Acute / chemically induced
  • Liver Failure, Acute / therapy*
  • Male
  • Mesenchymal Stem Cell Transplantation*
  • Mesenchymal Stem Cells / physiology*
  • Mice, Inbred BALB C
  • Umbilical Cord / cytology

Substances

  • Acetaminophen
  • Aspartate Aminotransferases
  • Alanine Transaminase
  • Bilirubin