In vivo hepatic differentiation potential of human cord blood-derived mesenchymal stem cells

Int J Mol Med. 2011 May;27(5):701-6. doi: 10.3892/ijmm.2011.627. Epub 2011 Feb 23.

Abstract

Although recent studies have demonstrated the in vitro hepatic differentiation potential of mesenchymal stem cells (MSCs), the evidence supporting the in vivo engraftment of MSCs, hepatic differentiation and improvement of hepatic function is still lacking. We investigated in vivo hepatic differentiation potential and therapeutic effect of cord blood derived-MSCs (CBMSCs) transplantation in a cirrhotic rat model. CBMSCs (2 x 10(6)) were infused in Wistar rats with thioacetamide-induced chronic liver injury. Biochemical markers, liver fibrosis and engraftment of CBMSCs were assessed. Infused CBMSCs were detected in the perivascular or fibrous region of the liver and did not acquire mature hepatic phenotypes. There was no difference in biochemical markers and in the area of liver fibrosis between the experimental and placebo groups. After infusion of CBMSCs in our experimental cirrhotic rat model we did not observe an improvement of liver function and liver fibrosis. Inversely, CBMSCs could have a pro-fibrogenic potential suggesting that a cautious approach is required in future research.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alanine Transaminase / blood
  • Ammonia / blood
  • Animals
  • Antigens, Differentiation / metabolism
  • Aspartate Aminotransferases / blood
  • Bilirubin / blood
  • Cell Differentiation
  • Female
  • Fetal Blood / cytology*
  • Humans
  • Liver / pathology*
  • Liver / physiopathology
  • Liver Cirrhosis, Experimental / chemically induced
  • Liver Cirrhosis, Experimental / pathology
  • Liver Cirrhosis, Experimental / therapy
  • Mesenchymal Stem Cell Transplantation*
  • Mesenchymal Stem Cells / cytology*
  • Rats
  • Rats, Wistar
  • Serum Albumin / metabolism
  • Thioacetamide

Substances

  • Antigens, Differentiation
  • Serum Albumin
  • Thioacetamide
  • Ammonia
  • Aspartate Aminotransferases
  • Alanine Transaminase
  • Bilirubin