CD133+ stem cell mobilization after partial hepatectomy depends on resection extent and underlying disease

Dig Liver Dis. 2011 Feb;43(2):147-54. doi: 10.1016/j.dld.2010.06.008. Epub 2010 Aug 4.

Abstract

Background: Bone marrow stem cells (BMSC) can participate to liver regeneration. However, conflicting results have been reported on this topic in patients undergoing liver resection.

Aims: To assess the impact of liver resection extent and presence of underlying liver disease in modulating BMSC mobilization.

Methods: We enrolled 29 patients undergoing liver resection of different extents, 5 surgical controls and 10 blood donors. Circulating CD133+ BMSC were measured by flow cytometry at different time-points after surgery. The hepatic commitment of mobilized BMSC was investigated by polymerase chain reaction. Liver specimens were collected during surgery for histopathological analysis. Hepatocyte growth factor and granulocyte-colony stimulating factor serum levels were measured by enzyme-linked immunosorbent assay.

Results: BMSC mobilization was found in patients undergoing major liver resection, especially in the presence of underlying disease. Ductular reactions were noted in patients with chronic hepatopathy and the hepatic progenitor-like cells expressed CD133, NCAM, cytokeratin-19, and alpha-fetoprotein. Hepatocyte growth factor and granulocyte-colony stimulating factor levels increased following liver resection and the contemporaneous presence of liver disease was associated with their highest raise.

Conclusions: Liver repair is mainly an endogenous process. BMSC become important in case of extensive resection, especially in the presence of underlying hepatopathy and hepatic progenitor-like cells activation. Hepatocyte growth factor and granulocyte-colony stimulating factor seem to be involved in the dynamics underlying hepatic regeneration and BMSC recruitment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AC133 Antigen
  • Antigens, CD / blood*
  • Biomarkers / blood
  • Case-Control Studies
  • Female
  • Glycoproteins / blood*
  • Granulocyte Colony-Stimulating Factor / blood
  • Hematopoietic Stem Cell Mobilization*
  • Hepatectomy / methods*
  • Hepatocyte Growth Factor / blood
  • Humans
  • Keratin-19 / blood
  • Liver Diseases / surgery
  • Liver Regeneration*
  • Male
  • Middle Aged
  • Neural Cell Adhesion Molecules / blood
  • Peptides / blood*
  • alpha-Fetoproteins / metabolism

Substances

  • AC133 Antigen
  • Antigens, CD
  • Biomarkers
  • Glycoproteins
  • Keratin-19
  • Neural Cell Adhesion Molecules
  • PROM1 protein, human
  • Peptides
  • alpha-Fetoproteins
  • Granulocyte Colony-Stimulating Factor
  • Hepatocyte Growth Factor