Identification of a candidate stem cell in human gallbladder

Stem Cell Res. 2015 May;14(3):258-69. doi: 10.1016/j.scr.2014.12.003. Epub 2015 Feb 7.

Abstract

There are currently no reports of identification of stem cells in human gallbladder. The differences between human gallbladder and intrahepatic bile duct (IHBD) cells have also not been explored. The goals of this study were to evaluate if human fetal gallbladder contains a candidate stem cell population and if fetal gallbladder cells are distinct from fetal IHBD cells. We found that EpCAM+CD44+CD13+ cells represent the cell population most enriched for clonal self-renewal from primary gallbladder. Primary EpCAM+CD44+CD13+ cells gave rise to EpCAM+CD44+CD13+ and EpCAM+CD44+CD13- cells in vitro, and gallbladder cells expanded in vitro exhibited short-term engraftment in vivo. Last, we found that CD13, CD227, CD66, CD26 and CD49b were differentially expressed between gallbladder and IHBD cells cultured in vitro indicating clear phenotypic differences between the two cell populations. Microarray analyses of expanded cultures confirmed that both cell types have unique transcriptional profiles with predicted functional differences in lipid, carbohydrate, nucleic acid and drug metabolism. In conclusion, we have isolated a distinct clonogenic population of epithelial cells from primary human fetal gallbladder with stem cell characteristics and found it to be unique compared to IHBD cells.

MeSH terms

  • Antigens, Neoplasm / genetics
  • Antigens, Neoplasm / metabolism
  • Bile Ducts, Intrahepatic / cytology*
  • Biomarkers / metabolism
  • CD13 Antigens / metabolism
  • Cell Adhesion Molecules / genetics
  • Cell Adhesion Molecules / metabolism
  • Cell Differentiation
  • Cell Self Renewal
  • Cells, Cultured
  • Epithelial Cell Adhesion Molecule
  • Gallbladder / cytology*
  • Gallbladder / embryology
  • Gene Expression Profiling
  • Humans
  • Hyaluronan Receptors / metabolism
  • Oligonucleotide Array Sequence Analysis
  • Phenotype
  • Stem Cells / cytology*

Substances

  • Antigens, Neoplasm
  • Biomarkers
  • Cell Adhesion Molecules
  • EPCAM protein, human
  • Epithelial Cell Adhesion Molecule
  • Hyaluronan Receptors
  • CD13 Antigens