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Isolation and Enrichment of Liver Progenitor Subsets Identified by a Novel Surface Marker Combination
Published on: February 18, 2017
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Novel surface markers directed against adult human gallbladder
Feorillo H Galivo1, Craig Dorrell1, Maria T Grompe1
1Oregon Stem Cell Center, Papé Family Pediatric Research Institute, Department of Pediatrics, Oregon Health & Science University, 3181 SW Sam Jackson Park Road, Portland, OR 97239, USA.
Stem Cell Research
|June 17, 2015
Summary
Researchers developed new antibodies to identify diverse human gallbladder cell types, revealing potential roles in bile physiology and cancer. These antibodies also show promise as biomarkers for gallbladder carcinoma.
Area of Science:
- Cell Biology
- Immunology
- Gastroenterology
Background:
- The human gallbladder harbors diverse cell populations crucial for bile physiology.
- Characterizing these cell subsets is essential for understanding gallbladder function and disease.
Purpose of the Study:
- To develop novel monoclonal antibodies for isolating and characterizing human gallbladder cell subsets.
- To investigate the potential functional properties and biomarker utility of these cell subsets.
Main Methods:
- Generation of cell surface-reactive monoclonal antibodies against extrahepatic biliary cells.
- Isolation of gallbladder cell subpopulations using fluorescence-activated cell sorting.
- Classification of cell subsets via gene expression profiling (e.g., PDX1(+)SOX9(+)).
Main Results:
- Eleven antigenically distinct human gallbladder cell subpopulations were isolated.
- Subsets were classified as epithelial, mesenchymal, and pancreatobiliary.
- Three novel monoclonal antibodies showed differential labeling in gallbladder carcinoma compared to normal tissue.
Conclusions:
- Novel monoclonal antibodies enable the identification and characterization of diverse human gallbladder cell subsets.
- These cell subsets may possess distinct functional properties related to bile physiology, renewal, and plasticity.
- The developed antibodies serve as potential biomarkers for human gallbladder carcinoma.

