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World J Gastroenterol. Apr 28, 2007; 13(16): 2319-2323
Published online Apr 28, 2007. doi: 10.3748/wjg.v13.i16.2319
Characterization of hepatic progenitors from human fetal liver using CD34 as a hepatic progenitor marker
Parveen Nyamath, Ayesha Alvi, Aejaz Habeeb, Sanjeev Khosla, Aleem A Khan, CM Habibullah
Parveen Nyamath, Ayesha Alvi, Aejaz Habeeb, Aleem A Khan, CM Habibullah, Center for Liver Research and Diagnostics, Deccan College of Medical Sciences and Allied Hospitals, Kanchanbagh, Hyderabad-58, Andhra Pradesh, India
Sanjeev Khosla, Centre for DNA Fingerprinting and Diagnostics, Nacharam, Hyderabad 500072, India
Author contributions: All authors contributed equally to the work.
Supported by Department of Biotechnology, Government of India
Correspondence to: Aleem Ahmed Khan, Centre for Liver Research and Diagnostics, Deccan College of Medical Sciences, Kanchanbagh 500058, Hyderabad-A.P,India. aleem_a_khan@rediffmail.com
Telephone: +91-40-23432954
Received: May 25, 2006
Revised: December 3, 2006
Accepted: January 30, 2007
Published online: April 28, 2007
Abstract

AIM: To enrich putative hepatic progenitors from the developing human fetal liver using CD34 as a marker.

METHODS: Aborted fetuses of 13-20 wk were used for the isolation of liver cells. The cells were labeled with anti CD34; a marker used for isolating progenitor population and the cells were sorted using magnetic cell sorting. The positive fractions of cells were assessed for specific hepatic markers. Further, these cells were cultured in vitro for long term investigation.

RESULTS: Flow cytometric and immunocytochemical analysis for alphafetoprotein (AFP) showed that the majority of the enriched CD34 positive cells were positive for AFP. Furthermore, these enriched cells proliferated in the long term and maintained hepatic characteristics in in vitro culture.

CONCLUSION: The study shows that aborted human fetal liver is a potential source for isolation of hepatic progenitors for clinical applications. The study also demonstrates that CD34 can be a good marker for the enrichment of progenitor populations.

Keywords: Progenitor cells; Fetal liver; Magnetic cell sorting; Flow cytometry; Immunohistochemistry