Document Detail

A simple and economical route to generate functional hepatocyte-like cells from hESCs and their application in evaluating alcohol induced liver damage.
MedLine Citation:
PMID:  21956183     Owner:  NLM     Status:  Publisher    
The in vitro derived hepatocytes from human embryonic stem cells (hESC) is a promising tool to acquire improved knowledge of the cellular and molecular events underlying early human liver development under physiological and pathological conditions. Here we report a simple two-step protocol employing conditioned medium from human hepatocellular carcinoma cell line, HepG2 to generate functional hepatocyte-like cells from hESC. Immunocytochemistry, flow cytometry, quantitative RT-PCR and biochemical analyses revealed that the endodermal progenitors appeared as pockets in culture, and the cascade of genes associated with the formation of definitive endoderm (HNF-3β, SOX-17, DLX-5, CXCR4) was consistent and in concurrence with the up-regulation of the markers for hepatic progenitors (AFP, HNF-4α, CK-19, Albumin, AAT); followed by maturation into functional hepatocytes (TAT, TDO, G6P, CYP3A4, CYP7A1). We witnessed that the gene expression profile during this differentiation process recapitulated in vivo liver development demonstrating a gradual down regulation of extra embryonic endodermal markers (SOX-7, HNF-1β, SNAIL-1, LAMININ-1, CDX2); and the generated hepatic cells performed multiple liver functions. Since prenatal alcohol exposure is known to provoke irreversible abnormalities in the fetal cells and developing tissues; we exposed in vitro generated hepatocytes to ethanol found that ethanol treatment not only impairs the survival and proliferation, but also induces apoptosis and perturbs differentiation of progenitor cells into hepatocytes. This disruption was accompanied by alterations in the expression of genes and proteins involved in hepatogenesis. Our results provide new insights into the wider range of destruction caused by alcohol on the dynamic process of liver organogenesis. J. Cell. Biochem. © 2011 Wiley Periodicals, Inc.
Rajarshi Pal; Murali Krishna M; Anjan Kumar Das; Pawan Kumar Gupta; Ramesh Bhonde
Related Documents :
3684783 - Response of glandular versus basal rat ventral prostatic epithelial cells to androgen w...
11237123 - In vitro-activated human lupus t cells express normal estrogen receptor proteins which ...
12786493 - Cellular flow patterns and their evolutionary scenarios in three-dimensional rayleigh-b...
Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2011-9-28
Journal Detail:
Title:  Journal of cellular biochemistry     Volume:  -     ISSN:  1097-4644     ISO Abbreviation:  -     Publication Date:  2011 Sep 
Date Detail:
Created Date:  2011-9-29     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  8205768     Medline TA:  J Cell Biochem     Country:  -    
Other Details:
Languages:  ENG     Pagination:  -     Citation Subset:  -    
Copyright Information:
Copyright © 2011 Wiley Periodicals, Inc.
Manipal Institute of Regenerative Medicine, Manipal University Branch Campus, # 10 Service Road, Domlur Layout, Bangalore 560071, India.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Novel Oral Anticoagulants for VTE Prevention in Orthopedic Surgery: Overview of Phase 3 Trials.
Next Document:  Evolving treatment strategies for management of cardiorenal syndrome.