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http://hdl.handle.net/1942/33999
Title: | In vitro hepatic differentiation of human bone marrow mesenchymal stem cells under differential exposure to liver-specific factors | Authors: | Chivu, M Dima, SO STANCU, Ilie Cosmin Dobrea, C Uscatescu, V Necula, LG Bleotu, C Tanase, C Albulescu, R Ardeleanu, C Popescu, I |
Issue Date: | 2009 | Publisher: | ELSEVIER SCIENCE INC | Source: | Translational Research, 154 (3) , p. 122 -132 | Abstract: | Recent findings demonstrated that stem cells could be harvested from a patient and used to repair his or her own damaged liver. Additionally, stem cells may be manipulated in vitro to induce hepatic differentiation. The current study aims to determine the differentiation efficacy of various liver-specific factors (hepatocyte growth factor, Insulin-Transferrin-Selenium, dexamethasone, and nicotinamide) used for stem cell differentiation into hepatocyte-like cells. Human mesenchymal stem cells were exposed to different media containing these compounds added individually or in various combinations. Hepatic differentiation was assessed via quantitative reverse transcription-polymerase chain reaction and immunocytochemical staining for stemness or liver-specific genes and proteins, including albumin, cytokeratins 18 and 19, HepPar-1, alpha-fetoprotein, and nestin. In addition, functional tests for glycogen storage, urea production, glucose, and albumin synthesis were also performed. The expression profiles of albumin, alpha-fetoprotein, and cytokeratin 19 demonstrated that when hepatocyte growth factor, nicotinamide, or dexamethasone were added individually, incomplete hepatocyte differentiation was achieved; the obtained cell populations contained progenitors that expressed both hepatic (albumin) and biliary (cytokeratin 19) markers, as well as alpha-fetoprotein. Hepatocyte growth factor and nicotinamide were the factors with the most hepatogenic potential. When all factors were added to the culture, cells exhibited features that closely resembled human adult hepatocytes as determined by their gene expression patterns (albumin, HepPar-1, and alpha-fetoprotein, but not cytokeratin 19) and functional testing. These cells with hepatic function may become important tools for liver transplant procedures, liver development studies, and pharmacologic research. (Translational Research 2009;154:122-132) | Document URI: | http://hdl.handle.net/1942/33999 | ISSN: | 1931-5244 | e-ISSN: | 1878-1810 | DOI: | 10.1016/j.trsl.2009.05.007 | ISI #: | WOS:000269235600003 | Category: | A1 | Type: | Journal Contribution |
Appears in Collections: | Research publications |
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1-s2.0-S1931524409001765-main.pdf Restricted Access | Published version | 1.95 MB | Adobe PDF | View/Open Request a copy |
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