Efficient generation of functional hepatocyte‐like cells from menstrual blood‐derived stem cells. (18th March 2013)

• Record Type: Journal Article
• Authors: Khanjani, Sayeh; Khanmohammadi, Manijeh; Zarnani, Amir Hassan; Talebi, Saeed; Edalatkhah, Haleh; Eghtesad, Saman; Nikokar, Iraj; Kazemnejad, Somaieh
• Is Part Of: Journal of tissue engineering and regenerative medicine. Volume 9:Number 11(2015)
• Page Start: E124
• Page End: E134
• Publication Date: 2013-03-18
• Subjects: menstrual blood -- stem cell -- hepatocyte -- differentiation; Tissue engineering -- Periodicals; Regeneration (Biology) -- Periodicals; 610.28
• DOI: 10.1002/term.1715
• Languages: English
• ISSNs: 1932-6254

Abstract

Abstract: In recent years, the advantages of menstrual blood‐derived stem cells (MenSCs), such as minimal ethical considerations, easy access and high proliferative ability, have inspired scientists to investigate the potential of MenSCs in cell therapy of different diseases. In order to characterize the potency of these cells for future cell therapy of liver diseases, we examined the potential of MenSCs to differentiate into hepatocytes, using different protocols. First, the immunophenotyping properties and potential of MenSCs to differentiate into osteoblasts, adipocytes and chondrocytes were evaluated. Thereafter, the differentiation protocols developed by two concentrations of hepatocyte growth factor (HGF) and oncostatin M (OSM), in combination with other components in serum‐supplemented or serum‐free culture media, were also investigated. The sequential differentiation was monitored by real‐time PCR, immunostaining and functional assays. Our primary data revealed that the isolated MenSCs exhibited mesenchymal stem cell markers in parallel to OCT‐4 as an embryonic marker. Regardless of differentiation procedures, the developed cells expressed mature hepatocyte markers, such as albumin, tyrosine aminotransferase and cytokeratin‐18 at the mRNA and protein levels. They also showed functional properties of hepatocytes, including albumin secretion, glycogen storage and cytochrome P450 7A1 expression. However, the degree of differentiation was dependent on the concentrations of HGF and OSM. Indeed, omission of serum during the differentiation process caused typical improvement in hepatocyte‐specific functions. This study is a novel report demonstrating the differentiation potential of MenSCs into hepatocyte‐like cells. We recommend a complementary serum‐free differentiation protocol for enrichment of in vitro production of functional MenSC‐derived hepatocyte‐like cells that could lead to a major step toward applied stem cell therapy of chronic liver diseases. Copyright © 2013 John Wiley & Sons, Ltd.