Publication: Proteomic profiles of mesenchymal stem cells induced by a liver differentiation protocol
Issued Date
2010-12-01
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14220067
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2-s2.0-78650983674
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Mahidol University
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SCOPUS
Bibliographic Citation
International Journal of Molecular Sciences. Vol.11, No.12 (2010), 4905-4915
Suggested Citation
Kawin Leelawat, Siriluck Narong, Suthidarak Chaijan, Khanit Sa-Ngiamsuntorn, Sinee Disthabanchong, Adisak Wongkajornsilp, Suradej Hongeng Proteomic profiles of mesenchymal stem cells induced by a liver differentiation protocol. International Journal of Molecular Sciences. Vol.11, No.12 (2010), 4905-4915. doi:10.3390/ijms11124905 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/28588
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Title
Proteomic profiles of mesenchymal stem cells induced by a liver differentiation protocol
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Abstract
The replacement of disease hepatocytes and the stimulation of endogenous or exogenous regeneration by human mesenchymal stem cells (MSCs) are promising candidates for liver-directed cell therapy. In this study, we isolated MSCs from adult bone marrow by plastic adhesion and induced differentiation with a liver differentiation protocol. Western blot analyses were used to assess the expression of liver-specific markers. Next, MSC-specific proteins were analyzed with two-dimensional (2D) gel electrophoresis and peptide mass fingerprinting matrix-assisted laser desorption/ionization (MALDI)-time of flight (TOF)-mass spectrometry (MS). To confirm the results from the proteomic study, semi-quantitative reverse transcription-polymerase chain reaction (RT-PCR) analyses were performed. We demonstrated that MSCs treated with the liver differentiation protocol expressed significantly more albumin, CK19 and CK20, than did undifferentiated cells. In addition the results of proteomic study demonstrated increases expression of FEM1B, PSMC2 and disulfide-isomerase A3 in MSCs treated with the liver differentiation protocol. These results from proteomic profiling will not only provide insight into the global responses of MSCs to hepatocyte differentiation, but will also lead to in-depth studies on the mechanisms of proteomic changes in MSCs. © 2010 by the authors.