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Abstract
Objective: Fetal placental mesenchymal stem cells (fPMSCs) have shown promising cell therapy potentials. However, their genetic and epigenetic stability during in vitro propagation has not been well studied. We thus interrogated the methylation alterations and tumorigenicity of fPMSCs after in vitro expansion using serum-free medium.
Research design and methods: The properties of fPMSCs cultured in a serum-free medium at passage 3 and passage 8 were ascertained by determining their MSC markers, proliferative capacity, chromosomal stability, activity of global DNA methyltransferases and methylation profile. Their potential of malignant transformation was also evaluated in a severe combined immunodeficiency (SCID) murine model.
Results: The fPMSCs could maintain their MSC characteristics but quickly reached a senescent state of proliferation during in vitro expansion. 246 genes with differential DNA methylation of promoters were identified, along with a significantly downregulated global DNA methyltransferase activity. The genes associated with aging and tumorigenesis had a significantly demethylated tendency over in vitro propagation. However, the deposition of epigenetic alterations did not translate into malignant transformation in SCID mice.
Conclusion: The fPMSCs cultured in serum-free medium have a tendency to deposit methylation modifications over in vitro expansion, therefore the detection of genetic and/or epigenetic alterations is necessary for fPMSCs before they are employed for clinical uses.
Acknowledgment
J Wang, Y Li and Y Yang conceived and designed the experiments, drafted the manuscript; Y Zhu, X Song, J Wang, T Yang, H Ma, G Zhang and L Wang collected samples, performed experiments and acquired data and drafted the manuscript; Y Zhu analyzed the data and revised the manuscript; X Liu and WC Cho interpreted data and critically revised the manuscript. All authors read and approved the final version of the manuscript.
Declaration of interest
This work was supported in part by a grant of Ningxia Key Science and Technologies R & D program for Jun Wei (2011). The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed.