Construction and characterization of human bone marrow-derived mesenchymal stem cells by overexpressing human telomerase gene

Authors

  • Chattana Tiyasoponjit Center of Excellence for Stem Cell Research, Thammasat University, Pathumthani, Thailand
  • Kantpitchar Supraditaporn Siriraj Center of Excellence for Stem Cell Research, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand
  • Phatchanat Klaihmon Siriraj Center of Excellence for Stem Cell Research, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand
  • Sirikul Manochantr Center of Excellence for Stem Cell Research, Thammasat University, Pathumthani, Thailand and Division of Cell Biology, Faculty of Medicine, Thammasat University, Pathumthani, Thailand
  • Chairat Tantrawatpan Center of Excellence for Stem Cell Research, Thammasat University, Pathumthani, Thailand and Division of Cell Biology, Faculty of Medicine, Thammasat University, Pathumthani, Thailand
  • Duangrat Tantikanlayaporn Center of Excellence for Stem Cell Research, Thammasat University, Pathumthani, Thailand and Division of Cell Biology, Faculty of Medicine, Thammasat University, Pathumthani, Thailand
  • Pakpoom Kheolamai Center of Excellence for Stem Cell Research, Thammasat University, Pathumthani, Thailand and Division of Cell Biology, Faculty of Medicine, Thammasat University, Pathumthani, Thailand

Keywords:

human mesenchymal stem cells, bone marrow, telomerase

Abstract

Introduction: Currently, bone marrow-derived human mesenchymal stem cells (BM-hMSCs) have been considered a standard source of hMSCs for research and clinical applications. However, the number of BM-hMSCs in bone marrow decline with age and the isolated BM-hMSCs have limited proliferative capacity which are major hurdles for most research and clinical uses which require large number of cells, therefore development of the novel technique for enhancing BM-hMSC expansion in culture is critical.

Methods: This study, the genetic-engineering technique was employed to enhance the expression level of human telomerase gene (hTERT) in BM-hMSCs (hTERT-BM-hMSCs). The hTERT-BM-hMSCs were characterized in term of their morphology, gene expression profile, as well as their osteogenic and adipogenic differentiation potentials in comparison to the non-transfected BM-hMSCs (NT-BM-hMSCs)

Results: The hTERT-BM-hMSCs could be expanded in culture for a longer period of time compared with their non-transfected counterparts and retained the typical characteristics and properties of BM-hMSCs, such as morphology, surface marker expression profile, adipogenic and osteogenic differentiation capacity.

Conclusion: The hTERT overexpression enhanced the expansion potential of BM-hMSCs without altering their properties. The hTERT-BM-hMSCs established in this study is beneficial for genetically manipulation of BM-hMSCs which is usually difficult to perform due to their limited proliferative capability.

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Published

2019-06-21

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Section

Original Articles