Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/96562
Title: Vasculogenic and osteogenesis-enhancing potential of human umbilical cord blood endothelial colony-forming cells
Authors: Lee, Eddy S. M.
Mattar, Citra N. Z.
Medina, Reinhold J.
Kamm, Roger D.
Fisk, Nicholas M.
Liu, Yuchun
Teoh, Swee-Hin
Chong, Mark Seow Khoon
Randhawa, Nau'shil Kaur
Zhang, Zhi-yong
Choolani, Mahesh
Chan, Jerry Kok Yen
Issue Date: 2012
Source: Liu, Y., Teoh, S.-H., Chong, M. S. K., Lee, E. S. M., Mattar, C. N. Z., Randhawa, N. K., et al. (2012). Vasculogenic and osteogenesis-enhancing potential of human umbilical cord blood endothelial colony-forming cells. STEM CELLS, 30(9), 1911-1924.
Series/Report no.: STEM CELLS
Abstract: Umbilical cord blood-derived endothelial colony-forming cells (UCB-ECFC) show utility in neovascularization, but their contribution to osteogenesis has not been defined. Cocultures of UCB-ECFC with human fetal-mesenchymal stem cells (hfMSC) resulted in earlier induction of alkaline phosphatase (ALP) (Day 7 vs. 10) and increased mineralization (1.9×; p < .001) compared to hfMSC monocultures. This effect was mediated through soluble factors in ECFC-conditioned media, leading to 1.8–2.2× higher ALP levels and a 1.4–1.5× increase in calcium deposition (p < .01) in a dose-dependent manner. Transcriptomic and protein array studies demonstrated high basal levels of osteogenic (BMPs and TGF-βs) and angiogenic (VEGF and angiopoietins) regulators. Comparison of defined UCB and adult peripheral blood ECFC showed higher osteogenic and angiogenic gene expression in UCB-ECFC. Subcutaneous implantation of UCB-ECFC with hfMSC in immunodeficient mice resulted in the formation of chimeric human vessels, with a 2.2-fold increase in host neovascularization compared to hfMSC-only implants (p = .001). We conclude that this study shows that UCB-ECFC have potential in therapeutic angiogenesis and osteogenic applications in conjunction with MSC. We speculate that UCB-ECFC play an important role in skeletal and vascular development during perinatal development but less so in later life when expression of key osteogenesis and angiogenesis genes in ECFC is lower.
URI: https://hdl.handle.net/10356/96562
http://hdl.handle.net/10220/10314
ISSN: 1549-4918
DOI: 10.1002/stem.1164
Rights: © 2012 AlphaMed Press.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:SCBE Journal Articles

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