Osteoprotegerin Induces CD34+ Differentiation in Endothelial Progenitor Cells
Endothelial progenitor cells (EPCs) are the main hypothetical cells that could give rise to vessels and in particular one subtype isolated from peripheral or cord bloods: endothelial colony forming cells (ECFCs). These ECFCs are clonogenic precursors committed to endothelial lineage and have robust...
Saved in:
Published in | Frontiers in medicine Vol. 5; p. 331 |
---|---|
Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers media
27.11.2018
Frontiers Media S.A |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Endothelial progenitor cells (EPCs) are the main hypothetical cells that could give rise to vessels and in particular one subtype isolated from peripheral or cord bloods: endothelial colony forming cells (ECFCs). These ECFCs are clonogenic precursors committed to endothelial lineage and have robust vasculogenic properties. However, their low number and poor expansion properties when isolated from human adult bloods, currently limit their use as an autologous cell therapy product. We previously reported that osteoprotegerin (OPG), a well-characterized regulator of bone metabolism, contributes to ischemic tissue revascularization, tumor growth
, and potentiates ECFCs proangiogenic properties through the secretion of SDF-1. The current study investigated the role of OPG in ECFCs differentiation and expansion from cord blood CD34
cells. OPG increased the number of ECFCs after endothelial differentiation of CD34
cells, enhancing the time of EPCs colonies initial appearance and the growth kinetic of endothelial cell progeny. OPG-exposed ECFCs expressed higher levels of CD34
compared to control ECFCs. In conclusion, our findings provide novel insights into OPG in regulation of CD34
progenitor cells. These results give new opportunities for
expansion of human ECFCs using OPG as a cell culture component for future ECFC product manufacture according to GMP. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 PMCID: PMC6277572 Edited by: Ondrej Viklicky, Institute for Clinical and Experimental Medicine (IKEM), Czechia Reviewed by: Marian Klinger, Opole University, Poland; Tomomi Toubai, Yamagata University, Japan This article was submitted to Translational Medicine, a section of the journal Frontiers in Medicine |
ISSN: | 2296-858X 2296-858X |
DOI: | 10.3389/fmed.2018.00331 |