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Open Access Methodology article

A novel early precursor cell population from rat bone marrow promotes angiogenesis in vitro

Andreas Brandl, Quan Yuan, Anja M Boos, Justus P Beier, Andreas Arkudas, Ulrich Kneser, Raymund E Horch and Oliver Bleiziffer*

Author Affiliations

Department of Plastic and Hand Surgery, Hospital of Erlangen, Friedrich-Alexander-University of Erlangen-Nuremberg, Krankenhausstrasse 12, Erlangen 91054, Germany

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BMC Cell Biology 2014, 15:12  doi:10.1186/1471-2121-15-12

Published: 26 March 2014

Abstract

Background

Some studies demonstrated therapeutic angiogenesis attributable to the effects of endothelial progenitor cells (EPC), others have reported disappointing results. This may be due to the fact that EPC populations used in these contradictory studies were selected and defined by highly variable and differing experimental protocols. Indeed, the isolation and reliable characterization of ex vivo differentiated EPC raises considerable problems due to the fact there is no biomarker currently available to specifically identify EPC exclusively. On the other hand traditional differentiation of primary immature bone marrow cells towards the endothelial lineage is a time-consuming process of up to 5 weeks. To circumvent these shortcomings, we herein describe a facile method to isolate and enrich a primary cell population from rat bone marrow, combining differential attachment methodology with cell sorting technology.

Results

The combination of these techniques enabled us to obtain a pure population of early endothelial precursor cells that show homogenous upregulation of CD31 and VEGF-R2 and that are positive for CD146. These cells exhibited typical sprouting on Matrigel™. Additionally, this population displayed endothelial tube formation when resuspended in Matrigel™ as well as in fibrin glue, demonstrating its functional angiogenic capacity. Moreover, these cells stained positive for DiI-ac-LDL and FITC-UEA, two markers that are commonly considered to stain differentiating EPCs. Based upon these observations in this study we describe a novel and time-saving method for obtaining a pure endothelial precursor cell population as early as 2–3 weeks post isolation that exhibits endothelial abilities in vitro and which still might have retained its early endothelial lineage properties.

Conclusion

The rapid isolation and the high angiogenic potential of these syngeneic cells might facilitate and accelerate the pre-vascularization of transplanted tissues and organs also in a human setting in the future.

Keywords:
Angiogenesis; Endothelial progenitor cells (EPC); Tissue engineering; Bone marrow; Rat