Journal
BIOMATERIALS
Volume 30, Issue 7, Pages 1329-1338Publisher
ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2008.11.028
Keywords
Angiogenesis; Bone tissue engineering; Co-culture; Image analysis; Endothelial progenitor cells
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For successful bone regeneration tissue engineered bone constructs combining both aspects, namely a high osteogenic potential and a rapid connection to the vascular network are needed. In this study we assessed the formation of pre-vascular structures by human outgrowth endothelial cells (OEC) from progenitors in the peripheral blood and the osteogenic differentiation of primary human osteoblasts (pOB) on micrometric silk fibroin scaffolds. The rational was to gain more insight into the dynamic processes involved ill the differentiation and functionality of both cell types depending on culture time in vitro. Vascular tube formation by OEC was assessed quantitatively at one and 4 weeks of culture. In parallel, we assessed the temporal changes in cell ratios by flow cytometry and in the marker profiles of endothelial and osteogenic markers by quantitative real-tinge PCR. In terms of OEC. we observed an increase ill tube length, tube area, number of nodes and number of vascular meshes within a culture period of 4 weeks, but a decrease in endothelial markers ill real-time PCR. At the same time early osteogenic markers were downregulated, while marker expression associated with progress ng mineralized matrix was upregulated in later stages of the culture. In addition, deposition of matrix components, such as collagen type I, known as a pro-angiogenic substrate for endothelial cells, appeared to increase with time indicated by immunohistochemistry. In summary, the study suggests a progressing Maturation of the tissue construct with culture time which seems to be not effected by Culture conditions mainly designed for outgrowth endothelial cells. (c) 2008 Elsevier Ltd. All rights reserved.
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