Dynamic processes involved in the pre-vascularization of silk fibroin constructs for bone regeneration using outgrowth endothelial cells

被引:132
作者
Fuchs, Sabine [1 ]
Jiang, Xin [1 ]
Schmidt, Harald [2 ]
Dohle, Eva [1 ]
Ghanaati, Shahram [1 ]
Orth, Carina [1 ]
Hofmann, Alexander [3 ]
Motta, Antonella [4 ]
Migliaresi, Claudio [4 ]
Kirkpatrick, Charles J. [1 ]
机构
[1] Johannes Gutenberg Univ Mainz, Inst Pathol, D-55101 Mainz, Germany
[2] MetaPhysiol, D-35270 Essenheim, Germany
[3] Johannes Gutenberg Univ Mainz, Dept Trauma Surg, D-55101 Mainz, Germany
[4] Univ Trento, Dept Mat Engn & Ind Technol, Trento, Italy
关键词
Angiogenesis; Bone tissue engineering; Co-culture; Image analysis; Endothelial progenitor cells; HUMAN PERIPHERAL-BLOOD; MESENCHYMAL STEM-CELLS; IN-VITRO; LUMEN FORMATION; MESSENGER-RNAS; DIFFERENTIATION; GROWTH; ANGIOGENESIS; EXPRESSION; OSTEOBLASTS;
D O I
10.1016/j.biomaterials.2008.11.028
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
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.
引用
收藏
页码:1329 / 1338
页数:10
相关论文
共 44 条
[1]  
AU P, 2008, BLOOD
[2]   Advances in the osteoblast lineage [J].
Aubin, JE .
BIOCHEMISTRY AND CELL BIOLOGY, 1998, 76 (06) :899-910
[3]   Functionality of endothelial cells on silk fibroin nets: Comparative study of micro- and nanometric fibre size [J].
Bondar, Borys ;
Fuchs, Sabine ;
Motta, Antonella ;
Migliaresi, Claudio ;
Kirkpatrick, Charles J. .
BIOMATERIALS, 2008, 29 (05) :561-572
[4]   Distinct patterns of microvascular endothelial cell morphology are determined by extracellular matrix composition [J].
Dye, JF ;
Lawrence, L ;
Linge, C ;
Leach, L ;
Firth, JA ;
Clark, P .
ENDOTHELIUM-JOURNAL OF ENDOTHELIAL CELL RESEARCH, 2004, 11 (3-4) :151-167
[5]   Endothelial cell apoptosis during glomerular capillary lumen formation in vivo [J].
Fierlbeck, W ;
Liu, AL ;
Coyle, R ;
Ballermann, BJ .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2003, 14 (05) :1349-1354
[6]  
FINKENZELLER G, 2006, TISSUE ENG
[7]  
FUCHS S, 2006, CELL TISSUE RES, P1
[8]   Microvessel-like structures from outgrowth endothelial cells from human peripheral blood in 2-dimensional and 3-dimensional co-cultures with osteoblastic lineage cells [J].
Fuchs, Sabine ;
Hofmann, Alexander ;
Kirkpatrick, C. James .
TISSUE ENGINEERING, 2007, 13 (10) :2577-2588
[9]   Outgrowth endothelial cells isolated and expanded from human peripheral blood progenitor cells cells for endothelialization as a potential source of autologous of silk fibroin biomaterials [J].
Fuchs, Sabine ;
Motta, Antonella ;
Migliaresi, Claudio ;
Kirkpatrick, Charles James .
BIOMATERIALS, 2006, 27 (31) :5399-5408
[10]   Contribution of outgrowth endothelial cells from human peripheral blood on in vivo vascularization of bone tissue engineered constructs based on starch polycaprolactone scaffolds [J].
Fuchs, Sabine ;
Ghanaati, Shahram ;
Orth, Carina ;
Barbeck, Mike ;
Kolbe, Marten ;
Hofmann, Alexander ;
Eblenkamp, Markus ;
Gomes, Manuela ;
Reis, Rui L. ;
Kirkpatrick, Charles J. .
BIOMATERIALS, 2009, 30 (04) :526-534