Source:http://linkedlifedata.com/resource/pubmed/id/17518657
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
10
|
pubmed:dateCreated |
2007-5-23
|
pubmed:abstractText |
Angiogenesis plays an important role in bone development, repair, and remodelling. Neovascularization is furthermore a crucial step in bone tissue engineering because implantation of voluminous grafts without sufficient vascularity results in hypoxic cell death of the engineered tissue. We have previously described a co-cultivation system of human primary osteoblasts and human primary endothelial cells that was developed to improve neovascularization in bone tissue-engineering applications. In our present study, we have performed complementary deoxyribonucleic acid microarray analysis to analyze putative changes in osteoblastic gene expression upon co-cultivation of osteoblasts and endothelial cells. Transcriptional profiling revealed upregulation of 79 genes and downregulation of 62 genes in osteoblasts after co-cultivation with endothelial cells. To verify the microarray data, quantitative real-time reverse transcriptase polymerase chain reaction was carried out on selected genes. The expression of the platelet-derived growth factor receptor alpha gene in osteoblasts was analyzed in more detail, revealing that a cell contact-dependent mechanism, and not paracrine-acting diffusible factors, mediates the downregulation of this receptor in osteoblasts upon co-cultivation with endothelial cells. In summary, the data demonstrate complex gene-regulation mechanisms between endothelial cells and osteoblasts that are likely to play a role in bone morphogenesis.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Oct
|
pubmed:issn |
1076-3279
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
12
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
2889-903
|
pubmed:dateRevised |
2009-11-19
|
pubmed:meshHeading |
pubmed-meshheading:17518657-Angiogenic Proteins,
pubmed-meshheading:17518657-Cell Adhesion,
pubmed-meshheading:17518657-Cell Differentiation,
pubmed-meshheading:17518657-Cells, Cultured,
pubmed-meshheading:17518657-Coculture Techniques,
pubmed-meshheading:17518657-Drug Delivery Systems,
pubmed-meshheading:17518657-Endothelial Cells,
pubmed-meshheading:17518657-Gene Expression Profiling,
pubmed-meshheading:17518657-Gene Expression Regulation,
pubmed-meshheading:17518657-Humans,
pubmed-meshheading:17518657-Neovascularization, Physiologic,
pubmed-meshheading:17518657-Osteoblasts,
pubmed-meshheading:17518657-Osteogenesis,
pubmed-meshheading:17518657-Receptor, Platelet-Derived Growth Factor alpha,
pubmed-meshheading:17518657-Tissue Engineering
|
pubmed:year |
2006
|
pubmed:articleTitle |
Gene expression profiling reveals platelet-derived growth factor receptor alpha as a target of cell contact-dependent gene regulation in an endothelial cell-osteoblast co-culture model.
|
pubmed:affiliation |
Department of Plastic and Hand Surgery, University of Freiburg Medical Center, Freiburg, Germany. finkenzeller@ch11.ukl.uni-freiburg.de
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|