Endothelial cells influence the osteogenic potential of bone marrow stromal cells

<p>Abstract</p> <p>Background</p> <p>Improved understanding of the interactions between bone cells and endothelial cells involved in osteogenesis should aid the development of new strategies for bone tissue engineering. The aim of the present study was to determine whet...

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Main Authors: Arvidson Kristina, Hellem Sølve, Xing Zhe, Xue Ying, Mustafa Kamal
Format: Article
Language:English
Published: BMC 2009-11-01
Series:BioMedical Engineering OnLine
Online Access:http://www.biomedical-engineering-online.com/content/8/1/34
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spelling doaj-260d7ba291b6498a96c9ea66f40bad112020-11-24T21:44:39ZengBMCBioMedical Engineering OnLine1475-925X2009-11-01813410.1186/1475-925X-8-34Endothelial cells influence the osteogenic potential of bone marrow stromal cellsArvidson KristinaHellem SølveXing ZheXue YingMustafa Kamal<p>Abstract</p> <p>Background</p> <p>Improved understanding of the interactions between bone cells and endothelial cells involved in osteogenesis should aid the development of new strategies for bone tissue engineering. The aim of the present study was to determine whether direct communication between bone marrow stromal cells (MSC) and human umbilical vein endothelial cells (EC) could influence the osteogenic potential of MSC in osteogenic factor-free medium.</p> <p>Methods</p> <p>After adding EC to MSC in a direct-contact system, cell viability and morphology were investigated with the WST assay and immnostaining. The effects on osteogenic differentiation of adding EC to MSC was systematically tested by the using Superarray assay and results were confirmed with real-time PCR.</p> <p>Results</p> <p>Five days after the addition of EC to MSC in a ratio of 1:5 (EC/MSC) significant increases in cell proliferation and cellular bridges between the two cell types were detected, as well as increased mRNA expression of alkaline phosphatase (ALP). This effect was greater than that seen with addition of osteogenic factors such as dexamethasone, ascorbic acid and β-glycerophosphate to the culture medium. The expression of transcription factor Runx2 was enhanced in MSC incubated with osteogenic stimulatory medium, but was not influenced by induction with EC. The expression of Collagen type I was not influenced by EC but the cells grown in the osteogenic factor-free medium exhibited higher expression than those cultured with osteogenic stimulatory medium.</p> <p>Conclusion</p> <p>These results show that co-culturing of EC and MSC for 5 days influences osteogenic differentiation of MSC, an effect that might be independent of Runx2, and enhances the production of ALP by MSC.</p> http://www.biomedical-engineering-online.com/content/8/1/34
collection DOAJ
language English
format Article
sources DOAJ
author Arvidson Kristina
Hellem Sølve
Xing Zhe
Xue Ying
Mustafa Kamal
spellingShingle Arvidson Kristina
Hellem Sølve
Xing Zhe
Xue Ying
Mustafa Kamal
Endothelial cells influence the osteogenic potential of bone marrow stromal cells
BioMedical Engineering OnLine
author_facet Arvidson Kristina
Hellem Sølve
Xing Zhe
Xue Ying
Mustafa Kamal
author_sort Arvidson Kristina
title Endothelial cells influence the osteogenic potential of bone marrow stromal cells
title_short Endothelial cells influence the osteogenic potential of bone marrow stromal cells
title_full Endothelial cells influence the osteogenic potential of bone marrow stromal cells
title_fullStr Endothelial cells influence the osteogenic potential of bone marrow stromal cells
title_full_unstemmed Endothelial cells influence the osteogenic potential of bone marrow stromal cells
title_sort endothelial cells influence the osteogenic potential of bone marrow stromal cells
publisher BMC
series BioMedical Engineering OnLine
issn 1475-925X
publishDate 2009-11-01
description <p>Abstract</p> <p>Background</p> <p>Improved understanding of the interactions between bone cells and endothelial cells involved in osteogenesis should aid the development of new strategies for bone tissue engineering. The aim of the present study was to determine whether direct communication between bone marrow stromal cells (MSC) and human umbilical vein endothelial cells (EC) could influence the osteogenic potential of MSC in osteogenic factor-free medium.</p> <p>Methods</p> <p>After adding EC to MSC in a direct-contact system, cell viability and morphology were investigated with the WST assay and immnostaining. The effects on osteogenic differentiation of adding EC to MSC was systematically tested by the using Superarray assay and results were confirmed with real-time PCR.</p> <p>Results</p> <p>Five days after the addition of EC to MSC in a ratio of 1:5 (EC/MSC) significant increases in cell proliferation and cellular bridges between the two cell types were detected, as well as increased mRNA expression of alkaline phosphatase (ALP). This effect was greater than that seen with addition of osteogenic factors such as dexamethasone, ascorbic acid and β-glycerophosphate to the culture medium. The expression of transcription factor Runx2 was enhanced in MSC incubated with osteogenic stimulatory medium, but was not influenced by induction with EC. The expression of Collagen type I was not influenced by EC but the cells grown in the osteogenic factor-free medium exhibited higher expression than those cultured with osteogenic stimulatory medium.</p> <p>Conclusion</p> <p>These results show that co-culturing of EC and MSC for 5 days influences osteogenic differentiation of MSC, an effect that might be independent of Runx2, and enhances the production of ALP by MSC.</p>
url http://www.biomedical-engineering-online.com/content/8/1/34
work_keys_str_mv AT arvidsonkristina endothelialcellsinfluencetheosteogenicpotentialofbonemarrowstromalcells
AT hellemsølve endothelialcellsinfluencetheosteogenicpotentialofbonemarrowstromalcells
AT xingzhe endothelialcellsinfluencetheosteogenicpotentialofbonemarrowstromalcells
AT xueying endothelialcellsinfluencetheosteogenicpotentialofbonemarrowstromalcells
AT mustafakamal endothelialcellsinfluencetheosteogenicpotentialofbonemarrowstromalcells
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