间质细胞
细胞生物学
脂肪组织
肝细胞生长因子
化学
体外
骨髓
川地34
脐静脉
干细胞
免疫学
生物
癌症研究
生物化学
受体
作者
Femke Verseijden,Sandra J. Posthumus-van Sluijs,P. Pavljasevic,Stefan O.P. Hofer,Gerjo J.V.M. van Osch,Eric Farrell
出处
期刊:Tissue Engineering Part A
[Mary Ann Liebert, Inc.]
日期:2009-07-30
卷期号:16 (1): 101-114
被引量:107
标识
DOI:10.1089/ten.tea.2009.0106
摘要
Inadequate vascularization of in vitro–engineered tissue constructs after implantation is a major problem in most tissue-engineering applications. In this study we evaluated whether adipose tissue–derived stromal cells (ASCs), similar to bone marrow–derived stromal cells (BMSCs), can support the organization of endothelial cells into prevascular-like structures using an in vitro model. In addition, we investigated the mechanisms leading to the support of endothelial organization by these cells. We cultured human umbilical vein endothelial cells (HUVECs), ASCs, and BMSCs either alone or in combination in fibrin-embedded spheroids for 14 days. We found that BMSCs and ASCs formed cellular networks that expressed α smooth muscle actin and, in the case of ASCs, also CD34. Further, BMSCs and ASCs secreted hepatocyte growth factor and tissue inhibitor of metalloproteinase 1 and 2. In addition, ASC-conditioned medium induced HUVEC outgrowth, whereas BMSC-conditioned medium and hepatocyte growth factor–supplemented medium did not. Finally, both BMSCs and ASCs supported HUVEC organization into prevascular-like structures when cocultured. Our results suggest that both BMSCs and ASCs can support the formation of prevascular-like structures in vitro. Further, our findings indicate that cell–cell contacts and reciprocal signaling play an important role in the formation of these prevascular structures.
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