Platelet Lysate as a Serum Substitute for 2D Static and 3D Perfusion Culture of Stromal Vascular Fraction Cells from Human Adipose Tissue

被引:39
作者
Mueller, Andreas Marc [1 ]
Davenport, Michael [1 ]
Verrier, Sophie [2 ]
Droeser, Raoul [1 ]
Alini, Mauro [2 ]
Bocelli-Tyndall, Chiara [1 ,3 ]
Schaefer, Dirk J. [4 ]
Martin, Ivan [1 ]
Scherberich, Arnaud [1 ]
机构
[1] Univ Basel Hosp, Inst Surg Res & Hosp Management, Dept Biomed, Tissue Engn Grp,Lab 405, CH-4031 Basel, Switzerland
[2] AO Res Inst, Davos, Switzerland
[3] Felix Platter Hosp, Univ Dept Rheumatol, Basel, Switzerland
[4] Univ Basel Hosp, Dept Surg, Clin Plast Reconstruct & Aesthet Surg, CH-4031 Basel, Switzerland
关键词
MESENCHYMAL STEM-CELLS; FETAL CALF SERUM; ENDOTHELIAL-CELLS; AUTOLOGOUS SERUM; ANIMAL SERUM; RICH PLASMA; IN-VITRO; EXPANSION; DIFFERENTIATION; CONSTRUCTS;
D O I
10.1089/ten.tea.2008.0498
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Fetal bovine serum (FBS) and fibroblast growth factor (FGF)-2 are key supplements for the culture of stromal vascular fraction (SVF) cells from adipose tissue, both for typical monolayer (2D) expansion and for streamlined generation of osteogenic-vasculogenic grafts in 3D perfusion culture. The present study investigates whether factors present in human platelet lysate (PL) could substitute for FBS and FGF-2 in 2D and 3D culture models of SVF cells from human lipoaspirates. SVF cells were grown in medium supplemented with 10% FBS+FGF-2 or with 5% PL. In 2D cultures, PL initially supported SVF cell proliferation, but resulted in growth arrest shortly after the first passage. Freshly isolated SVF cells cultured with both media under perfusion for 5 days within 3D ceramic scaffolds induced bone formation after subcutaneous implantation in nude mice. However, blood vessels of donor origin were generated only using FBS+FGF-2-cultured cells. This was unexpected, because the proportion of CD34(+)/CD31(+) endothelial lineage cells was significantly higher with PL than that of FBS+FGF-2 (33% vs. 3%, respectively). These results support the use of PL as a substitute of FBS+FGF-2 for short-term culture of human SVF cells, and indicate that more specific serum-free formulations are required to maintain a functionally vasculogenic fraction of SVF cells expanded under 3D perfusion.
引用
收藏
页码:869 / 875
页数:7
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