共 31 条
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.
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页码:869 / 875
页数:7
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