Differential Gene Expression in Adipose Stem Cells Cultured in Allogeneic Human Serum Versus Fetal Bovine Serum

被引:0
作者
Lindroos, Bettina [1 ]
Aho, Kaisa-Leena [3 ]
Kuokkanen, Hannu [2 ]
Raty, Sari [4 ]
Huhtala, Heini [5 ]
Lemponen, Riina [5 ]
Yli-Harja, Olli [3 ]
Suuronen, Riitta [1 ,6 ,7 ]
Miettinen, Susanna [1 ]
机构
[1] Univ Tampere, Regea Inst Regenerat Med, Tampere 33520, Finland
[2] Tampere Univ Hosp, Dept Plast Surg, Tampere 33520, Finland
[3] Tampere Univ Technol, Dept Signal Proc, FIN-33101 Tampere, Finland
[4] Tampere Univ Hosp, Dept Gastroenterol & Alimentary Tract Surg, Tampere 33520, Finland
[5] Univ Tampere, Tampere Sch Publ Hlth, Tampere 33520, Finland
[6] Tampere Univ Hosp, Dept Eye Ear & Oral Dis, Tampere 33520, Finland
[7] Tampere Univ Technol, Dept Biomed Engn, FIN-33101 Tampere, Finland
基金
芬兰科学院;
关键词
MESENCHYMAL STROMAL CELLS; BONE MORPHOGENETIC PROTEIN-2; HUMAN PLATELET LYSATE; TGF-BETA; IN-VITRO; CALF SERUM; ADIPOCYTE DIFFERENTIATION; AUTOLOGOUS SERUM; TISSUE; GROWTH;
D O I
10.1089/ten.tea.2009.0621
中图分类号
Q813 [细胞工程];
学科分类号
摘要
In preclinical studies, human adipose stem cells (ASCs) have been shown to have therapeutic applicability, but standard expansion methods for clinical applications remain yet to be established. ASCs are typically expanded in the medium containing fetal bovine serum (FBS). However, sera and other animal-derived culture reagents stage safety issues in clinical therapy, including possible infections and severe immune reactions. By expanding ASCs in the medium containing human serum (HS), the problem can be eliminated. To define how allogeneic HS (alloHS) performs in ASC expansion compared to FBS, a comparative in vitro study in both serum supplements was performed. The choice of serum had a significant effect on ASCs. First, to reach cell proliferation levels comparable with 10% FBS, at least 15% alloHS was required. Second, while genes of the cell cycle pathway were overexpressed in alloHS, genes of the bone morphogenetic protein receptor-mediated signaling on the transforming growth factor beta signaling pathway regulating, for example, osteoblast differentiation, were overexpressed in FBS. The result was further supported by differentiation analysis, where early osteogenic differentiation was significantly enhanced in FBS. The data presented here underscore the importance of thorough investigation of ASCs for utilization in cell therapies. This study is a step forward in the understanding of these potential cells.
引用
收藏
页码:2281 / 2294
页数:14
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