Autologous Platelet-Rich Plasma: A Biological Supplement to Enhance Adipose-Derived Mesenchymal Stem Cell Expansion

被引:0
|
作者
Atashi, Fatemeh [1 ]
Jaconi, Marisa E. E. [2 ]
Pittet-Cuenod, Brigitte [1 ]
Modarressi, Ali [1 ]
机构
[1] Univ Geneva, Fac Med, Univ Hosp Geneva HUG, Dept Plast Reconstruct & Aesthet Surg, Geneva, Switzerland
[2] Univ Geneva, Fac Med, Dept Pathol & Immunol, Geneva, Switzerland
基金
瑞士国家科学基金会;
关键词
FETAL BOVINE SERUM; CLINICAL-SCALE EXPANSION; GROWTH-FACTORS RELEASE; HUMAN BONE-MARROW; STROMAL CELLS; CALF SERUM; TISSUE; DIFFERENTIATION; PROLIFERATION; FAT;
D O I
10.1089/ten.tec.2014.0206
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Currently the use of non-autologous cell culture media (e.g., animal-derived or allogeneic serum) for clinical applications of mesenchymal stem cells (MSCs) is criticized by regulatory agencies. Autologous platelet-rich plasma (PRP) is proposed as a safer alternative medium supplement for adipose-derived mesenchymal stem cells (AT-MSC) culture. To study its efficiency on cell proliferation, AT-MSCs were cultured for 10 days in media supplemented with different concentrations of autologous non-activated PRP (nPRP) or thrombin-activated PRP (tPRP) (1-60%). AT-MSC proliferation, cell phenotype, multipotency capacity, and chromosome stability were assessed and compared to AT-MSCs expanded in a classical medium supplemented with 10% of fetal bovine serum (FBS). Culture media supplemented with nPRP showed dose-dependent higher AT-MSC proliferation than did FBS or tPRP. Twenty percent nPRP was the most effective concentration to promote cell proliferation. This condition increased 13.9 times greater AT-MSC number in comparison to culture with FBS, without changing the AT-MSC phenotype, differentiation capacity, and chromosome status. We concluded that 20% autologous nPRP is a safe, efficient, and cost-effective supplement for AT-MSC expansion. It should be considered as an alternative to FBS or other nonautologous blood derivatives. It could serve as a potent substitute for the validation of future clinical protocols as it respects good manufacturing practices and regulatory agencies' standards.
引用
收藏
页码:253 / 262
页数:10
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