Comparative Analysis of Media and Supplements on Initiation and Expansion of Adipose-Derived Stem Cells
Open Access
- 2 February 2016
- journal article
- research article
- Published by Oxford University Press (OUP) in Stem Cells Translational Medicine
- Vol. 5 (3) , 314-324
Abstract
Adipose-derived stem cells (ASCs) are being tested in clinical trials related to cell-based regenerative therapies. Although most of the current expansion protocols for ASCs use fetal calf serum (FCS), xenogeneic-free medium supplements are greatly desired. This study aims to compare the effect of FCS, human platelet lysate (hPL), and a fully defined medium on the initiation and maintenance of ASC cultures. ASCs obtained from five donors were cultured in five different media: StemPro, Dulbecco's modified Eagle's medium (DMEM) supplemented with 10% hPL, or α-minimum essential medium (A-MEM) supplemented with 5% hPL, 10% hPL, or 10% FCS. The effect of media on proliferation, colony-forming units (CFUs), attachment, and morphology was assessed along with cell size, granularity, and immunophenotype. StemPro greatly compromised the initiation of ASC cultures, which could not survive more than a few passages. Cells cultured in A-MEM proliferated at a faster rate than in DMEM, and hPL significantly enhanced cell size, granularity, and proliferation compared with FCS. All media except StemPro supported CFUs equally well. Analysis of surface markers revealed higher levels of CD73 and CD105 in FCS-cultured ASCs, whereas increased levels of CD146 were found in hPL-cultured cells. Multiparametric flow cytometric analysis performed after seven passages revealed the existence of four distinct ASC subpopulations, all positive for CD73, CD90, and CD105, which mainly differed by their expression of CD146 and CD271. Analysis of the different subpopulations might represent an important biological measure when assessing different medium formulations for a particular clinical application. Significance: In most clinical trials using adipose-derived stem cells (ASCs), the cells have been expanded in culture media supplemented with fetal calf serum. However, there is much interest in replacing fetal calf serum with human platelet lysate or using completely serum- and xenogeneic-free media. This study found that culture in fetal calf serum versus human platelet lysate had a significant effect on the degree of expression of stem cell–associated surface markers. These results underscore the need to carefully investigate the effect of culture media on ASC behavior before committing to one medium type for clinical use.Keywords
Funding Information
- Lily Benthine Lunds Fond (5652)
- Obelske Family Foundation (20114-18036)
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