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Serum‐free human MSC medium supports consistency in human but not in equine adipose‐derived multipotent mesenchymal stromal cell culture
Author(s) -
Schubert Susanna,
Brehm Walter,
Hillmann Aline,
Burk Janina
Publication year - 2018
Publication title -
cytometry part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.316
H-Index - 90
eISSN - 1552-4930
pISSN - 1552-4922
DOI - 10.1002/cyto.a.23240
Subject(s) - mesenchymal stem cell , adipose tissue , stromal cell , cell culture , microbiology and biotechnology , cell , biology , chemistry , cancer research , endocrinology , biochemistry , genetics
For clinical applications of multipotent mesenchymal stromal cells (MSCs), serum‐free culture is preferable to standardize cell products and prevent contamination with pathogens. In contrast to human MSCs, knowledge on serum‐free culture of large animal MSCs is limited, despite its relevance for preclinical studies and development of veterinary cellular therapeutics. This study aimed to evaluate the suitability of a commercially available serum‐free human MSC medium for culturing equine adipose‐derived MSCs in comparison with human adipose MSCs. Enzyme‐free isolation by explant technique and expansion of equine and human cells in the serum‐free medium were feasible. However, serum‐free culture altered the morphology and complicated handling of equine MSCs, with cell aggregation and spontaneous detachment of multilayers, compared to culture in standard medium supplemented with fetal bovine serum. Furthermore, proliferation and the surface immunophenotype of equine cells were more variable compared to the controls and appeared to depend on the lot of the serum‐free medium. Particularly the expression of CD90 was different between experimental groups ( P < 0.05), with lower percentages of CD90 + cells found in equine MSC samples cultured in serum‐free medium (5.21–83.40%) compared to standard medium (86.20–99.50%). Additionally, small subpopulations expressing MSC exclusion markers such as CD14 (0.28–11.60%), CD34 (0.00–9.87%), CD45 (0.35–10.50%), or MHCII (0.00–3.67%) were found in equine samples after serum‐free culture. In contrast, human samples displayed a more consistent morphology and a consistent CD29 + (98.60–99.90%), CD73 + (94.60–98.40%), CD90 + (99.60–99.90%), and CD105 + (97.40–99.80%) immunophenotype after culture in serum‐free medium. The obtained data demonstrate that the serum‐free medium was suitable for human MSC culture but did not lead to entirely satisfactory results in equine MSCs. This underlines that requirements regarding serum‐free culture conditions are species‐specific, indicating a need for serum‐free media to be optimized for MSCs from relevant animal species. © 2017 International Society for Advancement of Cytometry