Genetic stability of bone marrow-derived human mesenchymal stromal cells in the Quantum System

被引:38
|
作者
Jones, Mark [1 ]
Varella-Garcia, Marileila [2 ]
Skokan, Margaret [2 ]
Bryce, Steven [3 ]
Schowinsky, Jeffrey [4 ]
Peters, Rebecca [1 ]
Vang, Boah [1 ]
Brecheisen, Michelle [1 ]
Startz, Thomas [1 ]
Frank, Nathan [1 ]
Nankervis, Brian [1 ]
机构
[1] Terumo BCT Inc, Lakewood, CO 80215 USA
[2] Univ Colorado Denver, Sch Med, Div Med Oncol, Aurora, CO USA
[3] Litron Labs, Rochester, NY USA
[4] Univ Colorado Hosp, Dept Pathol, Aurora, CO USA
关键词
cell proliferation; chromosome; mesenchymal stromal cell; micronucleus; spectral karyotyping; xenograft; VITRO MICRONUCLEUS ASSAY; IN-VITRO; STEM-CELLS; FLOW-CYTOMETRY; DAMAGE; TRANSPLANTS; INSTABILITY; POPULATION; RESTORES; CULTURES;
D O I
10.1016/j.jcyt.2013.05.024
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Background aims. The Quantum Cell Expansion System (Quantum; Terumo BCT, Inc, Lakewood, CO, USA) is a novel hollow fiber-based device that automates and closes the cell culture process, reducing labor intensive tasks such as manual cell culture feeding and harvesting. The manual cell selection and expansion processes for the production of clinical-scale quantities of bone marrow-derived human mesenchymal stromal cells (BM-hMSCs) have been successfully translated onto the Quantum platform previously. The formerly static, manual, in vitro process performed primarily on tissue culture polystyrene substrates may raise the question of whether BM-hM.SCs cultured on a hollow fiber platform yields comparable cell quality. Methods. A rigorous battery of assays was used to determine the genetic stability of BM-hMSCs selected and produced with the Quantum. In this study, genetic stability was determined by assessing spectral karyotype, micronucleus formation and tumorigenicity to resolve chromosomal aberrations in the stem cell population. Cell phenotype, adherent growth kinetics and tri-lineage differentiation were also evaluated. HMSC bone marrow aspirates, obtained from three approved donors, were expanded in parallel using T225 culture flasks and the Quantum. Results. BM-hMSCs harvested from the Quantum demonstrated immunophenotype, morphology and tri-lineage differentiation capacity characteristics consistent with the International Society of Cell Therapy standard for hMSCs. Cell populations showed no malignant neoplastic formation in athymic mice 60 days post-transplant, no clonal chromosomal aberrations were observed and no DNA damage was found as measured by micronucleus formation. Conclusions. Quantum-produced BM-hMSCs are of comparable quality and demonstrate analogous genetic stability to BM-hMSCs cultured on tissue culture polystyrene substrates.
引用
收藏
页码:1323 / 1339
页数:17
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