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
相关论文
共 50 条
  • [21] A LOCAL CELL-BASED DELIVERY SYSTEM FOR HUMAN GLIOMAS USING HUMAN BONE MARROW-DERIVED MESENCHYMAL STROMAL CELLS
    Menon, Lata G.
    Armant, Myriam
    Badr, Christian
    Bakhos, Tannous A.
    Yang, Hongwei
    Pratt, John
    Sorensen, A. Gregory
    Black, Peter Mclaren
    Carroll, Rona S.
    NEURO-ONCOLOGY, 2009, 11 (05) : 589 - 589
  • [22] Molecular signature of human bone marrow-derived mesenchymal stromal cell subsets
    Selim Kuçi
    Zyrafete Kuçi
    Richard Schäfer
    Gabriele Spohn
    Stefan Winter
    Matthias Schwab
    Emilia Salzmann-Manrique
    Thomas Klingebiel
    Peter Bader
    Scientific Reports, 9
  • [23] Bone marrow-derived mesenchymal stromal cells accelerate wound healing in the rat
    McFarlin, Kellie
    Gao, Xiaohua
    Liu, Yong Bo
    Dulchavsky, Deborah S.
    Kwon, David
    Arbab, Ali S.
    Bansal, Mona
    Li, Yi
    Chopp, Michael
    Dulchavsky, Scott A.
    Gautam, Subhash C.
    WOUND REPAIR AND REGENERATION, 2006, 14 (04) : 471 - 478
  • [24] Molecular signature of human bone marrow-derived mesenchymal stromal cell subsets
    Kuci, Selim
    Kuci, Zyrafete
    Schaefer, Richard
    Spohn, Gabriele
    Winter, Stefan
    Schwab, Matthias
    Salzmann-Manrique, Emilia
    Klingebiel, Thomas
    Bader, Peter
    SCIENTIFIC REPORTS, 2019, 9 (1)
  • [25] The therapeutic potential of bone marrow-derived mesenchymal stromal cells on hepatocellular carcinoma
    Bayo, Juan
    Marrodan, Mariano
    Aquino, Jorge B.
    Silva, Marcelo
    Garcia, Mariana G.
    Mazzolini, Guillermo
    LIVER INTERNATIONAL, 2014, 34 (03) : 330 - 342
  • [26] Ultrastructural study of cultured ovine bone marrow-derived mesenchymal stromal cells
    Desantis, Salvatore
    Accogli, Gianluca
    Zizza, Sara
    Mastrodonato, Maria
    Blasi, Antonella
    Francioso, Edda
    Rossi, Roberta
    Crovace, Antonio
    Resta, Leonardo
    ANNALS OF ANATOMY-ANATOMISCHER ANZEIGER, 2015, 201 : 43 - 49
  • [27] Route of delivery influences biodistribution of human bone marrow-derived mesenchymal stromal cells following experimental bone marrow transplantation
    Wang, F. J.
    Eid, S.
    Dennis, J. E.
    Cooke, K. R.
    Auletta, J. J.
    Lee, Z.
    JOURNAL OF STEM CELLS & REGENERATIVE MEDICINE, 2015, 11 (02): : P34 - P43
  • [28] Bone marrow stromal cells (bone marrow-derived multipotent mesenchymal stromal cells) for bone tissue engineering: Basic science to clinical translation
    Kagami, Hideaki
    Agata, Hideki
    Tojo, Arinobu
    INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2011, 43 (03): : 286 - 289
  • [29] A Comparison of Human Bone Marrow-Derived Mesenchymal Stem Cells and Human Umbilical Cord-Derived Mesenchymal Stromal Cells for Cartilage Tissue Engineering
    Wang, Limin
    Tran, Ivy
    Seshareddy, Kiran
    Weiss, Mark L.
    Detamore, Michael S.
    TISSUE ENGINEERING PART A, 2009, 15 (08) : 2259 - 2266
  • [30] Bone marrow-derived mesenchymal stem cells
    Kemp, KC
    Hows, J
    Donaldson, C
    LEUKEMIA & LYMPHOMA, 2005, 46 (11) : 1531 - 1544