Ex Vivo Expansion of Human Mesenchymal Stem Cells in Defined Serum-Free Media

被引:113
作者
Jung, Sunghoon [1 ]
Panchalingam, Krishna M. [1 ]
Rosenberg, Lawrence [2 ]
Behie, Leo A. [1 ]
机构
[1] Univ Calgary, Pharmaceut Prod Res Facil, Schulich Sch Engn, Calgary, AB T2N 1N4, Canada
[2] McGill Univ, Dept Surg, Montreal, PQ H3G 1A4, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
HUMAN-BONE-MARROW; HUMAN PLATELET LYSATE; FETAL BOVINE SERUM; CLINICAL GRADE PRODUCTION; UMBILICAL-CORD BLOOD; HUMAN AB SERUM; STROMAL CELLS; ADIPOSE-TISSUE; CULTURE-CONDITIONS; AUTOLOGOUS SERUM;
D O I
10.1155/2012/123030
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Human mesenchymal stem cells (hMSCs) are presently being evaluated for their therapeutic potential in clinical studies to treat various diseases, disorders, and injuries. To date, early-phase studies have indicated that the use of both autologous and allogeneic hMSCs appear to be safe; however, efficacy has not been demonstrated in recent late-stage clinical trials. Optimized cell bioprocessing protocols may enhance the efficacy as well as safety of hMSC therapeutics. Classical media used for generating hMSCs are typically supplemented with ill-defined supplements such as fetal bovine serum (FBS) or human-sourced alternatives. Ideally, culture media are desired to have well-defined serum-free formulations that support the efficient production of hMSCs while maintaining their therapeutic and differentiation capacity. Towards this objective, we review here current cell culture media for hMSCs and discuss medium development strategies.
引用
收藏
页数:21
相关论文
共 117 条
[1]   Mesenchymal stem cells expanded in human platelet lysate display a decreased inhibitory capacity on T- and NK-cell proliferation and function [J].
Abdelrazik, Heba ;
Spaggiari, Grazia M. ;
Chiossone, Laura ;
Moretta, Lorenzo .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2011, 41 (11) :3281-3290
[2]   Feasibility and efficacy of bone tissue engineering using human bone marrow stromal cells cultivated in serum-free conditions [J].
Agata, Hideki ;
Watanabe, Nobukazu ;
Ishii, Yumiko ;
Kubo, Noriyuki ;
Ohshima, Satoshi ;
Yamazaki, Mika ;
Tojo, Arinobu ;
Kagami, Hideaki .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2009, 382 (02) :353-358
[3]   Human mesenchymal stem cells modulate allogeneic immune cell responses [J].
Aggarwal, S ;
Pittenger, MF .
BLOOD, 2005, 105 (04) :1815-1822
[4]   Mesenchymal stem cell therapy: Two steps forward, one step back [J].
Ankrum, James ;
Karp, Jeffrey M. .
TRENDS IN MOLECULAR MEDICINE, 2010, 16 (05) :203-209
[5]   Suitability of human mesenchymal stem cells for gene therapy depends on the expansion medium [J].
Apel, Anja ;
Groth, Ariane ;
Schlesinger, Sabine ;
Bruns, Helge ;
Schemmer, Peter ;
Buechler, Markus W. ;
Herr, Ingrid .
EXPERIMENTAL CELL RESEARCH, 2009, 315 (03) :498-507
[6]   Comparison of Human Placenta- and Bone Marrow-Derived Multipotent Mesenchymal Stem Cells [J].
Barlow, Sarah ;
Brooke, Gary ;
Chatterjee, Konica ;
Price, Gareth ;
Pelekanos, Rebecca ;
Rossetti, Tony ;
Doody, Marylou ;
Venter, Deon ;
Pain, Scott ;
Gilshenan, Kristen ;
Atkinson, Kerry .
STEM CELLS AND DEVELOPMENT, 2008, 17 (06) :1095-1107
[7]   METHODS FOR GROWTH OF CULTURED-CELLS IN SERUM-FREE MEDIUM [J].
BARNES, D ;
SATO, G .
ANALYTICAL BIOCHEMISTRY, 1980, 102 (02) :255-270
[8]   Two steps to functional mesenchymal stromal cells for clinical application [J].
Bartmann, Christina ;
Rohde, Eva ;
Schallmoser, Katharina ;
Puerstner, Peter ;
Lanzer, Gerhard ;
Linkesch, Werner ;
Strunk, Dirk .
TRANSFUSION, 2007, 47 (08) :1426-1435
[9]   Aggregation of human mesenchymal stromal cells (MSCs) into 3D spheroids enhances their antiinflammatory properties [J].
Bartosh, Thomas J. ;
Ylostalo, Joni H. ;
Mohammadipoor, Arezoo ;
Bazhanov, Nikolay ;
Coble, Katie ;
Claypool, Kent ;
Lee, Ryang Hwa ;
Choi, Hosoon ;
Prockop, Darwin J. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (31) :13724-13729
[10]   Human bone marrow-derived mesenchymal stem cells do not undergo transformation after long-term In vitro culture and do not exhibit telomere maintenance mechanisms [J].
Bernardo, Maria Ester ;
Zaffaroni, Nadia ;
Novara, Francesca ;
Cometa, Angela Maria ;
Avanzini, Maria Antonietta ;
Moretta, Antonia ;
Montagna, Daniela ;
Maccario, Rita ;
Villa, Raffaella ;
Daidone, Maria Grazia ;
Zuffardi, Orsetta ;
Locatelli, Franco .
CANCER RESEARCH, 2007, 67 (19) :9142-9149