Isolation, expansion and characterization of bone marrow-derived mesenchymal stromal cells in serum-free conditions

被引:41
作者
Gottipamula, Sanjay [1 ]
Ashwin, K. M. [1 ]
Muttigi, Manjunatha S. [1 ]
Kannan, Suresh [2 ]
Kolkundkar, Udaykumar [2 ]
Seetharam, Raviraja N. [1 ]
机构
[1] Stempeut Res Pvt Ltd, Shirdi Sai Baba Canc Hosp, Manipal, Karnataka, India
[2] Stempeut Res Pvt Ltd, Bangalore, Karnataka, India
关键词
Bone marrow; Differentiation; Isolation; kinetics; Mesenchymal stromal cells; Phenotypic; characterization; Serum-free media; Xeno-freemedia; EX-VIVO EXPANSION; FIBROBLAST-GROWTH-FACTOR; FETAL BOVINE SERUM; STEM-CELLS; INTERNATIONAL-SOCIETY; CULTURE-CONDITIONS; PLATELET LYSATE; PROLIFERATION; SUBSTITUTE; EFFICACY;
D O I
10.1007/s00441-013-1783-7
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Bone marrow-derived mesenchymal stromal cells (BM-MSCs) heralded a new beginning for regenerative medicine and generated tremendous interest as the most promising source for therapeutic application. Most cell therapies require stringent regulatory compliance and prefer the use of serum-free media (SFM) or xeno-free media (XFM) for the MSC production process, starting from the isolation onwards. Here, we report on serum-free isolation and expansion of MSCs and compare them with cells grown in conventional fetal bovine serum (FBS)-containing media as a control. The isolation, proliferation and morphology analysis demonstrated significant differences between MSCs cultured in various SFM/XFM in addition to their difference with FBS controls. BD Mosaic (TM) Mesenchymal Stem Cell Serum-Free media (BD-SFM) and Mesencult-XF (MSX) supported the isolation, sequential passaging, tri-lineage differentiation potential and acceptable surface marker expression profile of BM-MSCs. Further, MSCs cultured in SFM showed higher immune suppression and hypo-immunogenicity properties, making them an ideal candidate for allogeneic cell therapy. Although cells cultured in control media have a significantly higher proliferation rate, BM-MSCs cultured in BD-SFM or MSX media are the preferred choice to meet regulatory requirements as they do not contain bovine serum. While BM-MSCs cultured in BD-SFM and MSX media adhered to all MSC characteristics, in the case of few parameters, the performance of cells cultured in BD-SFM was superior to that of MSX media. Pre-clinical safety and efficiency studies are required before qualifying SFM or XFM media-derived MSCs for therapeutic applications.
引用
收藏
页码:123 / 135
页数:13
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