Human autologous serum obtained using a completely closed bag system as a substitute for foetal calf serum in human mesenchymal stem cell cultures

被引:75
作者
Mizuno, N
Shiba, H
Ozeki, Y
Mouri, Y
Niitani, M
Inui, T
Hayashi, H
Suzuki, K
Tanaka, S
Kawaguchi, H
Kurihara, H
机构
[1] Hiroshima Univ, Grad Sch Biomed Sci, Div Frontier Med Sci, Dept Periodontal Med,Minami Ku, Hiroshima 7348553, Japan
[2] JMS Co Ltd, Naka Ku, Hiroshima 7308652, Japan
基金
日本学术振兴会;
关键词
human autologous serum; human mesenchymal stem cell; cell therapy; cell proliferation; multipotency;
D O I
10.1016/j.cellbi.2006.01.010
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The major problem in cell therapy is the possibility of viral or bacterial infection and immune reactions. Therefore, it is expected of culture cells which are intended to be re-implanted with autologous serum rather than conventional bovine serum. Cell therapy with human mesenchymal stem cells (hMSC), differentiating to various cells, is thought to be curative. To culture hMSC with human autologous serum (HAS) and reimplant them for cell therapy, we developed a completely closed bag system separating serum, comparing proliferation and multipotency of hMSC cultured in HAS with those in foetal calf serum (FCS). HAS was simply, safely and efficiently obtained with the developed closed bag system. Cell proliferation of hMSC cultured in HAS was greater than that in FCS. hMSC, exposed to the defined induction medium containing HAS as well as FCS, differentiated into osteoblasts and adipocytes. These findings suggest that HAS obtained with the developed closed bag system is advantageous in a point of decrease in risk of virus or bacterial infection and foreign protein contamination and enhancement of proliferation of hMSC. (c) 2006 International Federation for Cell Biology. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:521 / 524
页数:4
相关论文
共 9 条
[1]  
Jaiswal N, 1997, J CELL BIOCHEM, V64, P295, DOI 10.1002/(SICI)1097-4644(199702)64:2<295::AID-JCB12>3.0.CO
[2]  
2-I
[3]   Cultured autologous human cells for hard tissue regeneration: Preparation and characterization of mesenchymal stem cells from bone marrow [J].
Kotobuki, N ;
Hirose, M ;
Takakura, Y ;
Ohgushi, H .
ARTIFICIAL ORGANS, 2004, 28 (01) :33-39
[4]   Multipotency of a bone marrow stromal cell line, TBR31-2, established from ts-SV40 T antigen gene transgenic mice [J].
Negishi, Y ;
Kudo, A ;
Obinata, A ;
Kawashima, K ;
Hirano, H ;
Yanai, N ;
Obinata, M ;
Endo, H .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 268 (02) :450-455
[5]  
NIJWEIDE PJ, 1990, BONE, V1, P303
[6]  
Noel Daniele, 2002, Curr Opin Investig Drugs, V3, P1000
[7]   Multilineage potential of adult human mesenchymal stem cells [J].
Pittenger, MF ;
Mackay, AM ;
Beck, SC ;
Jaiswal, RK ;
Douglas, R ;
Mosca, JD ;
Moorman, MA ;
Simonetti, DW ;
Craig, S ;
Marshak, DR .
SCIENCE, 1999, 284 (5411) :143-147
[8]   Autologous serum for isolation and expansion of human mesenchymal stem cells for clinical use [J].
Stute, N ;
Holtz, K ;
Bubenheim, M ;
Lange, C ;
Blake, F ;
Zander, AR .
EXPERIMENTAL HEMATOLOGY, 2004, 32 (12) :1212-1225
[9]   Retention of multilineage differentiation potential of mesenchymal cells during proliferation in response to FGF [J].
Tsutsumi, S ;
Shimazu, A ;
Miyazaki, K ;
Pan, H ;
Koike, C ;
Yoshida, E ;
Takagishi, K ;
Kato, Y .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 288 (02) :413-419