Removal of inhibitory substances with recombinant fibronectin-CH-296 plates enhances the retroviral transduction efficiency of CD34+CD38- bone marrow cells

被引:14
作者
Chono, H [1 ]
Yoshioka, H [1 ]
Ueno, A [1 ]
Kato, I [1 ]
机构
[1] Takara Shuzo Co Ltd, Biotechnol Res Labs, Otsu, Shiga 5202193, Japan
关键词
bone marrow cells; CH-296; gene transfer; gibbon ape leukemia virus; retrovirus vector;
D O I
10.1093/oxfordjournals.jbchem.a002990
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In retroviral gene transduction, the efficiency of viral infection was reduced by the proteoglycans and some other materials secreted by the producer lines. In order to remove these inhibitors we have developed the rFN-CH-296-facilitated protocol. Because the rFN-CH-296 molecule has strong ability to bind a retroviral vector, rFN-CH-296 bound plates are utilized to wash out the unbound putative inhibitors present in a virus supernatant. The gene transduction efficiencies of human CD34(+)CD38(-) BMCs with a GALV-pseudotyped vector and the rFN-CH-296-facilitated protocol were compared with the protocol without a coating plate with CH-296, the mean gene transduction efficiencies being found to be 95.5 and 71.1%, respectively.
引用
收藏
页码:331 / 334
页数:4
相关论文
共 28 条
[1]  
Asada K, 1998, J BIOCHEM-TOKYO, V123, P1041
[2]   A simple and efficient method for the concentration and purification of recombinant retrovirus for increased hepatocyte transduction in vivo [J].
Bowles, NE ;
Eisensmith, RC ;
Mohuiddin, R ;
Pyron, M ;
Woo, SLC .
HUMAN GENE THERAPY, 1996, 7 (14) :1735-1742
[3]  
CHONO H, 2000, 6 ANN M 2000 JAP SOC
[4]  
CHONO H, 1999, 5 ANN M 1999 JAP SOC
[5]   Retroviral particles produced from a stable human-derived packaging cell line transduce target cells with very high efficiencies [J].
Davis, JL ;
Witt, RM ;
Gross, PR ;
Hokanson, CA ;
Jungles, S ;
Cohen, LK ;
Danos, O ;
Spratt, SK .
HUMAN GENE THERAPY, 1997, 8 (12) :1459-1467
[6]   A bioactive designer cytokine for human hematopoietic progenitor cell expansion [J].
Fischer, M ;
Goldschmitt, J ;
Peschel, C ;
Brakenhoff, JPG ;
Kallen, KJ ;
Wollmer, A ;
Grotzinger, J ;
RoseJohn, S .
NATURE BIOTECHNOLOGY, 1997, 15 (02) :142-145
[7]  
Forestell SP, 1995, GENE THER, V2, P723
[8]   Colocalization of retrovirus and target cells on specific fibronectin fragments increases genetic transduction of mammalian cells [J].
Hanenberg, H ;
Xiao, XL ;
Dilloo, D ;
Hashino, K ;
Kato, I ;
Williams, DA .
NATURE MEDICINE, 1996, 2 (08) :876-882
[9]   Optimization of fibronectin-assisted retroviral gene transfer into human CD34+ hematopoietic cells [J].
Hanenberg, H ;
Hashino, K ;
Konishi, H ;
Hock, RA ;
Kato, I ;
Williams, DA .
HUMAN GENE THERAPY, 1997, 8 (18) :2193-2206
[10]   Efficient retrovirus-mediated gene transfer to transplantable human bone marrow cells in the absence of fibronectin [J].
Hennemann, B ;
Oh, IH ;
Chuo, JY ;
Kalberer, CP ;
Schley, PD ;
Rose-John, S ;
Humphries, RK ;
Eaves, CJ .
BLOOD, 2000, 96 (07) :2432-2439