Chromosome instability in Spodoptera frugiperda Sf-9 cell line

被引:16
作者
Jarman-Smith, RF
Armstrong, SJ
Mannix, CJ
Al-Rubeai, M [1 ]
机构
[1] Univ Birmingham, Dept Chem Engn, Anim Cell Technol Grp, Birmingham B15 2TT, W Midlands, England
[2] Univ Birmingham, Sch Biosci, Birmingham B15 2TT, W Midlands, England
[3] GlaxoSmithKline, Microbial & Cell Culture Sci, Harlow CM19 5AW, Essex, England
关键词
D O I
10.1021/bp020028+
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Homogeneous cell lines are essential in industry and research if reliable and reproducible data are to be obtained. The Spodoptera frugaperda (Sf-9) cell line routinely used for the production of recombinant proteins was found to be heterogeneous, containing a mixture of diploid and tetraploid cells. Using dilution-cloning techniques, diploid and tetraploid subpopulations were isolated from a Sf-9 parental cell line, and their cytogenetic state was monitored using Vinblastine to arrest cells in mitosis. Flow cytometry was used to obtain a snapshot of the predominant subpopulations present to verify the karyological results. The rate at which clonal populations digress into the heterogeneous state was found to be more rapid for the diploid subpopulation, with the emergence of tetraploid cells after only 11 passages, than for the tetraploid subpopulation, where diploid clones appeared after 18 passages. The chromosomes in both diploid and tetraploid subpopulations as well as the parental cell line were found to spontaneously fragment during growth and expansion processes, giving rise to variable chromosome numbers. DNA analysis of cell lines obtained from laboratories worldwide have shown that the Sf-9 cell line used for the production of many recombinant proteins is cytologically unstable, leading to varying degrees of polyploidal state depending on its culture history and supplier.
引用
收藏
页码:623 / 628
页数:6
相关论文
共 19 条
[1]   CELL-CYCLE AND CELL-SIZE DEPENDENCE OF SUSCEPTIBILITY TO HYDRODYNAMIC-FORCES [J].
ALRUBEAI, M ;
SINGH, RP ;
EMERY, AN ;
ZHANG, Z .
BIOTECHNOLOGY AND BIOENGINEERING, 1995, 46 (01) :88-92
[2]  
ALRUBEAI M, 1992, ANIMAL CELL TECHNOLOGY : DEVELOPMENTS, PROCESSES AND PRODUCTS, P301
[3]  
*AM TYP CULT COLL, 1988, CAT CELL LIN HYBR, P166
[4]  
BERNHARD H, 1980, INVERTEBRATE SYSTEMS, P15
[5]  
Center for Biologics Evaluation and Research, 1993, POINTS CONS CHAR CEL
[6]  
DISNEY JE, 1985, IN VITRO CELL DEV B, V21, P563
[7]  
Doran P. M., 1995, BIOPROCESS ENG PRINC
[8]   Cell cycle progression in serum-free cultures of Sf9 insect cells:: Modulation by conditioned medium factors and implications for proliferation and productivity [J].
Doverskog, M ;
Bertram, E ;
Ljunggren, J ;
Öhman, L ;
Sennerstam, R ;
Häggström, L .
BIOTECHNOLOGY PROGRESS, 2000, 16 (05) :837-846
[9]   CELL-CYCLE KINETICS OF INSECT CELL-CULTURES COMPARED TO MAMMALIAN-CELL CULTURES [J].
FERTIG, G ;
KLOPPINGER, M ;
MILTENBURGER, HG .
EXPERIMENTAL CELL RESEARCH, 1990, 189 (02) :208-212
[10]  
Francki R. I. B., 1991, 5 REPORT INT COMMITT