Couplet alignment and improved electrofusion by dielectrophoresis for a zona-free high-throughput cloned embryo production system

被引:25
作者
Gaynor, P [1 ]
Wells, DN
Oback, B
机构
[1] Univ Waikato, Dept Phys & Elect Engn, Hamilton, New Zealand
[2] AgResearch, Ruakura Res Ctr, Reprod Technol, Hamilton, New Zealand
关键词
cloning; dielectrophoresis; electrofusion; zona-free; nuclear transfer;
D O I
10.1007/BF02345137
中图分类号
TP39 [计算机的应用];
学科分类号
081203 [计算机应用技术]; 0835 [软件工程];
摘要
Mammalian cloning by somatic nuclear transfer has great potential for developing medical applications such as biopharmaceuticals and generation of tissues for transplantation. For agricultural applications, it allows the rapid dissemination of genetic gain in livestock breeding. The maximisation of that potential requires improvements to overall cloning technology, especially with respect to increasing cloning efficiency and throughput rates in cloned embryo production. A zona-free embryo reconstruction system was developed to increase cloning throughput and ease of operation. Central to this system is a modified electrofusion procedure for nuclear transfer. Cytoplast-donor cell couplets were placed in a custom-designed 'parallel plate' electrode chamber. A 1 MHz sinusoidal AC dielectrophoresis alignment electric field of 6-10 kV m(-1) was applied for 5-10 s. The couplets were then fused using 2 x 10 mus rectangular DC-field pulses (150-200 kV m-1), followed by application of the AC field (6-10 kV m-1) for another 5-10 s. Fusion was performed in hypoosmolar buffer (210 mOsm). Automated alignment of up to 20 couplets at a time has been achieved, resulting in greatly improved fusion throughput rates (2.5-fold increase) and improved fusion yields (1.3-fold increase), compared with commonly followed zona-intact protocols.
引用
收藏
页码:150 / 154
页数:5
相关论文
共 16 条
[1]
IMPROVED DEVELOPMENT TO BLASTOCYST OF OVINE NUCLEAR TRANSFER EMBRYOS RECONSTRUCTED DURING THE PRESUMPTIVE S-PHASE OF ENUCLEATED ACTIVATED OOCYTES [J].
CAMPBELL, KHS ;
LOI, P ;
CAPPAI, P ;
WILMUT, I .
BIOLOGY OF REPRODUCTION, 1994, 50 (06) :1385-1393
[2]
Sheep cloned by nuclear transfer from a cultured cell line [J].
Campbell, KHS ;
McWhir, J ;
Ritchie, WA ;
Wilmut, I .
NATURE, 1996, 380 (6569) :64-66
[3]
Therapeutic cloning: concepts and practicalities [J].
Colman, A ;
Kind, A .
TRENDS IN BIOTECHNOLOGY, 2000, 18 (05) :192-196
[4]
Jones T.B., 2005, Electromechanics of particles
[5]
Cloned transchromosomic calves producing human immunoglobulin [J].
Kuroiwa, Y ;
Kasinathan, P ;
Choi, YJ ;
Naeem, R ;
Tomizuka, K ;
Sullivan, EJ ;
Knott, JG ;
Duteau, A ;
Goldsby, RA ;
Osborne, BA ;
Ishida, I ;
Robl, JM .
NATURE BIOTECHNOLOGY, 2002, 20 (09) :889-894
[6]
Lagutina I., 2003, Theriogenology, V59, P269
[7]
Generation of histocompatible tissues using nuclear transplantation [J].
Lanza, RP ;
Chung, HY ;
Yoo, JJ ;
Wettstein, PJ ;
Blackwell, C ;
Borson, N ;
Hofmeister, E ;
Schuch, G ;
Soker, S ;
Moraes, CT ;
West, MD ;
Atala, A .
NATURE BIOTECHNOLOGY, 2002, 20 (07) :689-696
[8]
ELECTROFUSION [J].
NEIL, GA ;
ZIMMERMANN, U .
METHODS IN ENZYMOLOGY, 1993, 220 :174-196
[9]
Neumann E., 1989, ELECTROPORATION ELEC
[10]
Cloning cattle [J].
Oback, B ;
Wells, DN .
CLONING AND STEM CELLS, 2003, 5 (04) :243-256