Oocyte cryopreservation: a biological perspective

被引:37
作者
Coticchio, G
Bonu, MA
Borini, A
Flamigni, C
机构
[1] Univ Bologna, Tecnobios Procreaz, I-40125 Bologna, Italy
[2] Univ Bologna, Inst Obstet & Gynaecol, I-40125 Bologna, Italy
来源
EUROPEAN JOURNAL OF OBSTETRICS GYNECOLOGY AND REPRODUCTIVE BIOLOGY | 2004年 / 115卷
关键词
oocytes; cryopreservation; cytoskeleton; membrane permeability; fertilisation;
D O I
10.1016/j.ejogrb.2004.01.006
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Oocyte cryopreservation would amount to a major breakthrough in reproductive medicine. Diverse strategies have been tested to minimise cooling-induced cell injury. Nevertheless, oocytes from various species have shown a particular sensitivity to freezing, due to their unique biological characteristics. Storage of human mature oocytes with slow freezing has resulted in low survival rates, although recent studies based on modified methods have reported higher success. Survival after thawing is not necessarily a guarantee of unaltered viability. Developmental failure at pre- or postimplantation stages may originate from critical perturbations of various cell components, such as the chromosome segregation apparatus, the intracellular calcium signalling system, and the cytoskeleton. Germinal vesicle (GV)-stage oocytes have been suggested to be more amenable to freezing. But their use would require efficient in vitro maturation systems, which are not presently available. Oocyte cryopreservation remains a realistic objective, provided that more systematic approaches are applied, such as thorough analysis of the plasmalemma permeability to water and the diverse cryoprotectants. (C) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:S2 / S7
页数:6
相关论文
共 45 条
[1]   EVALUATION OF THE SPINDLE APPARATUS OF IN-VITRO MATURED HUMAN OOCYTES FOLLOWING CRYOPRESERVATION [J].
BAKA, SG ;
TOTH, TL ;
VEECK, LL ;
JONES, HW ;
MUASHER, SJ ;
LANZENDORF, SE .
HUMAN REPRODUCTION, 1995, 10 (07) :1816-1820
[2]  
Borini A, 1998, HUM REPROD, V13, P124
[3]   CYTOGENETICAL ANALYSIS AND DEVELOPMENTAL POTENTIAL OF VITRIFIED MOUSE OOCYTES [J].
BOSMIKICH, A ;
WOOD, MJ ;
CANDY, CJ ;
WHITTINGHAM, DG .
BIOLOGY OF REPRODUCTION, 1995, 53 (04) :780-785
[4]   ANALYSIS OF THE CHROMOSOME COMPLEMENT OF FROZEN-THAWED MOUSE OOCYTES AFTER PARTHENOGENETIC ACTIVATION [J].
BOSMIKICH, A ;
WHITTINGHAM, DG .
MOLECULAR REPRODUCTION AND DEVELOPMENT, 1995, 42 (02) :254-260
[5]   CRYOPRESERVATION OF IMMATURE MOUSE OOCYTES [J].
CANDY, CJ ;
WOOD, MJ ;
WHITTINGHAM, DG ;
MERRIMAN, JA ;
CHOUDHURY, N .
HUMAN REPRODUCTION, 1994, 9 (09) :1738-1742
[6]  
CARROLL J, 1990, J REPROD FERTIL, V90, P547, DOI 10.1530/jrf.0.0900547
[7]  
CARROLL J, 1989, J REPROD FERTIL, V85, P489, DOI 10.1530/jrf.0.0850489
[8]   NORMAL FERTILIZATION AND DEVELOPMENT OF FROZEN-THAWED MOUSE OOCYTES - PROTECTIVE ACTION OF CERTAIN MACROMOLECULES [J].
CARROLL, J ;
WOOD, MJ ;
WHITTINGHAM, DG .
BIOLOGY OF REPRODUCTION, 1993, 48 (03) :606-612
[9]   Use of fluorescence in situ hybridization to assess the chromosomal status of embryos obtained from cryopreserved oocytes [J].
Cobo, A ;
Rubio, C ;
Gerli, S ;
Ruiz, A ;
Pellicer, A ;
Remohí, J .
FERTILITY AND STERILITY, 2001, 75 (02) :354-360
[10]  
Coticchio G, 2001, Hum Fertil (Camb), V4, P152, DOI 10.1080/1464727012000199222