Cytoskeletal organization defects and abortive activation in human oocytes after IVF and ICSI failure

被引:106
作者
Rawe, VY [1 ]
Olmedo, SB
Nodar, FN
Doncel, GD
Acosta, AA
Vitullo, AD
机构
[1] IOSS, Ctr Estudios Ginecol & Reprod, RA-1055 Buenos Aires, DF, Argentina
[2] Eastern Virginia Med Sch, Jones Inst Reprod Med, Dept Obstet & Gynecol, Norfolk, VA 23507 USA
关键词
abortive activation; cytoskeletal organization; fertilization failure; microtubules;
D O I
10.1093/molehr/6.6.510
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
In this study, we analysed the distribution of beta tubulins to detect spindle and cytoplasmic microtubules, a acetylated tubulins for sperm microtubules and chromatin configuration in oocytes showing fertilization failure after conventional IVF or intracytoplasmic sperm injection (ICSI). A total of 450 human oocytes that failed to fertilize were studied 20-40 h after IVF or ICSI. In all, 287 oocytes were stained for immunofluorescence and chromosomal spreads were performed by Tarkowski's air-drying method in 163 IVF or ICSI oocytes that did not develop pronuclei after the extrusion of a second polar body. Immunofluorescence analysis showed that the main reason of fertilization failure after IVF was no sperm penetration (55.5%). The remaining oocytes showed different abnormal patterns, e.g. oocyte activation failure (15.1%) and defects in pronuclei apposition (19.2%). On the other hand, fertilization failure after ICSI was mainly associated to incomplete oocyte activation (39.9%), and to a lesser extent with defects in pronuclei apposition (22.6%) and failure of sperm penetration (13.3%). A further 13.3% of the ICSI oocytes arrested their development at the metaphase of the first mitotic division. The chromosomal spreads allowed the analysis of abortive activations, in which no pronuclei formed but a second polar body was extruded. Immunofluorescence and cytogenetic analysis provided a useful tool to improve infertility diagnosis and prognosis in each particular case.
引用
收藏
页码:510 / 516
页数:7
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