Developmental sperm contributions: fertilization and beyond

被引:115
作者
Barroso, Gerardo [1 ]
Valdespin, Carlos [1 ]
Vega, Eva [1 ]
Kershenovich, Ruben [1 ]
Avila, Rosaura [1 ]
Avendano, Conrado [2 ]
Oehninger, Sergio [2 ]
机构
[1] Natl Inst Perinatol, Reprod Med & Infertil Div, Mexico City 11000, DF, Mexico
[2] Eastern Virginia Med Sch, Jones Inst Reprod Med, Dept Obstet & Gynecol, Norfolk, VA USA
关键词
Embryogenesis; fertilization; paternal contribution; spermatozoa; IN-VITRO FERTILIZATION; DEOXYRIBONUCLEIC-ACID FRAGMENTATION; PLASMA-MEMBRANE TRANSLOCATION; INDUCED CALCIUM OSCILLATIONS; CHROMATIN-STRUCTURE ASSAY; MALE FACTOR INFERTILITY; NUCLEAR-DNA DAMAGE; ZONA-PELLUCIDA; MAMMALIAN SPERM; MITOCHONDRIAL-DNA;
D O I
10.1016/j.fertnstert.2009.06.030
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
The objective of this review was to examine the role of the various spermatozoal components suspected of actively participating in early human development. The contributions of the fertilizing spermatozoon to the oocyte include, as a minimum, the delivery of the DNA/chromatin, a putative oocyte-activating factor (OAF), and a centriole. Recent data indicate that spermatozoa may also provide the zygote with a unique suite of paternal mRNAs; some transcripts might be crucial for early and late embryonic development and deficient delivery, or aberrant transcription might contribute to abnormal development and arrest, Clinical evidence from assisted reproduction suggests that failure to complete the fertilization process, syngamy, or early cleavage might be the result of an early paternal effect. It is speculated that an abnormal release of a putative OAF and/or dysfunctions of the centrosome and cytoskeletal apparatus may mediate these effects. On the other hand, a later paternal effect resulting in embryonic failure to achieve implantation, pregnancy loss, and/or developmental abnormalities resulting from "carried over" sublethal effects maybe associated with sperm nuclear/chromatin defects, including the presence of aneuploidy, genetic anomalies, DNA damage, and possibly other causes. These findings highlight the need for continuous monitoring of clinical results. (Fertil Steril (R) 2009;92:835-48. (C)2009 by American Society for Reproductive Medicine.)
引用
收藏
页码:835 / 848
页数:14
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