Barroso Gerardo, Valdespin Carlos, Vega Eva, Kershenovich Ruben, Avila Rosaura, Avendaño Conrado, Oehninger Sergio
Reproductive Medicine and Infertility Division, National Institute of Perinatology, Mexico City, Mexico.
Reproductive Medicine and Infertility Division, National Institute of Perinatology, Mexico City, Mexico.
Fertil Steril. 2009 Sep;92(3):835-848. doi: 10.1016/j.fertnstert.2009.06.030. Epub 2009 Jul 24.
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 may be 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.
本综述的目的是研究各种被怀疑积极参与人类早期发育的精子成分的作用。受精精子对卵母细胞的贡献至少包括DNA/染色质的传递、一种假定的卵母细胞激活因子(OAF)和一个中心粒。最近的数据表明,精子还可能为受精卵提供一套独特的父本mRNA;一些转录本可能对胚胎的早期和晚期发育至关重要,传递不足或转录异常可能导致发育异常和停滞。辅助生殖的临床证据表明,受精过程、配子融合或早期卵裂未能完成可能是早期父本效应的结果。据推测,假定的OAF异常释放和/或中心体及细胞骨架装置功能障碍可能介导这些效应。另一方面,后期父本效应导致胚胎着床失败、妊娠丢失和/或由“遗留”的亚致死效应引起的发育异常,可能与精子核/染色质缺陷有关,包括非整倍体的存在、遗传异常、DNA损伤以及可能的其他原因。这些发现凸显了持续监测临床结果的必要性。