Amiel M L, Duquenne C, Benveniste J, Testart J
INSERM U187, Hôpital Antoine Béclère, Clamart, France.
Hum Reprod. 1989 Apr;4(3):327-30. doi: 10.1093/oxfordjournals.humrep.a136898.
A factor activating human platelets and liberated by the embryo was sought in the culture media of human embryos using two bioassays. The first bioassay demonstrated the existence of a thrombocytopaenic factor after the i.p. injection of culture media into splenectomized mice. This factor was found more frequently in media which contained an embryo compared to those which contained a non-fertilized oocyte. PAF-acether (1-O-alkyl-2-acetyl-sn-glycero-3-phosphocholine) was searched for with a specific bioassay, using washed rabbit platelets. This remained negative for all the media studied, including those which had contained an embryo giving rise to a pregnancy. In these experiments it was not possible to relate embryo-derived platelet activating factor (EDPAF) to PAF-acether. Neither were we able to use the detection of EDPAF to test embryonic viability, or attempt to identify those embryos which were susceptible to lead to a pregnancy after intrauterine transfer from among all the embryos transferred.
利用两种生物测定法,在人类胚胎的培养基中寻找一种可激活人类血小板并由胚胎释放的因子。第一种生物测定法显示,将培养基腹腔注射到脾切除的小鼠体内后,存在一种血小板减少因子。与含有未受精卵母细胞的培养基相比,在含有胚胎的培养基中更频繁地发现这种因子。使用洗涤过的兔血小板,通过特定的生物测定法寻找血小板活化因子(PAF-乙醚,1-O-烷基-2-乙酰基-sn-甘油-3-磷酸胆碱)。对于所有研究的培养基,包括那些孕育出妊娠的含有胚胎的培养基,该测定结果均为阴性。在这些实验中,无法将胚胎衍生的血小板活化因子(EDPAF)与PAF-乙醚联系起来。我们也无法利用EDPAF的检测来测试胚胎活力,或尝试从所有移植的胚胎中识别出那些在子宫内移植后易导致妊娠的胚胎。