Porter A J, Singh S M, Jung J H
Department of Zoology, Children's Hospital of Western Ontario, London, Canada.
Mutagenesis. 1988 Sep;3(5):403-8. doi: 10.1093/mutage/3.5.403.
Reproductive failures may be caused by chromosomal anomalies, complex interactions of maternal/fetal genotype and environmental factors. Some of them have also been attributed to undefined maternal serum factor(s). We have developed an assay to evaluate maternal-serum associated embryotoxicity/mutagenicity using the preimplantation mouse embryo. It is based on in vitro culture of 8-cell mouse embryos for 48 h in the presence of 10% sera from females with reproductive dysfunction along with suitable controls. The human sera were obtained from three groups of females: (i) with normal reproductive histories (negative controls), (ii) undergoing cancer chemotherapy (positive controls), and (iii) with a history of failing to achieve or maintain pregnancy (test group). The preimplantation mouse embryos were cultured in the three types of human sera and female rat serum (as an internal control for each experiment) and evaluated for toxicity (embryo survival) and mutagenicity (as measured by SCE). Embryos cultured in serum from women with normal reproductive histories and female rats had survival rates of 70.8 +/- 4.3 and 78.9 +/- 0.9%, respectively. The SCE frequencies for these two sera types were similar: 15.7 +/- 0.2 SCEs/cell (rat) and 16.3 +/- 0.3 SCEs/cell (human). Mouse embryos cultured in medium supplemented with serum from females undergoing chemotherapy had significantly (P less than 0.01) reduced survival (33.7 +/- 5.2%) and significantly (P less than 0.01) increased SCEs/cell (26.5 +/- 0.6). The effect of sera from women with histories of reproductive failures on preimplantation mouse embryos was variable and individual specific. Approximately 40% of the test group female sera yielded survival and SCEs/cell comparable to the sera from patients undergoing chemotherapy.(ABSTRACT TRUNCATED AT 250 WORDS)
生殖失败可能由染色体异常、母体/胎儿基因型与环境因素的复杂相互作用引起。其中一些也归因于未明确的母体血清因子。我们开发了一种检测方法,使用植入前小鼠胚胎来评估母体血清相关的胚胎毒性/致突变性。该方法基于在含有来自生殖功能障碍雌性动物的10%血清以及合适对照的情况下,将8细胞小鼠胚胎进行体外培养48小时。人血清取自三组女性:(i)有正常生殖史的(阴性对照),(ii)正在接受癌症化疗的(阳性对照),以及(iii)有未能受孕或维持妊娠史的(试验组)。将植入前小鼠胚胎在这三种人血清和雌性大鼠血清(作为每个实验的内部对照)中培养,并评估其毒性(胚胎存活率)和致突变性(通过姐妹染色单体交换测定)。在有正常生殖史女性的血清和雌性大鼠血清中培养的胚胎,存活率分别为70.8±4.3%和78.9±0.9%。这两种血清类型的姐妹染色单体交换频率相似:15.7±0.2次姐妹染色单体交换/细胞(大鼠)和16.3±0.3次姐妹染色单体交换/细胞(人)。在补充有接受化疗女性血清的培养基中培养的小鼠胚胎,存活率显著降低(33.7±5.2%,P<0.01),且每个细胞的姐妹染色单体交换显著增加(26.5±0.6,P<0.01)。有生殖失败史女性的血清对植入前小鼠胚胎的影响是可变的且具有个体特异性。试验组约40%的女性血清产生的存活率和每个细胞的姐妹染色单体交换与接受化疗患者的血清相当。(摘要截短至250字)