Wang H X, Flaherty S P, Swann N J, Matthews C D
Department of Obstetrics and Gynaecology, University of Adelaide, Queen Elizabeth Hospital, Woodville, Australia.
Hum Reprod. 1994 Jul;9(7):1265-70. doi: 10.1093/oxfordjournals.humrep.a138692.
The aim of this study was to evaluate the efficacy of enriching X-bearing human spermatozoa using 12-step (25-80%) discontinuous Percoll gradients. X- and Y-bearing spermatozoa were simultaneously identified in neat semen (controls) and in 80% Percoll fractions from the same samples using double-label fluorescence in-situ hybridization and chromosome-specific DNA probes. Hybridization and labelling efficiencies of 95-99% were obtained in all samples. The mean ratio of X- to Y-bearing spermatozoa in the controls was 49.0:48.2, whereas there was a significant enrichment (P < 0.0001) of X-bearing spermatozoa in the Percoll fractions (mean X:Y ratio was 55.1:41.1 or 1.35). The ratio varied from 1.1-1.5 in individual Percoll samples. There were no significant differences in the proportions of aneuploid spermatozoa (XX, YY, XY) between the control and Percoll fractions. We conclude that 12-step discontinuous Percoll gradients enrich X-bearing spermatozoa, but the degree of enrichment is insufficient for use in preconceptional sex selection.
本研究的目的是评估使用12步(25%-80%)不连续Percoll梯度富集携带X染色体的人类精子的效果。使用双标记荧光原位杂交和染色体特异性DNA探针,在纯精液(对照)和相同样本的80%Percoll组分中同时鉴定携带X和Y染色体的精子。所有样本的杂交和标记效率均达到95%-99%。对照中携带X染色体与携带Y染色体精子的平均比例为49.0:48.2,而在Percoll组分中携带X染色体的精子有显著富集(P<0.0001)(平均X:Y比例为55.1:41.1或1.35)。在各个Percoll样本中,该比例在1.1-1.5之间变化。对照和Percoll组分中非整倍体精子(XX、YY、XY)的比例没有显著差异。我们得出结论,12步不连续Percoll梯度可富集携带X染色体的精子,但富集程度不足以用于孕前性别选择。