Fukuda A, Roudebush W E, Thatcher S S
Department of Obstetrics and Gynecology, James H. Quillen College of Medicine, East Tennessee State University, Johnson City 37614-0569.
J Assist Reprod Genet. 1992 Aug;9(4):378-83. doi: 10.1007/BF01203963.
Our purpose was to investigate the influence of in vitro oocyte aging on fertilization and subsequent embryonic development following subzonal sperm injection with reference to spontaneous zona hardening in the mouse.
First cleavage rate was significantly higher in long vs short (69 vs 41%, P < 0.001). However, significantly higher blastocyst formation and hatching were observed in short than long (50 vs 7%, P < 0.001, and 86 vs 50%, P < 0.001, respectively). No significant differences were found for two pronuclei formation between short and long (30 vs 27%). Sham injection revealed a significantly higher parthenogenetic activation in long than short (19 vs 2%, P < 0.001). Zona digestion required a significantly longer time for long compared to short (trypsin--37 vs 29 min, P < 0.01; pronase--17 vs 14 min, P < 0.001).
Prolonged culture of mature mouse oocytes in vitro alters the zona pellucida, increases the rate of parthenogenetic activation by subzonal sperm injection, and impairs subsequent embryonic development. Zona hardening appears to be an indicator of oocyte aging.
我们的目的是参照小鼠自发透明带硬化,研究体外卵母细胞老化对卵母细胞内单精子注射后受精及后续胚胎发育的影响。
长时培养组的首次卵裂率显著高于短时培养组(69%对41%,P<0.001)。然而,短时培养组的囊胚形成率和孵化率显著高于长时培养组(分别为50%对7%,P<0.001;86%对50%,P<0.001)。短时和长时培养组的双原核形成率无显著差异(30%对27%)。假注射显示长时培养组的孤雌激活率显著高于短时培养组(19%对2%,P<0.001)。与短时培养相比,长时培养的透明带消化所需时间显著更长(胰蛋白酶——37分钟对29分钟,P<0.01;链霉蛋白酶——17分钟对14分钟,P<0.001)。
成熟小鼠卵母细胞体外长时间培养会改变透明带,增加卵母细胞内单精子注射的孤雌激活率,并损害后续胚胎发育。透明带硬化似乎是卵母细胞老化的一个指标。