Keefer C L, Younis A I, Brackett B G
Department of Physiology and Pharmacology, College of Veterinary Medicine, University of Georgia, Athens.
Mol Reprod Dev. 1990 Mar;25(3):281-5. doi: 10.1002/mrd.1080250310.
Whole in vitro capacitated bovine spermatozoa were microinjected directly into the ooplasm of in vitro matured bovine oocytes in order to determine whether oocytes fertilized by sperm injection could undergo normal pronuclear formation and cleavage development. Immature oocytes recovered from follicles (2-5 mm) of unstimulated ovaries were cultured for 24-25 h in modified TCM 199 medium supplemented with heat-treated day 20 cow serum, luteinizing hormone (LH), and estradiol 17-B. In vitro capacitated, frozen-thawed spermatozoa were injected into the ooplasm, and the injected oocytes were cultured for an additional 24-28 h. Twenty-one percent (21/101) of the sperm-injected oocytes contained a sperm within the ooplasm; however, only 2% (2/101) cleaved. The remaining oocytes either did not contain a sperm or had degenerated. After oocyte activation induced by a 5 min incubation in 1 microM A23187, sperm nuclear decondensation occurred in the A23187-activated, injected oocytes but not in the unactivated, injected controls (37% vs. 0% after 3 h). Those injected, activated oocytes that contained a male pronucleus also exhibited a female pronucleus and second polar body. Furthermore, a significantly higher number (28%, 6/21) of the injected, activated oocytes cleaved to a two- to four-cell stage after 48 h than did the injected, unactivated oocytes (4%). These results indicate that, unlike hamster and rabbit oocytes, bovine oocytes are not sufficiently stimulated by the injection procedure to complete meiosis, but, upon activation by calcium ionophore, they will undergo normal-appearing cleavage development following fertilization by sperm injection.
将体外完全获能的牛精子直接显微注射到体外成熟的牛卵母细胞的卵质中,以确定通过精子注射受精的卵母细胞是否能够进行正常的原核形成和卵裂发育。从未经刺激的卵巢的卵泡(2 - 5毫米)中回收的未成熟卵母细胞,在添加了经热处理的第20天牛血清、促黄体生成素(LH)和雌二醇17 - B的改良TCM 199培养基中培养24 - 25小时。将体外获能、冻融的精子注射到卵质中,注射后的卵母细胞再培养24 - 28小时。21%(21/101)的精子注射卵母细胞的卵质内含有精子;然而,只有2%(2/101)发生了卵裂。其余的卵母细胞要么不含精子,要么已经退化。在1 microM A23187中孵育5分钟诱导卵母细胞激活后,A23187激活的注射卵母细胞中发生了精子核去浓缩,而未激活的注射对照中未发生(3小时后分别为37%和0%)。那些含有雄原核的注射激活卵母细胞也显示出雌原核和第二极体。此外,48小时后,注射激活的卵母细胞中有显著更多数量(28%,6/21)分裂到二至四细胞阶段,而注射未激活的卵母细胞中这一比例为4%。这些结果表明,与仓鼠和兔卵母细胞不同,牛卵母细胞未被注射操作充分刺激以完成减数分裂,但是,在钙离子载体激活后,它们在通过精子注射受精后将经历外观正常的卵裂发育。