Indian Veterinary Research Institute, Izatnagar, India.
Theriogenology. 2011 Jun;75(9):1630-9. doi: 10.1016/j.theriogenology.2011.01.003. Epub 2011 Mar 31.
Many similarities between the changes associated with normal capacitation and cryocapacitation have been demonstrated. The present study was undertaken to determine whether similarities exist in the protein tyrosine phosphorylation pattern and zona binding ability between in vitro capacitated (heparin induced; 20 μg/ml) and frozen-thawed (cryocapacitated) buffalo spermatozoa. Semen from seven buffalo bulls (eight ejaculates each) was divided into two parts. Part I was used as fresh semen and part II was extended in Tris-egg yolk extender, equilibrated and frozen in liquid nitrogen. Localization of phosphotyrosine-containing protein was determined using an indirect immunoflourescence assay with anti-phosphotyrosine antibody. For zona binding assay, good quality oocytes collected by aspiration technique from fresh buffalo ovaries were used. The bound spermatozoa were stained with Hoechst 33342 dye and observed under fluorescent microscope. The results revealed sperm head associated protein tyrosine phosphorylation in both in vitro capacitated and frozen-thawed spermatozoa. In the zona binding assay, the mean number of bound spermatozoa was 90.6 ± 1.9 and 104.7 ± 2.2 in fresh semen after incubation in non capacitating media at 0 h and 3 h, respectively. But after incubation in capacitating media with heparin for 3 h, the mean number of spermatozoa attached to zona pellucida was 138.4 ± 2.6. The in vitro capacitated spermatozoa had significantly (P < 0.05) higher binding ability than that of fresh spermatozoa. After freezing and thawing, 2.5 fold reductions in the zona binding ability of cryopreserved spermatozoa was observed compared to in vitro capacitated spermatozoa. The binding ability of in vitro capacitated spermatozoa was significantly (P < 0.01) higher than that of frozen-thawed (cryocapacitated) spermatozoa. The study concluded that both in vitro capacitated and frozen-thawed (cryocapacitated) spermatozoa had similar immune-localization of tyrosine phosphorylated protein pattern, however, differed in the zona binding ability.
许多与正常获能相关的变化之间存在相似性,并且已经证明与冷冻获能之间存在相似性。本研究旨在确定体外获能(肝素诱导;20μg/ml)和冷冻解冻(冷冻获能)水牛精子之间的酪氨酸磷酸化模式和透明带结合能力是否存在相似性。来自七头水牛公牛(每个公牛 8 个精液样本)的精液分为两部分。第一部分用作新鲜精液,第二部分用 Tris-卵黄稀释液扩展,平衡并在液氮中冷冻。使用抗磷酸酪氨酸抗体的间接免疫荧光测定法确定含磷酸酪氨酸的蛋白质的定位。对于透明带结合测定,使用从新鲜水牛卵巢中抽吸技术收集的优质卵母细胞。将结合的精子用 Hoechst 33342 染料染色,并在荧光显微镜下观察。结果表明,体外获能和冷冻解冻的精子均存在精子头相关的蛋白酪氨酸磷酸化。在透明带结合测定中,在非获能培养基中孵育 0 小时和 3 小时后,新鲜精液中结合的精子的平均数量分别为 90.6±1.9 和 104.7±2.2。但是,在用肝素在获能培养基中孵育 3 小时后,附着在透明带的精子数平均为 138.4±2.6。体外获能的精子比新鲜精子具有更高的结合能力,差异有统计学意义(P<0.05)。冷冻和解冻后,冷冻保存的精子的透明带结合能力比体外获能的精子降低了 2.5 倍。体外获能的精子的结合能力明显高于冷冻解冻(冷冻获能)的精子(P<0.01)。该研究得出结论,体外获能和冷冻解冻(冷冻获能)的精子均具有相似的酪氨酸磷酸化蛋白模式的免疫定位,但在透明带结合能力上存在差异。