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Protein tyrosine phosphorylation and zona binding ability of in vitro capacitated and cryopreserved buffalo spermatozoa

机译:水牛精子和冷冻保存的水牛精子的蛋白酪氨酸磷酸化和透明带结合能力

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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 mu g/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
机译:已经证明,与正常容量和冷冻剂量相关的变化之间有许多相似之处。进行本研究以确定在体外酪蛋白化(肝素诱导; 20微克/毫升)和冻融(冷冻)的水牛精子蛋白酪氨酸磷酸化模式和透明带结合能力之间是否存在相似性。将来自七头水牛公牛的精液(每支八粒射精)分为两部分。第一部分用作新鲜精液,第二部分在Tris-蛋黄补充剂中扩展,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了含磷酸酪氨酸的蛋白质的定位。对于透明带结合测定,使用了通过抽吸技术从新鲜的水牛卵巢中收集到的高质量卵母细胞。结合的精子用Hoechst 33342染料染色并在荧光显微镜下观察。结果显示在体外获能和冻融的精子中,精子头部相关蛋白酪氨酸磷酸化。在透明带结合试验中,在非精子培养基中分别于0 h和3 h孵育后,新鲜精液中结合精子的平均数分别为90.6 +/- 1.9和104.7 +/- 2.2。但是在电容性介质中与肝素一起孵育3小时后,附着在透明带上的精子的平均数量为138.4 +/- 2.6。体外获能的精子比新鲜精子具有明显更高的结合能力(P <0.05)。冷冻和解冻后,冷冻保存的精子的透明带结合力与体外能力的精子相比降低了2.5倍。体外获能的精子的结合能力显着(P <0.01)高于冷冻融化(冷冻定性)的精子。研究得出结论,体外获能和冻融(冷冻定性)的精子均具有相似的酪氨酸磷酸化蛋白模式的免疫定位,但是在透明带结合能力上却有所不同

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