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作 者:赵娜[1] 甄林青 胡启蒙[1] 王亮亮[1] 李新红[1]
机构地区:[1]上海交通大学农业与生物学院,上海市兽医生物技术重点实验室,上海200240
出 处:《畜牧兽医学报》2013年第11期1766-1774,共9页ACTA VETERINARIA ET ZOOTECHNICA SINICA
基 金:上海市科技兴农攻关项目(沪农科攻字2009第5-1号);上海市自然基金项目(ZR07150046)
摘 要:测定超低温冷冻保存过程能否诱导猪冻融精子产生"似凋亡"变化,探讨猪冻融精子活力降低的分子机理。利用Annexin-V/PI及JC-1荧光抗体试剂盒与流式细胞术相结合的方法,检测猪精子冷冻前后及不同培养时间冻融精子质膜中磷脂酰丝氨酸(PS)位置及线粒体膜电位(Δψm)变化;蛋白免疫印迹分析方法测定猪精子Bcl-2、Caspase-9及Caspase-3等"凋亡"因子含量变化。猪精子超低温冷冻保存后活性精子的比例(54.4%)显著低于鲜精组(87.9%)(P<0.05),其中PS移位的精子"似凋亡"比例约为26.8%,同鲜精组(5.6%)相比增加21.2个百分点(P<0.05);降温平衡及冷冻复苏后猪精子线粒体膜电位变化显著,其中低Δψm精子比例显著增加(P<0.05);同新鲜精子(19.6%)相比,冷冻复苏后(79.4%)低Δψm精子比例提高59.8个百分点(P<0.05);冻融精子中Bcl-2、Caspase-9及Caspase-3等凋亡因子活性显著高于鲜精子及降温平衡后的精子(P<0.05),由此证明冻融过程能诱导猪精子进入凋亡状态。超低温冷冻保存能导致猪冻融精子质膜磷脂酰丝氨酸(PS)移位及线粒体膜电位降低,同时激发精子Bcl-2、Caspase-9及Caspase-3等凋亡因子活性,诱导成活冻融精子提前进入"似凋亡"状态,明显缩短冻融精子存活时间,这可能是猪冻精繁殖力降低的又一诱因。The objective of the present work was to analyze whether cryopreservation could induce the "apoptosis-like" alteration of frozen-thawed boar sperm, and study the molecular mechanism of the fertility reduction of frozen-thawed sperm. Annexin-V/PI combined with the JC 1 fluores cence antibody Kit with flow cytometry (FCM) was used to determine the changes of phosphati dylserine (PS) location and mitochondrial membrane potential (△ψm) of boar sperm before and af- ter cryopreservation with different incubation times . Content changes of "apoptosis" factors(Bcl-2, Caspase-9 and Caspase-3)in boar sperm were validated by immunoblotting analysis. The results showed that the motility of the cryopreserved sperm (54. 4%) was lower than fresh sperm (87. 9%) (P 0.05), in which the percentage of "apoptosis-like" of sperm with PS dislocation (26.8%) was 21.2% higher(P〈0.05) than fresh sperm (5.6%). The cryopreservation caused an significant increase in the percentage of low Aq)m of equilibrated and cryopreserved sperm (P〈0.05). Com- pared with fresh sperm (19.6%), the percentage of sperm with low △ψm increased 59.8% after cryopreservation (P 〈0. 05). The activating levels of apoptotic factors (Bcl-2, Caspase-9 and Caspase-3)in cryopreserved sperm were remarkably higher than the fresh and equilibrated sperm (P〈0.05). Present evidences indicated that cryopreservation could induce spermatozoa into the "apoptosis-like" alteration. This study indicated that cryopreservation could not only lead to the dislocation of PS and reduced the mitochondrial membrane potential, but also stimulate the activi- ties of apoptotic factors (Bcl-2, Caspase-9 and Caspase-3), induce the frozen-thawed sperm into "apoptosis-like" state in advance, and shorten the survival time of frozen-thawed spermatozoa ob- viously. This might be another important reason for low pregnancy rate of frozen-thawed sperm.
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