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A 31-kDa seminal plasma heparin-binding protein reduces cold shock stress during cryopreservation of cross-bred cattle bull semen

机译:31-KDA精液肝素结合蛋白在跨繁殖牛牛仔精液的冷冻保存期间减少了冷震胁迫

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In the present study, a 31-kDa protein, purified from cattle bull seminal plasma heparin binding proteins (SP-HBP), was characterized by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and mass spectrometry. Raw semen of six cross-bred bulls was treated with 31-kDa HBP before cryopreservation to observe its effect on motility, viability, hypo-osmotic swelling test, acrosome integrity, in vitro capacitation/acrosome reaction, and oxidative stress at pre-freeze and frozen-thawed phases of cryopreservation. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis of 31-kDa protein eluted and purified from SP-HBP (separated on acrylamide gels) resulted in a single band of 40 kDa. In matrix-assisted laser desorption/ionization-time of flight analysis, 12 peptides were identified with matching significantly (P 0.05) to interlukin-6 of bovine with a top score of 55. Addition of 25 mu g/mL of fluorescein isothiocyanate-conjugated 31-kDa protein to raw semen and incubation at 37 degrees C for 20 minutes before cryopreservation resulted in its binding mainly to head region. Treatment of semen with 31-kDa HBP resulted in a significant (P 0.05) average increase of 9.2%, 6.8%, and 11.7% and 5.5%, 6.5%, and 11.0% in motile, viable, hypo-osmotic swelling-responsive spermatozoa in six bulls at pre-freeze and frozen-thawed phases of cryopreservation, respectively. Percentage of spermatozoa with intact acrosomes nonsignificantly enhanced in the semen treated with 31-kDa HBP at both phases of cryopreservation. An average nonsignificant increase of 3.1% in in vitro capacitated and acrosome-reacted spermatozoa was obtained in semen supplemented with 31-kDa HBP. Addition of 31-kDa HBP also nonsignificantly reduced Malonadialdehyde (MDA) level by 10.7 and 19.3 mu M/10(9) spermatozoa in prefrozen and frozen-thawed semen, respectively. The results obtained here indicate to conclude that treatment of cross-bred cattle bull semen with 31-kDa HBP protects the spermatozoa from cold shock effect by coating the sperm surface. (C) 2016 Elsevier Inc. All rights reserved.
机译:在本研究中,通过十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳和质谱,从牛牛精液肝素结合蛋白(SP-HBP)中纯化的31kDa蛋白质。在冷冻保存前用31 kda hbp治疗六个杂交公牛的原始精液,观察其对预冻结和预冻结的运动,活力,低渗透肿胀试验,副高剂量的完整性,体外电容和氧化胁迫的影响冷冻保存的冷冻阶段。硫酸钠 - 聚丙烯酰胺凝胶电泳的31-KDA蛋白质洗脱并从SP-HBP(在丙烯酰胺凝胶上分离)产生,导致单带40kDa。在基质辅助激光解吸/电离 - 飞行时间分析中,用顶分为55的匹配显着(P <0.05)匹配12种肽(P <0.05)。添加25μg/ ml异硫氰酸酯的荧光素 - 将31-KDA蛋白质到粗精液,并在37℃下孵育20分钟,然后冷冻保存导致其主要与头部区域的结合。用31-KDA HBP处理精液产生显着(P <0.05)的平均增加9.2%,6.8%和11.7%和5.5%,6.5%,6.0%,可行,可行,渗透肿胀 - 在六公牛队分别在六公牛的六分之一的冷冻保存阶段进行敏感精子。在用31-KDA HBP在冷冻保存的两相处理的精液中,具有完整辅助体的精子与完整辅助物的百分比。在补充有31-KDA HBP的精液中获得体外电容和取饰反应的精子3.1%的平均无显着性增加3.1%。添加31-KDA HBP,也分别在替代和冷冻解冻的精液中减少了10.7和19.3μm/ 10(9)个精子的Malonadialdehyde(MDA)水平。此处获得的结果表明,通过涂覆精子表面来得出与31-KDA HBP的交叉牛牛仔精液的处理保护精子免受冷冲击效果。 (c)2016年Elsevier Inc.保留所有权利。

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