Sari Luciana M, Zampini Renato, Gonzalez Del Pino Francisco, Argañaraz Martin E, Ratto Marcelo H, Apichela Silvana A
Facultad de Bioquímica, Química y Farmacia, Instituto Superior de Investigaciones Biológicas (INSIBIO), Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Instituto de Biología "Dr. Francisco D. Barbieri" Universidad Nacional de Tucumán (UNT), San Miguel de Tucumán, Argentina.
Cátedra de Biología Celular y Molecular, Facultad de Bioquímica, Química y Farmacia, Universidad Nacional de Tucumán, San Miguel de Tucumán, Argentina.
Front Vet Sci. 2021 Jan 5;7:610597. doi: 10.3389/fvets.2020.610597. eCollection 2020.
To provide new insights into the mechanisms through which seminal plasma proteins can protect sperm from damage caused during refrigeration, we evaluate the possibility that β-NGF can contribute to the improvement of sperm quality after cooling. First, β-NGF was detected in refrigerated sperm and compared with unrefrigerated sperm by western blotting of the proteins adsorbed by sperm, showing that native β-NGF is still present even 24 h after cooling only as an active form. Then, the effect of exogenous β-NGF on sperm quality after cooling was evaluated. A total of 12 ejaculates from male llamas (three ejaculates per male), were obtained by electro-ejaculation, diluted 4:1 with buffer Hepes-balanced salt solution and centrifuged at 800 × g for 8 min to remove the seminal plasma. Sperm were suspended in Tris-citrate-fructose-egg yolk diluent for a final concentration of 30 ×10/ml and cooled at 5°C for 24 h. After refrigeration, the extended sperm were equilibrated for 5 min at 37°C and divided into the following subgroups: sperm samples without treatment (control) and sperm samples supplemented with exogenous human β-NGF (10, 100, and 500 ng/ml). At 5, 30, and 60 min of incubation sperm were evaluated for sperm viability (using eosin/nigrosin stain), sperm motility and vigor (observed under light microscopy), and mitochondrial activity (using the JC-1 fluorescent marker). Vigor data were analyzed with the nonparametric Kruskal-Wallis test. The rest of the variables were analyzed with a mixed models approach. Mean comparisons were performed using Fisher's LSD test with a confidence level of 95%. A principal components analysis was performed to analyze the relationships between variables. Treatment of 24 h cooled sperm with 10 or 100 ng/ml of human β-NGF increased the percentage of total motility and vigor ( < 0.05). Besides, an incubation time of 60 min would be adequate to improve sperm quality, since all variables are positively related. The significant improvement observed in the motility and vigor of post-refrigerated sperm suggests that supplementation with exogenous β-NGF may be profitable for the improvement of cooled llama sperm.
为了深入了解精浆蛋白保护精子免受冷藏过程中损伤的机制,我们评估了β-神经生长因子(β-NGF)有助于改善精子冷却后质量的可能性。首先,通过对精子吸附的蛋白质进行蛋白质免疫印迹,在冷藏精子中检测β-NGF,并与未冷藏精子进行比较,结果表明,即使在冷却24小时后,天然β-NGF仍以活性形式存在。然后,评估外源性β-NGF对精子冷却后质量的影响。通过电刺激射精从雄性美洲驼中获取总共12份精液(每只雄性3份精液),用缓冲的Hepes平衡盐溶液按4:1稀释,并以800×g离心8分钟以去除精浆。将精子悬浮在柠檬酸-果糖-蛋黄稀释液中,最终浓度为30×10⁶/ml,并在5°C下冷却24小时。冷藏后,将稀释后的精子在37°C下平衡5分钟,并分为以下亚组:未处理的精子样本(对照)和补充外源性人β-NGF(10、100和500 ng/ml)的精子样本。在孵育5、30和60分钟时,评估精子活力(使用伊红/黑色素染色)、精子运动能力和活力(在光学显微镜下观察)以及线粒体活性(使用JC-1荧光标记)。活力数据采用非参数Kruskal-Wallis检验进行分析。其余变量采用混合模型方法进行分析。使用Fisher最小显著差异检验进行均值比较,置信水平为95%。进行主成分分析以分析变量之间的关系。用10或100 ng/ml的人β-NGF处理冷却24小时的精子可提高总运动能力和活力的百分比(P<0.05)。此外,60分钟的孵育时间足以改善精子质量,因为所有变量均呈正相关。冷藏后精子运动能力和活力的显著改善表明,补充外源性β-NGF可能有利于改善冷却后的美洲驼精子质量。