氧化磷酸化而不是糖酵解是贻贝精子运动的主要能量来源。

IF 1.9 3区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Hui Kong , Inna M. Sokolova
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引用次数: 0

摘要

繁殖的海洋贻贝依靠高精子活力在动态海水环境中成功受精。线粒体通常被认为是通过氧化磷酸化(OXPHOS)产生ATP的主要来源;然而,贻贝精子的ATP生成途径尚未完全表征。为了更好地理解OXPHOS和糖酵解对贻贝精子功能的重要性,我们在贻贝精子中进行了抑制这些途径的实验。我们的研究结果表明,寡霉素,一种线粒体ATP合成酶的抑制剂,可以立即降低精子的运动率、速度和ATP含量,而2-脱氧-d-葡萄糖,一种糖酵解抑制剂,没有效果。OXPHOS抑制剂鱼藤酮也部分降低了精子的运动率和速度。有趣的是,没有发现抑制剂对贻贝精子中富含能量的化合物(脂质、碳水化合物和蛋白质)含量有影响的证据,这表明只有适度的能量需求来促进精子运动。基于这些发现,我们得出结论,OXPHOS是海洋贻贝精子运动的主要能量来源。我们的研究揭示了贻贝精子生理学的复杂性,并强调了了解广播产卵海洋无脊椎动物成功受精所需能量的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Oxidative phosphorylation rather than glycolysis is the primary energy source for sperm motility in the mussels Mytilus edulis

Oxidative phosphorylation rather than glycolysis is the primary energy source for sperm motility in the mussels Mytilus edulis

Broadcast-spawning marine mussels rely on high sperm motility for successful fertilization in the dynamic seawater environment. Mitochondria are typically considered the primary source of ATP generation via oxidative phosphorylation (OXPHOS); however, the ATP generation pathways of mussel sperm have not been fully characterized. To better understand the importance of both OXPHOS and glycolysis for mussel sperm function, we conducted experiments inhibiting these pathways in sperm from Mytilus edulis. Our results indicate that oligomycin, an inhibitor of the mitochondrial ATP synthase, immediately decreased sperm motility rate, velocity, and ATP content, while 2-deoxy-d-glucose, a glycolysis inhibitor, had no effect. The OXPHOS inhibitor rotenone also partially reduced sperm motility rate and velocity. Interestingly, no evidence was found for the inhibitors' effects on the content of energy-rich compounds (lipids, carbohydrates, and proteins) in the mussels' sperm, indicating only modest energy demand to fuel sperm motility. Based on these findings, we conclude that OXPHOS is the primary energy source for sperm motility in marine mussels. Our study sheds light on the intricacies of mussel sperm physiology and highlights the importance of understanding the energy requirements for successful fertilization in broadcast-spawning marine invertebrates.

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来源期刊
CiteScore
4.60
自引率
4.50%
发文量
77
审稿时长
22 days
期刊介绍: Comparative Biochemistry & Physiology (CBP) publishes papers in comparative, environmental and evolutionary physiology. Part B: Biochemical and Molecular Biology (CBPB), focuses on biochemical physiology, primarily bioenergetics/energy metabolism, cell biology, cellular stress responses, enzymology, intermediary metabolism, macromolecular structure and function, gene regulation, evolutionary genetics. Most studies focus on biochemical or molecular analyses that have clear ramifications for physiological processes.
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