Vadnais Melissa L, Cao Wenlei, Aghajanian Haig K, Haig-Ladewig Lisa, Lin Angel M, Al-Alao Osama, Gerton George L
Center for Research on Reproduction and Women's Health, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Center for Research on Reproduction and Women's Health, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania Department of Obstetrics and Gynecology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania
Biol Reprod. 2014 Jun;90(6):128. doi: 10.1095/biolreprod.113.114447. Epub 2014 Apr 16.
While most ATP, the main energy source driving sperm motility, is derived from glycolysis and oxidative phosphorylation, the metabolic demands of the cell require the efficient use of power stored in high-energy phosphate bonds. In times of high energy consumption, adenylate kinase (AK) scavenges one ATP molecule by transphosphorylation of two molecules of ADP, simultaneously yielding one molecule of AMP as a by-product. Either ATP or ADP supported motility of detergent-modeled cauda epididymal mouse sperm, indicating that flagellar AKs are functional. However, the ensuing flagellar waveforms fueled by ATP or ADP were qualitatively different. Motility driven by ATP was rapid but restricted to the distal region of the sperm tail, whereas ADP produced slower and more fluid waves that propagated down the full flagellum. Characterization of wave patterns by tracing and superimposing the images of the flagella, quantifying the differences using digital image analysis, and computer-assisted sperm analysis revealed differences in the amplitude, periodicity, and propagation of the waves between detergent-modeled sperm treated with either ATP or ADP. Surprisingly, addition of AMP to the incubation medium containing ATP recapitulated the pattern of sperm motility seen with ADP alone. In addition to AK1 and AK2, which we previously demonstrated are present in outer dense fibers and mitochondrial sheath of the mouse sperm tail, we show that another AK, AK8, is present in a third flagellar compartment, the axoneme. These results extend the known regulators of sperm motility to include AMP, which may be operating through an AMP-activated protein kinase.
虽然大多数驱动精子运动的主要能量来源ATP是由糖酵解和氧化磷酸化产生的,但细胞的代谢需求需要高效利用存储在高能磷酸键中的能量。在高能量消耗时,腺苷酸激酶(AK)通过将两分子ADP进行转磷酸化来 scavenges 一分子ATP,同时产生一分子AMP作为副产物。ATP或ADP都能支持去垢剂模拟的附睾尾小鼠精子的运动,这表明鞭毛中的AK具有功能。然而,由ATP或ADP驱动的后续鞭毛波形在性质上有所不同。由ATP驱动的运动速度很快,但仅限于精子尾部的远端区域,而ADP产生的波形较慢且更流畅,能沿着整个鞭毛传播。通过追踪和叠加鞭毛图像、使用数字图像分析量化差异以及计算机辅助精子分析来表征波形模式,结果显示用ATP或ADP处理的去垢剂模拟精子之间的波形在振幅、周期性和传播方面存在差异。令人惊讶的是,在含有ATP的孵育培养基中添加AMP可重现仅用ADP时观察到的精子运动模式。除了我们之前证明存在于小鼠精子尾部外致密纤维和线粒体鞘中的AK1和AK2外,我们还表明另一种AK,即AK8,存在于第三个鞭毛区室,即轴丝中。这些结果将已知的精子运动调节因子扩展到包括AMP,其可能通过AMP激活的蛋白激酶发挥作用。