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Signaling in sperm: toward a molecular understanding of the acquisition of sperm motility in the mouse epididymis.精子中的信号转导:对小鼠附睾中精子运动能力获得的分子理解。
Biol Reprod. 2013 Nov 27;89(5):127. doi: 10.1095/biolreprod.113.110163. Print 2013 Nov.
2
AMP-activated kinase, AMPK, is involved in the maintenance of plasma membrane organization in boar spermatozoa.AMP激活蛋白激酶(AMPK)参与维持公猪精子质膜的组织结构。
Biochim Biophys Acta. 2013 Sep;1828(9):2143-51. doi: 10.1016/j.bbamem.2013.05.026. Epub 2013 Jun 4.
3
Disruption of a spermatogenic cell-specific mouse enolase 4 (eno4) gene causes sperm structural defects and male infertility.生精细胞特异性小鼠烯醇酶 4(eno4)基因的破坏导致精子结构缺陷和男性不育。
Biol Reprod. 2013 Apr 11;88(4):90. doi: 10.1095/biolreprod.112.107128. Print 2013 Apr.
4
New adenylate kinase 7 (AK7) mutation in primary ciliary dyskinesia.原发性纤毛运动障碍中的新腺苷酸激酶 7(AK7)突变。
Am J Rhinol Allergy. 2012 Jul-Aug;26(4):260-4. doi: 10.2500/ajra.2012.26.3784.
5
AMP-activated kinase AMPK is expressed in boar spermatozoa and regulates motility.AMP 激活的蛋白激酶 AMPK 在猪精子中表达并调节其运动能力。
PLoS One. 2012;7(6):e38840. doi: 10.1371/journal.pone.0038840. Epub 2012 Jun 14.
6
ATP-activated P2X2 current in mouse spermatozoa.ATP 激活的 P2X2 电流在小鼠精子中。
Proc Natl Acad Sci U S A. 2011 Aug 23;108(34):14342-7. doi: 10.1073/pnas.1111695108. Epub 2011 Aug 10.
7
Congenital hydrocephalus in genetically engineered mice.先天性脑积水在基因工程小鼠中。
Vet Pathol. 2012 Jan;49(1):166-81. doi: 10.1177/0300985811415708. Epub 2011 Jul 11.
8
Ion channels, phosphorylation and mammalian sperm capacitation.离子通道、磷酸化和哺乳动物精子获能。
Asian J Androl. 2011 May;13(3):395-405. doi: 10.1038/aja.2010.69.
9
Role of adenylate kinase type 7 expression on cilia motility: possible link in primary ciliary dyskinesia.腺嘌呤激酶 7 型表达在纤毛运动中的作用:原发性纤毛运动障碍的可能联系。
Am J Rhinol Allergy. 2010 May-Jun;24(3):181-5. doi: 10.2500/ajra.2010.24.3468.
10
AMPK-mediated regulation of transcription in skeletal muscle.AMPK 介导的骨骼肌转录调控。
Clin Sci (Lond). 2010 Jan 26;118(8):507-18. doi: 10.1042/CS20090533.

腺嘌呤核苷酸代谢及AMP在调节小鼠精子鞭毛波形中的作用。

Adenine nucleotide metabolism and a role for AMP in modulating flagellar waveforms in mouse sperm.

作者信息

Vadnais Melissa L, Cao Wenlei, Aghajanian Haig K, Haig-Ladewig Lisa, Lin Angel M, Al-Alao Osama, Gerton George L

机构信息

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

出版信息

Biol Reprod. 2014 Jun;90(6):128. doi: 10.1095/biolreprod.113.114447. Epub 2014 Apr 16.

DOI:10.1095/biolreprod.113.114447
PMID:24740601
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4094002/
Abstract

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.

摘要

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。