Wandernoth Petra M, Mannowetz Nadja, Szczyrba Jaroslaw, Grannemann Laura, Wolf Anne, Becker Holger M, Sly William S, Wennemuth Gunther
From the Institute of Anatomy, University Hospital, University Duisburg-Essen, Hufelandstraße 55, 45122 Essen, Germany.
the Department of Internal Medicine I, Saarland University Medical Center, Kirrberger Straße, 66421 Homburg/Saar, Germany.
J Biol Chem. 2015 Dec 4;290(49):29202-16. doi: 10.1074/jbc.M115.698597. Epub 2015 Oct 20.
HCO3 (-) is a key factor in the regulation of sperm motility. High concentrations of HCO3 (-) in the female genital tract induce an increase in sperm beat frequency, which speeds progress of the sperm through the female reproductive tract. Carbonic anhydrases (CA), which catalyze the reversible hydration of CO2 to HCO3 (-), represent potential candidates in the regulation of the HCO3 (-) homeostasis in sperm and the composition of the male and female genital tract fluids. We show that two CA isoforms, CAII and CAIV, are distributed along the epididymal epithelium and appear with the onset of puberty. Expression analyses reveal an up-regulation of CAII and CAIV in the different epididymal sections of the knockout lines. In sperm, we find that CAII is located in the principal piece, whereas CAIV is present in the plasma membrane of the entire sperm tail. CAII and CAIV single knockout animals display an imbalanced HCO3 (-) homeostasis, resulting in substantially reduced sperm motility, swimming speed, and HCO3 (-)-enhanced beat frequency. The CA activity remaining in the sperm of CAII- and CAIV-null mutants is 35% and 68% of that found in WT mice. Sperm of the double knockout mutant mice show responses to stimulus by HCO3 (-) or CO2 that were delayed in onset and reduced in magnitude. In comparison with sperm from CAII and CAIV double knockout animals, pharmacological loss of CAIV in sperm from CAII knockout animals, show an even lower response to HCO3 (-). These results suggest that CAII and CAIV are required for optimal fertilization.
HCO3(-)是精子活力调节的关键因素。雌性生殖道中高浓度的HCO3(-)会导致精子搏动频率增加,从而加快精子在雌性生殖道中的前进速度。碳酸酐酶(CA)催化CO2可逆水合生成HCO3(-),是精子中HCO3(-)稳态以及雄性和雌性生殖道液成分调节的潜在候选因子。我们发现两种CA同工型,CAII和CAIV,沿附睾上皮分布,并在青春期开始时出现。表达分析显示敲除系不同附睾节段中CAII和CAIV上调。在精子中,我们发现CAII位于主段,而CAIV存在于整个精子尾部的质膜中。CAII和CAIV单敲除动物表现出HCO3(-)稳态失衡,导致精子活力、游动速度和HCO3(-)增强的搏动频率大幅降低。CAII和CAIV基因敲除突变体精子中剩余的CA活性分别为野生型小鼠的35%和68%。双敲除突变体小鼠的精子对HCO3(-)或CO2刺激的反应在起始时间上延迟且幅度降低。与CAII和CAIV双敲除动物的精子相比,CAII敲除动物精子中CAIV的药理学缺失对HCO3(-)的反应更低。这些结果表明CAII和CAIV是最佳受精所必需的。