The Research Institute of the McGill University Health Centre, Montreal, QC, Canada.
Department of Surgery (Urology Division), McGill University, Montréal, QC, Canada.
Hum Reprod. 2018 Aug 1;33(8):1394-1407. doi: 10.1093/humrep/dey221.
Are all components of the peroxiredoxins (PRDXs) system important to control the levels of reactive oxygen species (ROS) to maintain viability and DNA integrity in spermatozoa?
PRDX6 is the primary player of the PRDXs system for maintaining viability and DNA integrity in human spermatozoa.
Mammalian spermatozoa are sensitive to high levels of ROS and PRDXs are antioxidant enzymes proven to control the levels of ROS generated during sperm capacitation to avoid oxidative damage in the spermatozoon. Low amounts of PRDXs are associated with male infertility. The absence of PRDX6 promotes sperm oxidative damage and infertility in mice.
STUDY DESIGN, SIZE, DURATION: Semen samples were obtained over a period of one year from a cohort of 20 healthy non-smoking volunteers aged 22-30 years old.
PARTICIPANTS/MATERIALS, SETTING, METHODS: Sperm from healthy donors was incubated for 2 h in the absence or presence of inhibitors for the 2-Cys PRDXs system (peroxidase, reactivation system and NADPH-enzymes suppliers) or the 1-Cys PRDX system (peroxidase and calcium independent-phospholipase A2 (Ca2+-iPLA2) activity). Sperm viability, DNA oxidation, ROS levels, mitochondrial membrane potential and 4-hydroxynonenal production were determined by flow cytometry.
We observed a significant decrease in viable cells due to inhibitors of the 2-Cys PRDXs, PRDX6 Ca2+-iPLA2 activity or the PRDX reactivation system compared to controls (P ≤ 0.05). PRDX6 Ca2+-iPLA2 activity inhibition had the strongest detrimental effect on sperm viability and DNA oxidation compared to controls (P ≤ 0.05). The 2-Cys PRDXs did not compensate for the inhibition of PRDX6 peroxidase and Ca2+-iPLA2 activities.
Not applicable.
LIMITATIONS, REASONS FOR CAUTION: Players of the reactivation systems may differ among mammalian species.
The Ca2+-iPLA2 activity of PRDX6 is the most important and first line of defense against oxidative stress in human spermatozoa. Peroxynitrite is scavenged mainly by the PRDX6 peroxidase activity. These findings can help to design new diagnostic tools and therapies for male infertility.
STUDY FUNDING/COMPETING INTEREST(S): This research was supported by The Canadian Institutes of Health Research (MOP 133661 to C.O.), and by RI MUHC-Desjardins Studentship in Child Health Research awarded to M.C.F. The authors have nothing to disclose.
过氧化物酶(PRDXs)系统的所有成分对于控制活性氧(ROS)水平以维持精子活力和 DNA 完整性是否都很重要?
PRDX6 是 PRDXs 系统在维持人类精子活力和 DNA 完整性方面的主要参与者。
哺乳动物精子对高水平的 ROS 很敏感,而 PRDXs 是已被证明可控制精子获能过程中产生的 ROS 水平以避免精子内氧化损伤的抗氧化酶。PRDXs 的含量低与男性不育有关。PRDX6 的缺失会促进精子的氧化损伤并导致小鼠不育。
研究设计、规模、持续时间:在一年的时间里,从 20 名年龄在 22-30 岁的健康非吸烟志愿者的队列中获得了精液样本。
参与者/材料、设置、方法:将健康供体的精子在不存在或存在 2-Cys PRDXs 系统(过氧化物酶、再激活系统和 NADPH-酶供应商)或 1-Cys PRDX 系统(过氧化物酶和钙非依赖性磷脂酶 A2(Ca2+-iPLA2)活性抑制剂的情况下孵育 2 小时。通过流式细胞术测定精子活力、DNA 氧化、ROS 水平、线粒体膜电位和 4-羟基壬烯醛的产生。
与对照组相比,我们观察到 2-Cys PRDXs、PRDX6 Ca2+-iPLA2 活性或 PRDX 再激活系统的抑制剂显著降低了有活力的细胞(P≤0.05)。与对照组相比,PRDX6 Ca2+-iPLA2 活性抑制剂对精子活力和 DNA 氧化的抑制作用最强(P≤0.05)。2-Cys PRDXs 不能补偿 PRDX6 过氧化物酶和 Ca2+-iPLA2 活性的抑制作用。
不适用。
局限性、谨慎的原因:哺乳动物物种之间的再激活系统的参与者可能不同。
PRDX6 的 Ca2+-iPLA2 活性是人类精子中对抗氧化应激的最重要和第一道防线。过氧亚硝酸盐主要由 PRDX6 过氧化物酶活性清除。这些发现有助于设计男性不育症的新诊断工具和治疗方法。
研究资金/竞争利益:本研究由加拿大健康研究所(MOP 133661 给 C.O.)和 RI MUHC-Desjardins 儿童健康研究奖学金(授予 M.C.F.)支持。作者没有任何利益冲突。