O'Flaherty Cristian
Departments of Surgery (Urology Division) and Pharmacology and Therapeutics, Faculty of Medicine, McGill University and the Research Institute, McGill University Health Centre, Montréal, QC H4A 3J1, Canada.
Antioxidants (Basel). 2018 Nov 24;7(12):173. doi: 10.3390/antiox7120173.
The spermatozoon is a terminal cell with the unique purpose of delivering the paternal genome to the oocyte during fertilization. Once spermatozoa enter into the female reproductive tract, they count on only the antioxidant protection that they received during spermatogenesis and epididymal maturation. Peroxiredoxins (PRDXs), particularly PRDX6, are important players in the antioxidant protection and regulation of reactive oxygen species (ROS) levels in spermatozoa. PRDX6, through its peroxidase and calcium-independent phospholipase A₂ activities, plays a major role in the regulation of ROS to maintain viability and motility and allow the spermatozoon to achieve fertilizing ability during the complex process of capacitation. The absence of PRDX6 is sufficient to promote abnormal reproductive outcomes in mice that resemble what we observe in infertile men. Indeed, Prdx6 spermatozoa display low motility and severe DNA damage, which is translated into reduced ability to fertilize oocytes in vitro or produce a low number of pups compared to wild-type controls. This review focuses on the role of PRDX6 as the primary antioxidant enzyme that protects the spermatozoon from oxidative-stress-associated damages to protect the paternal genome and assure fertility.
精子是一种终末细胞,其独特功能是在受精过程中将父本基因组传递给卵母细胞。精子一旦进入雌性生殖道,就只能依靠在精子发生和附睾成熟过程中获得的抗氧化保护。过氧化物酶(PRDXs),尤其是PRDX6,在精子的抗氧化保护和活性氧(ROS)水平调节中起着重要作用。PRDX6通过其过氧化物酶和钙非依赖性磷脂酶A₂活性,在调节ROS以维持精子活力和运动能力方面发挥主要作用,并使精子在复杂的获能过程中获得受精能力。PRDX6的缺失足以在小鼠中导致异常的生殖结果,类似于我们在不育男性中观察到的情况。事实上,与野生型对照相比,Prdx6基因缺失的精子表现出低运动能力和严重的DNA损伤,这导致其体外受精能力下降或产仔数减少。本综述重点关注PRDX6作为主要抗氧化酶的作用,它保护精子免受氧化应激相关损伤,以保护父本基因组并确保生育能力。