Advancing age increases sperm chromatin damage and impairs fertility in peroxiredoxin 6 null mice

精子 生育率 男科 生物 DNA断裂 精子活力 染色质 生理学 遗传学 人口学 医学 人口 细胞凋亡 程序性细胞死亡 DNA 社会学
作者
Burak Özkösem,Sheldon I. Feinstein,Aron B. Fisher,Cristián O’Flaherty
出处
期刊:Redox biology [Elsevier BV]
卷期号:5: 15-23 被引量:89
标识
DOI:10.1016/j.redox.2015.02.004
摘要

Due to socioeconomic factors, more couples are choosing to delay conception than ever. Increasing average maternal and paternal age in developed countries over the past 40 years has raised the question of how aging affects reproductive success of males and females. Since oxidative stress in the male reproductive tract increases with age, we investigated the impact of advanced paternal age on the integrity of sperm nucleus and reproductive success of males by using a Prdx6(-/-) mouse model. We compared sperm motility, cytoplasmic droplet retention sperm chromatin quality and reproductive outcomes of young (2-month-old), adult (8-month-old), and old (20-month-old) Prdx6(-/-) males with their age-matched wild type (WT) controls. Absence of PRDX6 caused age-dependent impairment of sperm motility and sperm maturation and increased sperm DNA fragmentation and oxidation as well as decreased sperm DNA compaction and protamination. Litter size, total number of litters and total number of pups per male were significantly lower in Prdx6(-/-) males compared to WT controls. These abnormal reproductive outcomes were severely affected by age in Prdx6(-/-) males. In conclusion, the advanced paternal age affects sperm chromatin integrity and fertility more severely in the absence of PRDX6, suggesting a protective role of PRDX6 in age-associated decline in the sperm quality and fertility in mice.

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