卵母细胞
氧化应激
活性氧
生物
线粒体
细胞生物学
线粒体DNA
端粒
DNA损伤
线粒体ROS
男科
自噬
非整倍体
内科学
内分泌学
遗传学
细胞凋亡
医学
DNA
胚胎
染色体
基因
作者
Hiroyuki Sasaki,Toshio Hamatani,Shintaro Kamijo,Maki Iwai,Masato Kobanawa,Seiji Ogawa,Kenji Miyado,Mamoru Tanaka
标识
DOI:10.3389/fendo.2019.00811
摘要
Reproductive capacity in women starts to decline beyond their mid-30s and pregnancies in older women result in higher rates of miscarriage with aneuploidy. Age-related decline in fertility is strongly attributed to ovarian aging, diminished ovarian reserves, and decreased developmental competence of oocytes. In this review, we discuss the underlying mechanisms of age-related decline in oocyte quality, focusing on oxidative stress (OS) in oocytes. The primary cause is the accumulation of spontaneous damage to the mitochondria arising from increased reactive oxygen species (ROS) in oocytes, generated by the mitochondria themselves during daily biological metabolism. Mitochondrial dysfunction reduces ATP synthesis and influences the meiotic spindle assembly responsible for chromosomal segregation. Moreover, reproductively aged oocytes produce a decline in the fidelity of the protective mechanisms against ROS, namely the ROS-scavenging metabolism, repair of ROS-damaged DNA, and the proteasome and autophagy system for ROS-damaged proteins. Accordingly, increased ROS and increased vulnerability of oocytes to ROS lead to spindle instability, chromosomal abnormalities, telomere shortening, and reduced developmental competence of aged oocytes.
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