GPX4
脂质过氧化
生物
程序性细胞死亡
机制(生物学)
精子发生
生殖系统
疾病
内生
细胞生物学
细胞凋亡
遗传学
氧化应激
医学
内科学
内分泌学
哲学
过氧化氢酶
认识论
谷胱甘肽过氧化物酶
作者
Wenzheng Yuan,Zhibin Sun,Guojie Ji,Huanhuan Hu
标识
DOI:10.1038/s41420-023-01665-x
摘要
Ferroptosis is a type of programmed cell death mediated by iron-dependent lipid peroxidation that leads to excessive lipid peroxidation in different cells. Ferroptosis is distinct from other forms of cell death and is associated with various diseases. Iron is essential for spermatogenesis and male reproductive function. Therefore, it is not surprising that new evidence supports the role of ferroptosis in testicular injury. Although the molecular mechanism by which ferroptosis induces disease is unknown, several genes and pathways associated with ferroptosis have been linked to testicular dysfunction. In this review, we discuss iron metabolism, ferroptosis, and related regulatory pathways. In addition, we analyze the endogenous and exogenous factors of ferroptosis in terms of iron metabolism and testicular dysfunction, as well as summarize the relationship between ferroptosis and male reproductive dysfunction. Finally, we discuss potential strategies to target ferroptosis for treating male reproductive diseases and provide new directions for preventing male reproductive diseases.
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