精母细胞
磷脂过氧化氢谷胱甘肽过氧化物酶
GPX4
生物
男性不育
精子发生
男科
精子活力
精子
硒蛋白
线粒体
不育
内科学
内分泌学
谷胱甘肽过氧化物酶
细胞生物学
遗传学
超氧化物歧化酶
医学
氧化应激
减数分裂
基因
怀孕
作者
Hideki Imai,Nao Hakkaku,Ryo Iwamoto,Jun-Ichi Suzuki,Toshiyuki Suzuki,Yoko Tajima,Kumiko Konishi,Shintaro Minami,Shizuko Ichinose,Kazuhiro Ishizaka,Seiji Shioda,Satoru Arata,Masuhiro Nishimura,Shinsaku Naito,Yasuhito Nakagawa
标识
DOI:10.1074/jbc.m109.016139
摘要
Phospholipid hydroperoxide glutathione peroxidase (GPx4) is an intracellular antioxidant enzyme that directly reduces peroxidized phospholipids. GPx4 is strongly expressed in the mitochondria of testis and spermatozoa. We previously found a significant decrease in the expression of GPx4 in spermatozoa from 30% of infertile human males diagnosed with oligoasthenozoospermia (Imai, H., Suzuki, K., Ishizaka, K., Ichinose, S., Oshima, H., Okayasu, I., Emoto, K., Umeda, M., and Nakagawa, Y. (2001) Biol. Reprod. 64, 674-683). To clarify whether defective GPx4 in spermatocytes causes male infertility, we established spermatocyte-specific GPx4 knock-out mice using a Cre-loxP system. All the spermatocyte-specific GPx4 knock-out male mice were found to be infertile despite normal plug formation after mating and displayed a significant decrease in the number of spermatozoa. Isolated epididymal GPx4-null spermatozoa could not fertilize oocytes in vitro. These spermatozoa showed significant reductions of forward motility and the mitochondrial membrane potential. These impairments were accompanied by the structural abnormality, such as a hairpin-like flagella bend at the midpiece and swelling of mitochondria in the spermatozoa. These results demonstrate that the depletion of GPx4 in spermatocytes causes severe abnormalities in spermatozoa. This may be one of the causes of male infertility in mice and humans.
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