Depletion of Selenoprotein GPx4 in Spermatocytes Causes Male Infertility in Mice

被引:169
作者
Imai, Hirotaka [1 ,2 ]
Hakkaku, Nao
Iwamoto, Ryo
Suzuki, Jyunko
Suzuki, Toshiyuki
Tajima, Yoko
Konishi, Kumiko
Minami, Shintaro [1 ]
Ichinose, Shizuko [3 ]
Ishizaka, Kazuhiro [4 ]
Shioda, Seiji [5 ]
Arata, Satoru [6 ]
Nishimura, Masuhiro [7 ]
Naito, Shinsaku [7 ]
Nakagawa, Yasuhito
机构
[1] Kitasato Univ, Sch Pharmaceut Sci, Minato Ku, Tokyo 1088641, Japan
[2] Japan Sci & Technol Agcy, PRESTO, Kawaguchi, Saitama 3320012, Japan
[3] Tokyo Med & Dent Univ, Sch Med, Instrumental Anal Res Ctr, Bunkyo Ku, Tokyo 1138510, Japan
[4] Kanto Cent Hosp, Mutual Aid Assoc, Publ Sch Teachers, Dept Urol,Setagaya Ku, Tokyo 1588531, Japan
[5] Showa Univ, Ctr Biotechnol, Shinagawa Ku, Tokyo 1428555, Japan
[6] Showa Univ, Dept Anat, Shinagawa Ku, Sch Med, Tokyo 1428555, Japan
[7] Otsuka Amer Pharmaceut Inc, Div Pharmacol Drug Safety & Metab, Tokushima 7728601, Japan
基金
日本科学技术振兴机构;
关键词
HYDROPEROXIDE GLUTATHIONE-PEROXIDASE; SPERM DEVELOPMENT; MAMMALIAN-CELLS; BINDING-PROTEIN; PHGPX GENE; EXPRESSION; IDENTIFICATION; FERTILITY; TRANSCRIPTION; MITOCHONDRIA;
D O I
10.1074/jbc.M109.016139
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
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 CreloxP 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.
引用
收藏
页码:32522 / 32532
页数:11
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