Conditional kisspeptin neuron-specific Kiss1 knockout with newly generated Kiss1-floxed and Kiss1-Cre mice replicates a hypogonadal phenotype of global Kissl knockout mice

被引:0
作者
Ikegami, Kana [1 ]
Goto, Teppei [1 ,2 ]
Nakamura, Sho [3 ]
Watanabe, Youki [1 ]
Sugimoto, Arisa [1 ]
Majarune, Sutisa [1 ]
Horihata, Kei [1 ]
Nagae, Mayuko [1 ]
Tomikawa, Junko [1 ]
Imamura, Takuya [4 ]
Sanbo, Makoto [2 ]
Hirabayashi, Masumi [2 ]
Inoue, Naoko [1 ]
Maeda, Kei-ichiro [3 ]
Tsukamura, Hiroko [1 ]
Uenoyama, Yoshihisa [1 ]
机构
[1] Nagoya Univ, Grad Sch Bioagr Sci, Nagoya, Aichi 4648601, Japan
[2] Natl Inst Physiol Sci, Ctr Genet Anal Behav, Okazaki, Aichi 4448585, Japan
[3] Univ Tokyo, Grad Sch Agr & Life Sci, Tokyo 1138657, Japan
[4] Hiroshima Univ, Grad Sch Integrated Sci Life, Hiroshima 7398526, Japan
基金
日本学术振兴会;
关键词
Cre/loxP system; Gonadotropin; Kisspeptin; Pubertal failure; GONADOTROPIN-RELEASING-HORMONE; POSITIVE FEEDBACK ACTION; GNRH PULSE-GENERATOR; SEXUAL-DIFFERENTIATION; ARCUATE NUCLEUS; NEUROKININ B; PUBERTAL INCREASE; GENE-EXPRESSION; SECRETION; PULSATILE;
D O I
暂无
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
The present study aimed to evaluate whether novel conditional kisspeptin neuron-specific Kiss1 knockout (KO) mice utilizing the Cre-loxP system could recapitulate the infertility of global Kiss1 KO models, thereby providing further evidence for the fundamental role of hypothalamic kisspeptin neurons in regulating mammalian reproduction. We generated Kiss1-floxed mice and hypothalamic kisspeptin neuron-specific Cre-expressing transgenic mice and then crossed these two lines. The conditional Kiss1 KO mice showed pubertal failure along with a suppression of gonadotropin secretion and ovarian atrophy. These results indicate that newly-created hypothalamic Kiss1 KO mice obtained by the Cre-loxP system recapitulated the infertility of global Kiss1 KO models, suggesting that hypothalamic kisspeptin, but not peripheral kisspeptin, is critical for reproduction. Importantly, these Kiss1-floxed mice are now available and will be a valuable tool for detailed analyses of roles of each population of kisspeptin neurons in the brain and peripheral kisspeptin-producing cells by the spatiotemporal-specific manipulation of Cre expression.
引用
收藏
页码:359 / 367
页数:9
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