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利用新生成的Kiss1基因条件性敲除小鼠和Kiss1-Cre小鼠进行的条件性促性腺激素释放激素神经元特异性Kiss1基因敲除,重现了全身性Kiss1基因敲除小鼠的性腺功能减退表型。

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

作者信息

Ikegami Kana, Goto Teppei, Nakamura Sho, Watanabe Youki, Sugimoto Arisa, Majarune Sutisa, Horihata Kei, Nagae Mayuko, Tomikawa Junko, Imamura Takuya, Sanbo Makoto, Hirabayashi Masumi, Inoue Naoko, Maeda Kei-Ichiro, Tsukamura Hiroko, Uenoyama Yoshihisa

机构信息

Graduate School of Bioagricultural Sciences, Nagoya University, Nagoya 464-8601, Japan.

Center for Genetic Analysis of Behavior, National Institute for Physiological Sciences, Okazaki 444-8585, Japan.

出版信息

J Reprod Dev. 2020 Aug 20;66(4):359-367. doi: 10.1262/jrd.2020-026. Epub 2020 Apr 20.

Abstract

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.

摘要

本研究旨在评估利用Cre-loxP系统构建的新型条件性促性腺激素释放激素神经元特异性Kiss1基因敲除(KO)小鼠是否能够重现全身性Kiss1基因敲除模型的不育现象,从而为下丘脑促性腺激素释放激素神经元在调节哺乳动物生殖中的基本作用提供进一步证据。我们构建了Kiss1基因条件性敲除小鼠和下丘脑促性腺激素释放激素神经元特异性表达Cre的转基因小鼠,然后将这两个品系进行杂交。条件性Kiss1基因敲除小鼠出现青春期发育失败,同时伴有促性腺激素分泌受抑制和卵巢萎缩。这些结果表明,通过Cre-loxP系统获得的新构建的下丘脑Kiss1基因敲除小鼠重现了全身性Kiss1基因敲除模型的不育现象,提示下丘脑促性腺激素释放激素而非外周促性腺激素释放激素对生殖至关重要。重要的是,这些Kiss1基因条件性敲除小鼠现已可用,将成为通过时空特异性操纵Cre表达来详细分析大脑中各群促性腺激素释放激素神经元和外周促性腺激素释放激素产生细胞作用的宝贵工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42c1/7470906/f483ae86a7b5/jrd-66-359-g001.jpg

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