Kageyama Haruaki, Kitamura Yoshitaka, Hosono Tomohiko, Kintaka Yuri, Seki Mayumi, Takenoya Fumiko, Hori Yasunori, Nonaka Naoko, Arata Satoru, Shioda Seiji
Department of Anatomy, Showa University School of Medicine, 1-5-8 Hatanodai Shinagawa-ku, Tokyo 142-8555, Japan.
Regul Pept. 2008 Jan 10;145(1-3):116-21. doi: 10.1016/j.regpep.2007.09.026. Epub 2007 Sep 25.
The gut-brain hormone ghrelin is known to stimulate growth hormone release from the pituitary gland, and to regulate appetite and energy metabolism. Ghrelin-containing neurons have been shown to form neuronal network with several types of appetite-regulating neurons in the hypothalamus. Although ghrelin-containing cell bodies have been reported to localize in the hypothalamic arcuate nucleus, the published results present large discrepancies regarding the localization of ghrelin-positive cell bodies in the brain. In order to address this issue, we have generated a transgenic mouse model by microinjecting a DNA construct in which the transcription regulatory regions of ghrelin drive the enhanced green fluorescent protein (EGFP) gene. These transgenic mice expressed EGFP and ghrelin mRNA in the stomach and hypothalamus. Double immunostaining revealed that GFP-like immunoreactivity was co-localized with ghrelin-like immunoreactivity in the stomach of these animals, while EGFP fluorescence was clearly demonstrated in the hypothalamic arcuate nucleus by confocal laser microscopy. The ghrelin-EGFP transgenic mouse model described in this study therefore provides a powerful tool with which to analyze ghrelin neuronal circuits in the brain and should contribute to our understanding of the functional significance of ghrelin in the central nervous system.
已知肠脑激素胃饥饿素可刺激垂体释放生长激素,并调节食欲和能量代谢。含胃饥饿素的神经元已被证明可与下丘脑多种类型的食欲调节神经元形成神经网络。尽管据报道含胃饥饿素的细胞体位于下丘脑弓状核,但已发表的结果在脑内胃饥饿素阳性细胞体的定位方面存在很大差异。为了解决这个问题,我们通过显微注射一种DNA构建体生成了一种转基因小鼠模型,其中胃饥饿素的转录调控区域驱动增强型绿色荧光蛋白(EGFP)基因。这些转基因小鼠在胃和下丘脑中表达EGFP和胃饥饿素mRNA。双重免疫染色显示,在这些动物的胃中,绿色荧光蛋白样免疫反应性与胃饥饿素样免疫反应性共定位,而通过共聚焦激光显微镜在下丘脑弓状核中清楚地显示了EGFP荧光。因此,本研究中描述的胃饥饿素-EGFP转基因小鼠模型提供了一个强大的工具,可用于分析脑中胃饥饿素神经元回路,并应有助于我们理解胃饥饿素在中枢神经系统中的功能意义。