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促性腺激素抑制激素(GnIH)在靶细胞中的作用分子机制及GnIH表达的调控

Molecular Mechanisms of Gonadotropin-Inhibitory Hormone (GnIH) Actions in Target Cells and Regulation of GnIH Expression.

作者信息

Son You Lee, Ubuka Takayoshi, Tsutsui Kazuyoshi

机构信息

Laboratory of Photobiology, Department of Ophthalmology, Keio University School of Medicine, Tokyo, Japan.

Laboratory of Integrative Brain Sciences, Department of Biology and Center for Medical Life Science, Waseda University, Tokyo, Japan.

出版信息

Front Endocrinol (Lausanne). 2019 Feb 25;10:110. doi: 10.3389/fendo.2019.00110. eCollection 2019.

Abstract

Since gonadotropin-inhibitory hormone (GnIH) was discovered in 2000 as the first hypothalamic neuropeptide that actively inhibits gonadotropin release, researches conducted for the last 18 years have demonstrated that GnIH acts as a pronounced negative regulator of reproduction. Inhibitory effect of GnIH on reproduction is mainly accomplished at hypothalamic-pituitary levels; gonadotropin-releasing hormone (GnRH) neurons and gonadotropes are major targets of GnIH action based on the morphological interaction with GnIH neuronal fibers and the distribution of GnIH receptor. Here, we review molecular studies mainly focusing on the signal transduction pathway of GnIH in target cells, GnRH neurons, and gonadotropes. The use of well-defined cellular model systems allows the mechanistic study of signaling pathway occurring in target cells by demonstrating the direct cause-and-effect relationship. The insights gained through studying molecular mechanism of GnIH action contribute to deeper understanding of the mechanism of how GnIH communicates with other neuronal signaling systems to control our reproductive function. Reproductive axis closely interacts with other endocrine systems, thus GnIH expression levels would be changed by adrenal and thyroid status. We also briefly review molecular studies investigating the regulatory mechanisms of GnIH expression to understand the role of GnIH as a mediator between adrenal, thyroid and gonadal axes.

摘要

自2000年促性腺激素抑制激素(GnIH)作为首个能主动抑制促性腺激素释放的下丘脑神经肽被发现以来,过去18年的研究表明,GnIH是一种显著的生殖负调节因子。GnIH对生殖的抑制作用主要在下丘脑 - 垂体水平实现;基于与GnIH神经元纤维的形态学相互作用以及GnIH受体的分布,促性腺激素释放激素(GnRH)神经元和促性腺激素细胞是GnIH作用的主要靶点。在此,我们综述主要聚焦于GnIH在靶细胞、GnRH神经元和促性腺激素细胞中信号转导途径的分子研究。使用定义明确的细胞模型系统,通过证明直接的因果关系,能够对靶细胞中发生的信号通路进行机制研究。通过研究GnIH作用的分子机制所获得的见解,有助于更深入地理解GnIH如何与其他神经元信号系统相互作用以控制我们生殖功能的机制。生殖轴与其他内分泌系统密切相互作用,因此GnIH的表达水平会因肾上腺和甲状腺状态而改变。我们还简要综述了研究GnIH表达调控机制的分子研究,以了解GnIH作为肾上腺、甲状腺和性腺轴之间介质的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/baf8/6397841/444f700bc2be/fendo-10-00110-g0001.jpg

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