Medical Research Council Human Reproductive Sciences Unit, The Queen's Medical Research Institute, 47 Little France Crescent, Edinburgh EH16 4TJ, Scotland, UK.
J Mol Endocrinol. 2010 Apr;44(4):195-201. doi: 10.1677/JME-09-0168. Epub 2010 Feb 4.
The binding of GnRH to its receptor on pituitary gonadotropes leads to the targeting of a diverse array of signalling mediators. These mediators drive multiple signal transduction pathways, which in turn regulate a variety of cellular processes, including the biosynthesis and secretion of the gonadotropins LH and FSH. Advances in our understanding of the mechanisms and signalling pathways that are recruited to regulate gonadotrope function are continually being made. This review will focus on the recent demonstration that key mediators of the canonical Wnt signalling pathway are targeted by GnRH in gonadotropes, and that these may play essential roles in regulating the expression of many of the key players in gonadotrope biology, including the GnRH receptor and the gonadotropins.
GnRH 与其在垂体促性腺激素细胞上的受体结合,导致靶向多种信号转导介质。这些介质驱动多种信号转导途径,进而调节多种细胞过程,包括促性腺激素 LH 和 FSH 的生物合成和分泌。我们对招募来调节促性腺激素细胞功能的机制和信号转导途径的理解不断取得进展。本综述将重点介绍最近的研究结果,即 GnRH 在促性腺激素细胞中靶向经典 Wnt 信号通路的关键介质,并且这些介质可能在调节许多促性腺激素生物学中的关键参与者的表达中发挥重要作用,包括 GnRH 受体和促性腺激素。