Cleverdon Elizabeth R, McGovern-Gooch Kayleigh R, Hougland James L
a Department of Chemistry , Syracuse University , Syracuse , NY , USA.
Mol Membr Biol. 2016 Sep-Dec;33(6-8):111-124. doi: 10.1080/09687688.2017.1388930. Epub 2017 Nov 16.
Ghrelin is a small peptide hormone that requires a unique post-translational modification, serine octanoylation, to bind and activate the GHS-R1a receptor. Initially demonstrated to stimulate hunger and appetite, ghrelin-dependent signaling is implicated in a variety of neurological and physiological processes influencing diseases such as diabetes, obesity, and Prader-Willi syndrome. In addition to its cognate receptor, recent studies have revealed ghrelin interacts with a range of binding partners within the bloodstream. Defining the scope of ghrelin's interactions within the body, understanding how these interactions work in concert to modulate ghrelin signaling, and developing molecular tools for controlling ghrelin signaling are essential for exploiting ghrelin for therapeutic effect. In this review, we discuss recent findings regarding the biological effects of ghrelin signaling, outline binding partners that control ghrelin trafficking and stability in circulation, and summarize the current landscape of inhibitors targeting ghrelin octanoylation.
胃饥饿素是一种小肽激素,需要独特的翻译后修饰——丝氨酸辛酰化,才能结合并激活生长激素促分泌素受体1a(GHS-R1a)。胃饥饿素最初被证明能刺激饥饿和食欲,其依赖的信号传导参与了多种影响糖尿病、肥胖症和普拉德-威利综合征等疾病的神经和生理过程。除了其同源受体外,最近的研究还表明胃饥饿素与血液中的一系列结合伙伴相互作用。明确胃饥饿素在体内的相互作用范围,了解这些相互作用如何协同调节胃饥饿素信号传导,以及开发控制胃饥饿素信号传导的分子工具,对于利用胃饥饿素实现治疗效果至关重要。在这篇综述中,我们讨论了关于胃饥饿素信号传导生物学效应的最新发现,概述了控制胃饥饿素在循环中运输和稳定性的结合伙伴,并总结了目前针对胃饥饿素辛酰化的抑制剂情况。