ACS Chem Neurosci. 2015 Jul 15;6(7):951-60. doi: 10.1021/cn500326z. Epub 2015 Jan 28.
5-HT6 receptor (5-HT6R) is a G protein-coupled receptor that has recently emerged as a new regulator of neural development. In addition to the canonical Gs adenylyl cyclase pathway, recent proteomics approaches reveal that 5-HT6R is able to engage key developmental signaling pathways controlling neuronal circuit formation, neuronal connectivity, and psychiatric-relevant behaviors. For example, at early stages of neuronal development, expression of 5-HT6R constitutively regulates the activity of the cyclin-dependent kinase (Cdk)5 and, through this mechanism, controls cellular processes involved in circuit formation, including neuronal migration and neurite outgrowth. In addition to the Cdk5 pathway, 5-HT6R modulates a variety of key developmental targets such as Fyn, Jab1, and mammalian target of rapamycin (mTOR). Engagement of developmental pathways through 5-HT6R pharmacological manipulation has led to interesting new therapeutic perspectives in the field of psychiatric-related disorders. Indeed, 5-HT6R blockade can rescue a pathological overactivation of the mTOR pathway induced by early life insults in rodents and normalizes the associated social and episodic memory deficits. Here, we review recent evidence supporting the notion that 5-HT6R is at the interface of key developmental signaling pathways and a novel actor in the orchestration of neural circuit formation.
5-羟色胺 6 受体(5-HT6R)是一种 G 蛋白偶联受体,最近被认为是神经发育的新调节因子。除了经典的 Gs 腺苷酸环化酶途径外,最近的蛋白质组学方法表明,5-HT6R 能够参与控制神经元回路形成、神经元连接和与精神疾病相关行为的关键发育信号通路。例如,在神经元发育的早期阶段,5-HT6R 的表达持续调节周期蛋白依赖性激酶(Cdk)5 的活性,通过这种机制,控制与回路形成相关的细胞过程,包括神经元迁移和轴突生长。除了 Cdk5 途径外,5-HT6R 还调节多种关键发育靶标,如 Fyn、Jab1 和雷帕霉素靶蛋白(mTOR)。通过 5-HT6R 药理学干预激活发育途径,为精神疾病相关障碍领域带来了有趣的新治疗前景。事实上,5-HT6R 阻断可以挽救早期生活创伤诱导的啮齿动物中 mTOR 途径的病理性过度激活,并使相关的社交和情景记忆缺陷正常化。在这里,我们回顾了最近的证据,支持 5-HT6R 处于关键发育信号通路的界面以及神经回路形成的新型调节因子的观点。