Schell Grant, Roy Bhaskar, Prall Kevin, Dwivedi Yogesh
Department of Psychiatry and Behavioral Neurobiology, Heersink School of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Noncoding RNA. 2022 Jul 21;8(4):55. doi: 10.3390/ncrna8040055.
Understanding the epigenetic role of microRNAs (miRNAs) has been a critical development in the field of neuropsychiatry and in understanding their underlying pathophysiology. Abnormalities in miRNA expression are often seen as key to the pathogenesis of many stress-associated mental disorders, including major depressive disorder (MDD). Recent advances in omics biology have further contributed to this understanding and expanded the role of miRNAs in networking a diverse array of molecular pathways, which are essentially related to the stress adaptivity of a healthy brain. Studies have highlighted the role of many such miRNAs in causing maladaptive changes in the brain's stress axis. One such miRNA is miR-218, which is debated as a critical candidate for increased stress susceptibility. miR-218 is expressed throughout the brain, notably in the hippocampus and prefrontal cortex (PFC). It is expressed at various levels through life stages, as seen by adolescent and adult animal models. Until now, a minimal number of studies have been conducted on human subjects to understand its role in stress-related abnormalities in brain circuits. However, several studies, including animal and cell-culture models, have been used to understand the impact of miR-218 on stress response and hypothalamic-pituitary-adrenal (HPA) axis function. So far, expression changes in this miRNA have been found to regulate signaling pathways such as glucocorticoid signaling, serotonergic signaling, and glutamatergic signaling. Recently, the developmental role of miR-218 has generated interest, given its increasing expression from adolescence to adulthood and targeting the Netrin-1/DCC signaling pathway. Since miR-218 expression affects neuronal development and plasticity, it is expected that a change in miR-218 expression levels over the course of development may negatively impact the process and make individuals stress-susceptible in adulthood. In this review, we describe the role of miR-218 in stress-induced neuropsychiatric conditions with an emphasis on stress-related disorders.
了解微小RNA(miRNA)的表观遗传作用,是神经精神病学领域以及理解其潜在病理生理学的一项关键进展。miRNA表达异常通常被视为包括重度抑郁症(MDD)在内的许多与应激相关的精神障碍发病机制的关键因素。组学生物学的最新进展进一步推动了这一认识,并扩展了miRNA在连接各种分子途径网络中的作用,这些途径本质上与健康大脑的应激适应性相关。研究突出了许多此类miRNA在导致大脑应激轴出现适应不良变化方面的作用。其中一种miRNA是miR-218,它被认为是应激易感性增加的关键候选分子。miR-218在整个大脑中表达,尤其在海马体和前额叶皮质(PFC)中。从青春期和成年动物模型可以看出,它在生命的各个阶段都有不同水平的表达。到目前为止,针对人类受试者开展的旨在了解其在脑回路应激相关异常中作用的研究数量极少。然而,包括动物和细胞培养模型在内的多项研究已被用于了解miR-218对应激反应和下丘脑-垂体-肾上腺(HPA)轴功能的影响。迄今为止,已发现这种miRNA的表达变化可调节糖皮质激素信号传导、血清素能信号传导和谷氨酸能信号传导等信号通路。最近,鉴于miR-218从青春期到成年期表达增加并靶向Netrin-1/DCC信号通路,其在发育过程中的作用引起了人们的兴趣。由于miR-218的表达会影响神经元发育和可塑性,因此预计在发育过程中miR-218表达水平的变化可能会对这一过程产生负面影响,并使个体在成年后易受应激影响。在这篇综述中,我们描述了miR-218在应激诱导的神经精神疾病中的作用,重点关注与应激相关的疾病。