Aberrant encoding of event saliency in the orbitofrontal cortex following loss of the psychiatric-associated circular RNA, circHomer1.

IF 5.8 1区 医学 Q1 PSYCHIATRY
Amber J Zimmerman, Jason P Weick, Grigorios Papageorgiou, Nikolaos Mellios, Jonathan L Brigman
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引用次数: 0

Abstract

CircHomer1 is an activity-dependent circular RNA (circRNA) isoform produced from back-splicing of the Homer1 transcript. Homer1 isoforms are well-known regulators of homeostatic synaptic plasticity through post-synaptic density scaffold regulation. Homer1 polymorphisms have been associated with psychiatric diseases including schizophrenia (SCZ) and bipolar disorder (BD). Postmortem tissue from patients with SCZ and BD displayed reduced circHomer1 levels within the orbitofrontal cortex (OFC), a region that tracks event saliency important for modulating behavioral flexibility. While dysregulation of circHomer1 expression has recently been identified across multiple psychiatric and neurodegenerative disorders and is associated with impaired behavioral flexibility in mice, it is unknown whether circHomer1 can induce electrophysiological signatures relevant to cognitive dysfunction in these disorders. To examine the role of circHomer1 in neuronal signaling, we bilaterally knocked down circHomer1 in the OFC of C57BL/6 J male mice and recorded neural activity from the OFC during a touchscreen reversal learning task then measured molecular changes of synaptic regulators following knockdown. Knockdown of circHomer1 within the OFC induced choice-dependent changes in multiunit firing rate and local field potential coordination and power to salient stimuli during reversal learning. Further, these electrophysiological changes were associated with transcriptional downregulation of glutamatergic signaling effectors and behavioral alterations leading to impaired cognitive flexibility. CircHomer1 is a stable biomolecule, whose knockdown in rodent OFC produces lasting electrophysiological and transcriptional changes important for efficient reversal learning. This is, to our knowledge, the first demonstration of a psychiatric-associated circRNA contributing to electrophysiological, transcriptional, and behavioral alterations relevant to psychiatric phenotypes.

精神病相关环状RNA circHomer1缺失后,眶额叶皮层事件显著性编码异常。
CircHomer1是一种活性依赖性环状RNA (circRNA)异构体,由Homer1转录物的反向剪接产生。Homer1同种异构体是众所周知的通过突触后密度支架调节突触稳态可塑性的调节剂。Homer1多态性与精神分裂症(SCZ)和双相情感障碍(BD)等精神疾病有关。SCZ和BD患者的死后组织显示眶额皮质(OFC)中的circHomer1水平降低,OFC是一个跟踪事件显著性的区域,对调节行为灵活性很重要。虽然circHomer1表达失调最近在多种精神和神经退行性疾病中被发现,并与小鼠行为灵活性受损有关,但circHomer1是否能诱导与这些疾病中认知功能障碍相关的电生理特征尚不清楚。为了研究circHomer1在神经元信号传导中的作用,我们在C57BL/6 J雄性小鼠的OFC中双侧敲除circHomer1,并在触屏反向学习任务中记录OFC的神经活动,然后测量敲除后突触调节因子的分子变化。在反向学习过程中,OFC内circHomer1的敲除诱导了多单元放电速率、局部场电位协调和对显著刺激的能力的选择依赖性变化。此外,这些电生理变化与谷氨酸信号效应的转录下调和导致认知灵活性受损的行为改变有关。CircHomer1是一种稳定的生物分子,其在啮齿动物OFC中的敲除会产生持久的电生理和转录变化,这对有效的逆转学习至关重要。据我们所知,这是首次证明精神病相关的circRNA有助于与精神病表型相关的电生理、转录和行为改变。
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来源期刊
CiteScore
11.50
自引率
2.90%
发文量
484
审稿时长
23 weeks
期刊介绍: Psychiatry has suffered tremendously by the limited translational pipeline. Nobel laureate Julius Axelrod''s discovery in 1961 of monoamine reuptake by pre-synaptic neurons still forms the basis of contemporary antidepressant treatment. There is a grievous gap between the explosion of knowledge in neuroscience and conceptually novel treatments for our patients. Translational Psychiatry bridges this gap by fostering and highlighting the pathway from discovery to clinical applications, healthcare and global health. We view translation broadly as the full spectrum of work that marks the pathway from discovery to global health, inclusive. The steps of translation that are within the scope of Translational Psychiatry include (i) fundamental discovery, (ii) bench to bedside, (iii) bedside to clinical applications (clinical trials), (iv) translation to policy and health care guidelines, (v) assessment of health policy and usage, and (vi) global health. All areas of medical research, including — but not restricted to — molecular biology, genetics, pharmacology, imaging and epidemiology are welcome as they contribute to enhance the field of translational psychiatry.
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