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微小RNA let-7d是大麻素CB1受体的一个靶点,并调控大麻素信号传导。

MicroRNA let-7d is a target of cannabinoid CB1 receptor and controls cannabinoid signaling.

作者信息

Chiarlone Anna, Börner Christine, Martín-Gómez Laura, Jiménez-González Ada, García-Concejo Adrián, García-Bermejo María L, Lorente Mar, Blázquez Cristina, García-Taboada Elena, de Haro Amador, Martella Elisa, Höllt Volker, Rodríguez Raquel, Galve-Roperh Ismael, Kraus Jürgen, Guzmán Manuel

机构信息

Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED) and Instituto Universitario de Investigación Neuroquímica (IUIN), Department of Biochemistry and Molecular Biology I, Complutense University, 28040 Madrid, Spain; Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS), 28034 Madrid, Spain.

Department of Pharmacology and Toxicology, University of Magdeburg, 39106 Magdeburg, Germany.

出版信息

Neuropharmacology. 2016 Sep;108:345-52. doi: 10.1016/j.neuropharm.2016.05.007. Epub 2016 May 11.

Abstract

Cannabinoid CB1 receptor, the molecular target of endocannabinoids and cannabis active components, is one of the most abundant metabotropic receptors in the brain. Cannabis is widely used for both recreational and medicinal purposes. Despite the ever-growing fundamental roles of microRNAs in the brain, the possible molecular connections between the CB1 receptor and microRNAs are surprisingly unknown. Here, by using reporter gene constructs that express interaction sequences for microRNAs in human SH-SY5Y neuroblastoma cells, we show that CB1 receptor activation enhances the expression of several microRNAs, including let-7d. This was confirmed by measuring hsa-let-7d expression levels. Accordingly, knocking-down CB1 receptor in zebrafish reduced dre-let-7d levels, and knocking-out CB1 receptor in mice decreased mmu-let-7d levels in the cortex, striatum and hippocampus. Conversely, knocking-down let-7d increased CB1 receptor mRNA expression in zebrafish, SH-SY5Y cells and primary striatal neurons. Likewise, in primary striatal neurons chronically exposed to a cannabinoid or opioid agonist, a let-7d-inhibiting sequence facilitated not only cannabinoid or opioid signaling but also cannabinoid/opioid cross-signaling. Taken together, these findings provide the first evidence for a bidirectional link between the CB1 receptor and a microRNA, namely let-7d, and thus unveil a new player in the complex process of cannabinoid action.

摘要

大麻素CB1受体是内源性大麻素和大麻活性成分的分子靶点,是大脑中最丰富的代谢型受体之一。大麻被广泛用于娱乐和医疗目的。尽管微小RNA在大脑中的基础作用不断增加,但CB1受体与微小RNA之间可能的分子联系却惊人地未知。在这里,通过在人SH-SY5Y神经母细胞瘤细胞中使用表达微小RNA相互作用序列的报告基因构建体,我们表明CB1受体激活增强了包括let-7d在内的几种微小RNA的表达。通过测量hsa-let-7d表达水平证实了这一点。相应地,敲低斑马鱼中的CB1受体会降低dre-let-7d水平,敲除小鼠中的CB1受体会降低皮质、纹状体和海马体中的mmu-let-7d水平。相反,敲低let-7d会增加斑马鱼、SH-SY5Y细胞和原代纹状体神经元中CB1受体mRNA的表达。同样,在长期暴露于大麻素或阿片类激动剂的原代纹状体神经元中,let-7d抑制序列不仅促进了大麻素或阿片类信号传导,还促进了大麻素/阿片类交叉信号传导。综上所述,这些发现首次证明了CB1受体与微小RNA(即let-7d)之间存在双向联系,从而揭示了大麻素作用复杂过程中的一个新因素。

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