Breaking the Chains: Advances in Substance Addiction Research through Single-Cell Sequencing, Epigenetics, and Epitranscriptomic

Ana Filošević Vujnović, Ivana Stanković Matić, Lara Saftić Martinović, Sanja Dević Pavlić
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Abstract

Addiction is a complex brain disease influenced by genetic, environmental, and neurological factors. Psychostimulants, cocaine, and methamphetamine influence different cell types in different brain regions, with a focus on the neurons responsible for rewarding effects in the nucleus accumbens (NAc) and ventral tegmental area (VTA). Known markers for psychostimulant-induced neuronal plasticity in combination with droplet-based high-throughput single-cell sequencing divided the heterogeneity of cell populations in NAc and VTA into clusters, where all cells of the same type do not respond equally to exposure to psychostimulants. To explain psychostimulant-induced neuronal plasticity as changes in the amplitude and phase shifts of gene expression, we focused on epigenetic mechanisms of DNA and chromatin modifications, as well as DNA accessibility. We also comment on epitranscriptomics as a novel approach in the study of messenger RNA posttranslational modification, which regulates translation and potentially localized transcription in synapses in order to address the molecular chains that connect addiction from changes in gene expression to synaptic and, finally, neuronal plasticity.
打破枷锁:通过单细胞测序、表观遗传学和表观转录组学推进药物成瘾研究
成瘾是一种复杂的脑部疾病,受遗传、环境和神经因素的影响。精神刺激剂、可卡因和甲基苯丙胺会影响不同脑区的不同细胞类型,重点是负责产生奖赏效应的神经元,它们位于伏隔核(NAc)和腹侧被盖区(VTA)。精神刺激剂诱导的神经元可塑性的已知标记物与基于液滴的高通量单细胞测序相结合,将NAc和VTA中细胞群的异质性划分为多个细胞簇,在这些细胞簇中,所有相同类型的细胞对暴露于精神刺激剂的反应并不相同。为了将精神刺激剂诱导的神经元可塑性解释为基因表达的幅度和相移变化,我们重点研究了DNA和染色质修饰的表观遗传机制以及DNA的可及性。我们还评论了表转录组学,将其作为研究信使 RNA 翻译后修饰的一种新方法,这种修饰可调控翻译和突触中潜在的局部转录,从而解决从基因表达变化到突触,最后到神经元可塑性的成瘾分子链问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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