Department of Biochemistry and Molecular Biology, New York Medical College, Valhalla, NY 10595, United States.
Nash Family Department of Neuroscience and Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, United States.
Behav Brain Res. 2023 Feb 15;439:114162. doi: 10.1016/j.bbr.2022.114162. Epub 2022 Oct 17.
Although most people are subjected to traumatic stress at least once in their lifetime, only a subset develop long-lasting, stress-triggered neuropsychiatric disorders, such as PTSD. Here we examined different transcriptome profiles within the locus coeruleus (LC) and nucleus accumbens (NAc) that may contribute to stress susceptibility. Sprague Dawley male rats were exposed to the single prolonged stress (SPS) model for PTSD. Two weeks later they were tested for their anxiety/avoidance behavior on the Elevated Plus Maze (EPM) and were divided into high and low anxiety-like subgroups. RNA (n = 5 per group) was subsequently isolated from LC and NAc and subjected to RNAseq. Transcriptome analysis was used to identify differentially-expressed genes (DEGs) which differed by at least 50 % with significance of 0.01. The LC had more than six times the number of DEGs than the NAc. Only one DEG was regulated similarly in both locations. Many of the DEGs in the LC were associated with morphological changes, including regulation of actin cytoskeleton, growth factor activity, regulation of cell size, brain development and memory, with KEGG pathway of regulation of actin cytoskeleton. The DEGs in the NAc were primarily related to DNA repair and synthesis, and differential regulation of cytokine production. The analysis identified MTPN (myotrophin) and NR3C1 (glucocorticoid receptor) as important upstream regulators of stress susceptibility in the LC. Overall the study provides new insight into molecular pathways in the LC and NAc that are associated with anxiety-like behavior triggered by stress susceptibility or resilience.
尽管大多数人一生中至少会经历一次创伤性应激,但只有一部分人会发展出持久的、应激触发的神经精神障碍,如 PTSD。在这里,我们研究了蓝斑核(LC)和伏隔核(NAc)内可能导致应激易感性的不同转录组谱。雄性 Sprague Dawley 大鼠接受创伤后应激障碍的单次延长应激(SPS)模型。两周后,他们在高架十字迷宫(EPM)上测试其焦虑/回避行为,并分为高和低焦虑样亚组。随后从 LC 和 NAc 中分离 RNA(每组 n=5)并进行 RNAseq。转录组分析用于鉴定差异表达基因(DEG),其差异至少为 50%,显著性为 0.01。LC 的 DEG 数量是 NAc 的六倍多。只有一个 DEG 在两个位置的调节方式相似。LC 中的许多 DEG 与形态变化有关,包括肌动蛋白细胞骨架的调节、生长因子活性、细胞大小的调节、脑发育和记忆,KEGG 途径为肌动蛋白细胞骨架的调节。NAc 中的 DEG 主要与 DNA 修复和合成以及细胞因子产生的差异调节有关。该分析确定了 MTPN(肌萎缩蛋白)和 NR3C1(糖皮质激素受体)作为 LC 中应激易感性的重要上游调节因子。总的来说,该研究为 LC 和 NAc 中与应激易感性或弹性引发的焦虑样行为相关的分子途径提供了新的见解。