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伏隔核D2神经元中Slc6a15的减少是应激易感性的基础。

Reduced Slc6a15 in Nucleus Accumbens D2-Neurons Underlies Stress Susceptibility.

作者信息

Chandra Ramesh, Francis T Chase, Nam Hyungwoo, Riggs Lace M, Engeln Michel, Rudzinskas Sarah, Konkalmatt Prasad, Russo Scott J, Turecki Gustavo, Iniguez Sergio D, Lobo Mary Kay

机构信息

Department of Anatomy and Neurobiology, University of Maryland School of Medicine, Baltimore, Maryland 21201.

Division of Renal Diseases and Hypertension, The George Washington University, Washington, DC 20037.

出版信息

J Neurosci. 2017 Jul 5;37(27):6527-6538. doi: 10.1523/JNEUROSCI.3250-16.2017. Epub 2017 Jun 2.

Abstract

Previous research demonstrates that Slc6a15, a neutral amino acid transporter, is associated with depression susceptibility. However, no study examined Slc6a15 in the ventral striatum [nucleus accumbens (NAc)] in depression. Given our previous characterization of Slc6a15 as a striatal dopamine receptor 2 (D2)-neuron-enriched gene, we examined the role of Slc6a15 in NAc D2-neurons in mediating susceptibility to stress in male mice. First, we showed that mRNA was reduced in NAc of mice susceptible to chronic social defeat stress (CSDS), a paradigm that produces behavioral and molecular adaptations that resemble clinical depression. Consistent with our preclinical data, we observed mRNA reduction in NAc of individuals with major depressive disorder (MDD). The Slc6a15 reduction in NAc occurred selectively in D2-neurons. Next, we used Cre-inducible viruses combined with D2-Cre mice to reduce or overexpress Slc6a15 in NAc D2-neurons. Slc6a15 reduction in D2-neurons caused enhanced susceptibility to a subthreshold social defeat stress (SSDS) as observed by reduced social interaction, while a reduction in social interaction following CSDS was not observed when Slc6a15 expression in D2-neurons was restored. Finally, since both D2-medium spiny neurons (MSNs) and D2-expressing choline acetyltransferase (ChAT) interneurons express Slc6a15, we examined Slc6a15 protein in these interneurons after CSDS. Slc6a15 protein was unaltered in ChAT interneurons. Consistent with this, reducing Slc5a15 selectively in NAc D2-MSNs, using A2A-Cre mice that express Cre selectively in D2-MSNs, caused enhanced susceptibility to SSDS. Collectively, our data demonstrate that reduced Slc6a15 in NAc occurs in MDD individuals and that Slc6a15 reduction in NAc D2-neurons underlies stress susceptibility. Our study demonstrates a role for reduced Slc6a15, a neutral amino acid transporter, in nucleus accumbens (NAc) in depression and stress susceptibility. The reduction of Slc6a15 occurs selectively in the NAc D2-neurons. Genetic reduction of Slc6a15 induces susceptibility to a subthreshold stress, while genetic overexpression in D2-neurons prevents social avoidance after chronic social defeat stress.

摘要

先前的研究表明,中性氨基酸转运体Slc6a15与抑郁症易感性相关。然而,尚无研究在抑郁症患者的腹侧纹状体[伏隔核(NAc)]中检测Slc6a15。鉴于我们之前将Slc6a15鉴定为富含纹状体多巴胺受体2(D2)神经元的基因,我们研究了Slc6a15在NAc D2神经元中介导雄性小鼠应激易感性的作用。首先,我们发现易患慢性社会挫败应激(CSDS)的小鼠NAc中mRNA减少,CSDS是一种产生类似于临床抑郁症的行为和分子适应性变化的范式。与我们的临床前数据一致,我们观察到重度抑郁症(MDD)患者NAc中mRNA减少。NAc中Slc6a15的减少选择性地发生在D2神经元中。接下来,我们使用Cre诱导型病毒结合D2-Cre小鼠来减少或过表达NAc D2神经元中的Slc6a15。D2神经元中Slc6a15的减少导致对阈下社会挫败应激(SSDS)的易感性增强,表现为社交互动减少,而当D2神经元中Slc6a15的表达恢复时,未观察到CSDS后社交互动的减少。最后,由于D2中型多棘神经元(MSNs)和表达D2的胆碱乙酰转移酶(ChAT)中间神经元均表达Slc6a15,我们在CSDS后检测了这些中间神经元中的Slc6a15蛋白。ChAT中间神经元中的Slc6a15蛋白未发生改变。与此一致的是,使用在D2-MSNs中选择性表达Cre的A2A-Cre小鼠在NAc D2-MSNs中选择性降低Slc5a15,导致对SSDS的易感性增强。总体而言,我们的数据表明,MDD个体中NAc中Slc6a15减少,且NAc D2神经元中Slc6a15减少是应激易感性的基础。我们的研究证明了中性氨基酸转运体Slc6a15减少在伏隔核(NAc)抑郁症和应激易感性中的作用。Slc6a15的减少选择性地发生在NAc D2神经元中。Slc6a15的基因敲低诱导对阈下应激的易感性,而在D2神经元中的基因过表达可防止慢性社会挫败应激后的社交回避。

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