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肌张力障碍小鼠模型中纹状体突触异常成熟和分泌途径改变的遗传学证据。

Genetic evidence of aberrant striatal synaptic maturation and secretory pathway alteration in a dystonia mouse model.

作者信息

Yellajoshyula Dhananjay, Opeyemi Sunday, Dauer William T, Pappas Samuel S

机构信息

Department of Neurosciences, Case Western Reserve University, Cleveland, OH, United States.

Peter O'Donnell Jr. Brain Institute, University of Texas Southwestern Medical Center, Dallas, TX, United States.

出版信息

Dystonia. 2022;1. doi: 10.3389/dyst.2022.10892. Epub 2022 Dec 14.

Abstract

Animal models of DYT-TOR1A dystonia consistently demonstrate abnormalities of striatal cholinergic function, but the molecular pathways underlying this pathophysiology are unclear. To probe these molecular pathways in a genetic model of DYT-TOR1A, we performed laser microdissection in juvenile mice to isolate striatal cholinergic interneurons and non-cholinergic striatal tissue largely comprising spiny projection neurons during maturation. Both cholinergic and GABAergic enriched samples demonstrated a defined set of gene expression changes consistent with a role of torsinA in the secretory pathway. GABAergic enriched striatum samples also showed alteration to genes regulating synaptic transmission and an upregulation of activity dependent immediate early genes. Reconstruction of Golgi-Cox stained striatal spiny projection neurons from adult mice demonstrated significantly increased spiny density, suggesting that torsinA null striatal neurons have increased excitability during striatal maturation and long lasting increases in afferent input. These findings are consistent with a developmental role for torsinA in the secretory pathway and link torsinA loss of function with functional and structural changes of striatal cholinergic and GABAergic neurons. These transcriptomic datasets are freely available as a resource for future studies of torsinA loss of function-mediated striatal dysfunction.

摘要

DYT - TOR1A肌张力障碍的动物模型始终显示出纹状体胆碱能功能异常,但其病理生理学的分子途径尚不清楚。为了在DYT - TOR1A基因模型中探究这些分子途径,我们对幼年小鼠进行了激光显微切割,以分离纹状体胆碱能中间神经元和在成熟过程中主要由棘状投射神经元组成的非胆碱能纹状体组织。富含胆碱能和GABA能的样本均显示出一组明确的基因表达变化,这与扭转蛋白A在分泌途径中的作用一致。富含GABA能的纹状体样本还显示出调节突触传递的基因发生改变,以及活性依赖性即早基因上调。对成年小鼠高尔基-考克斯染色的纹状体棘状投射神经元进行重建,结果显示棘突密度显著增加,这表明扭转蛋白A缺失的纹状体神经元在纹状体成熟过程中兴奋性增加,且传入输入持续增加。这些发现与扭转蛋白A在分泌途径中的发育作用一致,并将扭转蛋白A功能丧失与纹状体胆碱能和GABA能神经元的功能及结构变化联系起来。这些转录组数据集可免费获取,作为未来研究扭转蛋白A功能丧失介导的纹状体功能障碍的资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8127/9980434/09008eb510b9/nihms-1875604-f0001.jpg

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