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Tau 蛋白表达增加与人类大脑皮质发育中的神经元成熟相关。

Increased Tau Expression Correlates with Neuronal Maturation in the Developing Human Cerebral Cortex.

机构信息

Department of Pathology, University of Iowa, Iowa City, IA 52242.

Department of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY 10029.

出版信息

eNeuro. 2020 May 28;7(3). doi: 10.1523/ENEURO.0058-20.2020. Print 2020 May/Jun.

Abstract

Although best known for its role in Alzheimer's disease (AD), tau is expressed throughout brain development, although it remains unclear when and which cell types this expression occurs and how it affects disease states in both fetal and neonatal periods. We thus sought to map tau mRNA and protein expression in the developing human brain at the cellular level using a combination of existing single-cell RNA sequencing (sc-RNAseq) data, RNA hybridization (RNAscope), and immunohistochemistry (IHC). Using sc-RNAseq, we found that tau mRNA expression begins in radial glia but increases dramatically as migrating neuronal precursors mature. Specifically, maturing neurons and mature neurons showed significantly higher mRNA expression than / radial glia or intermediate progenitors. By RNAscope, we found low levels of tau mRNA in subventricular zone (SVZ) radial glia and deep white matter intermediate progenitors, with an increase in more superficially located maturing and mature neurons. By total-tau IHC, the germinal matrix and SVZ showed little protein expression, although both RNAscope and sc-RNAseq showed mRNA, and Western blotting revealed significantly less protein in those areas compared with more mature regions. Induced pluripotent stem cell (iPSC)-derived cortical organoids showed a similar tau expression pattern by sc-RNAseq and RNAscope. Our results indicate that tau increases with neuronal maturation in both the developing fetal brain and iPSC-derived organoids and forms a basis for future research on regulatory mechanisms triggering the onset of tau gene transcription and translation, which may represent potential therapeutic targets for neurodegenerative tauopathies and neurodevelopmental disorders.

摘要

尽管 tau 蛋白以其在阿尔茨海默病(AD)中的作用而闻名,但它在大脑发育过程中广泛表达,尽管目前尚不清楚这种表达发生在何时以及哪些细胞类型中,以及它如何影响胎儿和新生儿期的疾病状态。因此,我们试图在细胞水平上使用现有的单细胞 RNA 测序(sc-RNAseq)数据、RNA 杂交(RNAscope)和免疫组织化学(IHC)来绘制发育中人类大脑中的 tau mRNA 和蛋白表达图谱。使用 sc-RNAseq,我们发现 tau mRNA 表达始于放射状胶质细胞,但随着迁移神经元前体的成熟而急剧增加。具体而言,成熟神经元和成熟神经元的 mRNA 表达显著高于放射状胶质细胞或中间祖细胞。通过 RNAscope,我们发现 SVZ 放射状胶质细胞和深部白质中间祖细胞中的 tau mRNA 水平较低,而成熟和成熟神经元的表达水平逐渐升高。通过总 tau IHC,生发基质和 SVZ 显示出很少的蛋白表达,尽管 RNAscope 和 sc-RNAseq 均显示出 mRNA,Western blot 显示与更成熟区域相比,这些区域的蛋白表达明显较少。诱导多能干细胞(iPSC)衍生的皮质类器官通过 sc-RNAseq 和 RNAscope 显示出相似的 tau 表达模式。我们的结果表明,tau 蛋白在发育中的胎儿大脑和 iPSC 衍生的类器官中随着神经元的成熟而增加,为研究触发 tau 基因转录和翻译的调控机制奠定了基础,这可能是神经退行性 tau 病和神经发育障碍的潜在治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8c5/7262004/cd5f8e5dacc0/SN-ENUJ200129F006.jpg

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