Suppr超能文献

神经元标志物NeuN在小鼠小脑中的发育及细胞类型特异性表达。

Developmental and cell type-specific expression of the neuronal marker NeuN in the murine cerebellum.

作者信息

Weyer Anja, Schilling Karl

机构信息

Anatomisches Institut, Anatomie und Zellbiologie, Rheinische Friedrich-Wilhelms-Universität, Bonn, Germany.

出版信息

J Neurosci Res. 2003 Aug 1;73(3):400-9. doi: 10.1002/jnr.10655.

Abstract

NeuN is a 46/48-kD nuclear protein antigen used widely to identify postmitotic neurons in both research and diagnostics. It is expressed by neurons throughout the nervous system of a variety of species, including birds, rodents, and man (Mullen et al. [1992] Development 116:201-211). When we sought to use NeuN to follow the developmental progression of murine cerebellar interneurons, we observed that expression of this antigen in the cerebellum was restricted to granule neurons and a small population of cells present in the lower molecular layer of the adult cerebellum. In an attempt to identify these cells, we combined immunostaining for NeuN with a panel of cell type-specific markers to unambiguously identify neurons that express NeuN in the adult and developing cerebellum. In contrast to postmitotic granule neurons, NeuN was not expressed by any other immunocytochemically identified cerebellar interneurons, which comprised basket and stellate cells, Golgi neurons, unipolar brush cells, and Lugaro cells. NeuN-positive cells in the molecular layer failed to express any cell type-specific markers tested. They may represent ectopic granule cells; alternatively, they may represent a hitherto unknown population of cerebellar cells. In vitro experiments suggest that NeuN expression is related closely to granule cell axogenesis. This approach also revealed that the level of NeuN expression could be modulated by chronically depolarizing these cells. Thus, whereas NeuN expression per se is a reliable marker of proliferative capacity, levels of NeuN expression may also be indicative of the physiological status of a postmitotic neuron.

摘要

NeuN是一种46/48-kD的核蛋白抗原,在研究和诊断中广泛用于识别有丝分裂后的神经元。它在包括鸟类、啮齿动物和人类在内的多种物种的整个神经系统中的神经元中表达(Mullen等人,[1992]《发育》116:201 - 211)。当我们试图用NeuN追踪小鼠小脑中间神经元的发育进程时,我们观察到该抗原在小脑中的表达仅限于颗粒神经元以及成年小脑分子层下部存在的一小部分细胞。为了识别这些细胞,我们将NeuN免疫染色与一组细胞类型特异性标志物相结合,以明确识别成年和发育中小脑中表达NeuN的神经元。与有丝分裂后的颗粒神经元不同,NeuN在任何其他通过免疫细胞化学鉴定的小脑中间神经元中均不表达,这些中间神经元包括篮状细胞和星状细胞、高尔基神经元、单极刷状细胞和卢加罗细胞。分子层中NeuN阳性细胞未能表达所测试的任何细胞类型特异性标志物。它们可能代表异位颗粒细胞;或者,它们可能代表迄今未知的小脑细胞群体。体外实验表明,NeuN的表达与颗粒细胞轴突形成密切相关。这种方法还揭示,通过长期使这些细胞去极化,可以调节NeuN的表达水平。因此,虽然NeuN表达本身是增殖能力的可靠标志物,但NeuN的表达水平也可能指示有丝分裂后神经元的生理状态。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验